239 results on '"Livingston, Robert"'
Search Results
2. Railway Postal Car A328
- Author
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Livingston, Robert
- Published
- 2006
3. How to Promote Racial Equity in the Workplace.
- Author
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LIVINGSTON, ROBERT
- Subjects
RACIAL inequality ,WORK environment ,RACISM ,ROOT cause analysis ,EMPATHY ,STRATEGIC planning ,EMPLOYMENT discrimination ,RACE discrimination - Abstract
Many White people deny the existence of racism against people of color because they assume that racism is defined by deliberate actions motivated by malice and hatred. However, racism can occur without conscious awareness or intent. When defined simply as differential evaluation or treatment based solely on race, regardless of intent, racism occurs far more frequently than most White people suspect. As intractable as it seems, racism in the workplace can be effectively addressed. Because organizations are small, autonomous entities that afford leaders a high level of control over norms and policies, they are ideal sites for promoting racial equity. Companies should move through the five stages of a process called PRESS: (1) Problem awareness, (2) Root-cause analysis, (3) Empathy, or level of concern about the problem and the people it afflicts, (4) Strategies for addressing the problem, and (5) Sacrifice, or willingness to invest the time, energy, and resources necessary for strategy implementation. [ABSTRACT FROM AUTHOR]
- Published
- 2021
4. How to Promote Racial Equity in the Workplace.
- Author
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Livingston, Robert
- Subjects
PREVENTION of racism ,RACISM in the workplace ,RACISM ,PERSONNEL management ,EMPATHY ,SOCIAL problems ,SOCIAL change - Abstract
Many White people deny the existence of racism against people of color because they assume that racism is defined by deliberate actions motivated by malice and hatred. However, racism can occur without conscious awareness or intent. When defined simply as differential evaluation or treatment based solely on race, regardless of intent, racism occurs far more frequently than most White people suspect. As intractable as it seems, racism in the workplace can be effectively addressed. Because organizations are small, autonomous entities that afford leaders a high level of control over norms and policies, they are ideal sites for promoting racial equity. Companies should move through the five stages of a process called PRESS: (1) Problem awareness, (2) Root-cause analysis, (3) Empathy, or level of concern about the problem and the people it afflicts, (4) Strategies for addressing the problem, and (5) Sacrifice, or willingness to invest the time, energy, and resources necessary for strategy implementation. [ABSTRACT FROM AUTHOR]
- Published
- 2020
5. Clinical Performance Characteristics of the Swift Normalase Amplicon Panel for Sensitive Recovery of Severe Acute Respiratory Syndrome Coronavirus 2 Genomes
- Author
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Shrestha, Lasata, Lin, Michelle J., Xie, Hong, Mills, Margaret G., Mohamed Bakhash, Shah A., Gaur, Vinod P., Livingston, Robert J., Castor, Jared, Bruce, Emily A., Botten, Jason W., Huang, Meei-Li, Jerome, Keith R., Greninger, Alexander L., and Roychoudhury, Pavitra
- Abstract
Amplicon-based sequencing methods are central in characterizing the diversity, transmission, and evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), but need to be rigorously assessed for clinical utility. Herein, we validated the Swift Biosciences' SARS-CoV-2 Swift Normalase Amplicon Panels using remnant clinical specimens. High-quality genomes meeting our established library and sequence quality criteria were recovered from positive specimens, with 95% limit of detection of 40.08 SARS-CoV-2 copies/PCR. Breadth of genome recovery was evaluated across a range of CTvalues (11.3 to 36.7; median, 21.6). Of 428 positive samples, 413 (96.5%) generated genomes with <10% unknown bases, with a mean genome coverage of 13,545× ± SD 8382×. No genomes were recovered from PCR-negative specimens (n = 30) or from specimens positive for non–SARS-CoV-2 respiratory viruses (n = 20). Compared with whole-genome shotgun metagenomic sequencing (n = 14) or Sanger sequencing for the spike gene (n = 11), pairwise identity between consensus sequences was 100% in all cases, with highly concordant allele frequencies (R2 = 0.99) between Swift and shotgun libraries. When samples from different clades were mixed at varying ratios, expected variants were detected even in 1:99 mixtures. When deployed as a clinical test, 268 tests were performed in the first 23 weeks, with a median turnaround time of 11 days, ordered primarily for outbreak investigations and infection control.
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- 2022
- Full Text
- View/download PDF
6. External beam irradiation and the combination of cisplatin and carmustine followed by carmustine alone for the treatment of high-grade glioma: a phase 2 Southwest Oncology Group Trial
- Author
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Blumenthal, Deborah T., Rankin, Cathryn, Eyre, Harmon J., Livingston, Robert B., Spence, Alexander M., Stelzer, Keith J., Rushing, Elisabeth J., Berger, Mitchel S., Rivkin, Saul E., Cohn, Allen L., and Petersdorf, Stephen H.
- Subjects
Cisplatin -- Dosage and administration ,Cisplatin -- Research ,Carmustine -- Dosage and administration ,Carmustine -- Research ,Gliomas -- Care and treatment ,Gliomas -- Research ,Radiotherapy -- Patient outcomes ,Radiotherapy -- Research ,Health - Published
- 2008
7. Diagnosing and Treating Breast Cancer in Elderly Women: A Call for Improved Understanding
- Author
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Downey, Leona, Livingston, Robert, and Stopeck, Alison
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Cancer -- Care and treatment ,Cancer -- Health aspects ,Aged -- Health aspects ,Breast cancer -- Diagnosis ,Breast cancer -- Health aspects ,Knowledge-based system ,Health ,Seniors - Abstract
To purchase or authenticate to the full-text of this article, please visit this link: http://dx.doi.org/10.1111/j.1532-5415.2007.01369.x Byline: Leona Downey (*), Robert Livingston (*), Alison Stopeck (*) Keywords: breast; cancer; diagnosis; treatment; elderly Abstract: Breast cancer is the most common nondermatological malignancy in women, and the incidence increases with age until the eighth decade. Breast cancer pathology and biology appear to be different in elderly patients than in younger ones, and therefore treatment recommendations cannot be generalized from one group to the other. Most elderly women can tolerate breast cancer surgery without significant complications and should be offered a definitive surgical procedure. Improved mechanisms to predict which patients will tolerate and benefit from various therapies are under development. Because most breast cancers in the elderly are hormone responsive, hormonal therapy remains the mainstay of systemic treatment in the adjuvant and metastatic settings. Chemotherapy can be used in elderly women, but treatment decisions must be individualized based upon risk-benefit analyses. Elder-specific studies are underway to identify the most-efficacious and best-tolerated therapies for breast cancer in this population. Primary care physicians must be aware of these issues to provide adequate counseling and care to these patients. Author Affiliation: (*)Section of Hematology and Oncology, University of Arizona, Arizona Cancer Center, Tucson, Arizona Article note: Address correspondence to Leona B. Downey, MD, 1515 N Campbell Ave, Tucson, AZ 85724. E-mail: ldowney@email.arizona.edu
- Published
- 2007
8. [p27.sup.KiP1] and cyclin E expression and breast cancer survival after treatment with adjuvant chemotherapy
- Author
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Porter, Peggy L., Barlow, William E., Yeh, I-Tien, Lin, Ming Gang, Yuan, Xiaopu P., Donato, Elizabeth, Sledge, George W., Shapiro, Charles L., Ingle, James N., Haskell, Charles M., Albain, Kathy S., Roberts, James M., Livingston, Robert B., and Hayes, Daniel F.
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Breast cancer -- Patient outcomes ,Breast cancer -- Research ,Cancer -- Adjuvant treatment ,Cancer -- Patient outcomes ,Cancer -- Research ,Health - Abstract
Background: Abnormal expression of the cell cycle regulatory proteins [p27.sup.Kip1] (p27) and cyclin E may be associated with breast cancer survival and relapse. We studied these markers in a clinical trial setting with patients with breast cancer treated by a uniform drug regimen so that treatment was not associated with variability in outcome. Methods: We used tissue microarrays to evaluate the expression of p27 and cyclin E proteins by immunohistochemistry in tumor tissue from 2123 (68%) of 3122 patients with moderate-risk primary breast cancer who were enrolled in Southwest Oncology Group--Intergroup Trial $9313, in which patients were assigned to receive doxorubicin and cyclophosphamide administered concurrently (n = 1595) of sequentially (n = 1527). Disease-free and overall survival were equivalent in the two arms. Expression of the proteins was rated on a scale of 1-7, and the median value was used as the cut point. Log-rank tests and Cox regression analyses were used to assess associations with survival. Overall survival was defined as time to death from all causes; disease-free survival was defined as time to recurrence of death. All P values were from two-sided statistical tests. Results: Lower p27 expression was associated with worse overall survival (unadjusted hazard ratio [HR] = 1.50, 95% confidence interval [CI] = 1.21 to 1.86) and disease-free survival (unadjusted HR = 1.31, 95% CI = 1.10 to 1.57) than higher p27 expression. Among hormone receptor--positive patients, lower p27 expression was associated with worse overall survival (HR = 1.42, 95% CI = 1.05 to 1.94) and worse disease-free survival (HR = 1.27, 95% CI = 0.99 to 1.63) than higher p27 expression after adjustment for treatment, menopausal status, tumor size, and number of positive lymph nodes. Among these patients, 5-year overall survival associated with higher p27 expression (0.91, 95% CI = 0.89 to 0.93) was similar to that associated with lower p27 expression (0.85, 95% CI = 0.82 to 0.87). No association between p27 expression and survival was found in hormone receptor--negative patients. Cyclin E expression was not statistically significantly associated with overall survival (HR = 1.12, 95% CI = 0.91 to 1.38) or disease-free survival (HR = 1.09, 95% CI = 0.92 to 1.29). Conclusions: Low p27 expression appears to be associated with poor prognosis, especially among patients with steroid receptor--positive tumors.
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- 2006
9. Genomic regions exhibiting positive selection identified from dense genotype data
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Carlson, Christopher S., Thomas Daryl J., Eberle, Michael A., Swanson, Johanna E., Livingston, Robert J., Rieder Mark J., and Nickerson Deborah A.
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Genetic polymorphisms -- Research ,Genotype -- Research ,Human genome -- Research ,Health - Abstract
A significant correlation, was found, between the Tajima's D test statistic in full resequencing data and Tajima's D in a dense, genome-wide data set of genotyped polymorphisms for a set of 179 genes. Identification of the functional polymorphism (and/or halpotype) responsible for the selective sweeps within each CRTR may provide interesting insights into the strongest selective pressures experienced by the human genome.
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- 2005
10. Randomized trial of letrozole following tamoxifen as extended adjuvant therapy in receptor-positive breast cancer: updated findings from NCIC CTG MA.17
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Goss, Paul E., Ingle, James N., Martino, Silvana, Robert, Nicholas J., Muss, Hyman B., Piccart, Martine J., Castiglione, Monica, Tu, Dongsheng, Shepherd, Lois E., Pritchard, Kathleen I., Livingston, Robert B., Davidson, Nancy E., Norton, Larry, Perez, Edith A., Abrams, Jeffrey S., Cameron, David A., Palmer, Michael J., and Pater, Joseph L.
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Tamoxifen -- Dosage and administration ,Breast cancer -- Diagnosis ,Breast cancer -- Drug therapy ,Health - Abstract
Background: Most recurrences in women with breast cancer receiving 5 years of adjuvant tamoxifen occur after 5 years. The MA.17 trial, which was designed to determine whether extended adjuvant therapy with the aromatase inhibitor letrozole after tamoxifen reduces the risk of such late recurrences, was stopped early after an interim analysis showed that letrozole improved disease-free survival. This report presents updated findings from the trial. Methods: Postmenopausal women completing 5 years of tamoxifen treatment were randomly assigned to a planned 5 years of letrozole (n = 2593) or placebo (n = 2594). The primary endpoint was disease-free survival (DFS); secondary endpoints included distant disease-free survival, overall survival, incidence of contralateral tumors, and toxic effects. Survival was examined using Kaplan-Meier analysis and log-rank tests. Planned subgroup analyses included those by axillary lymph node status. All statistical tests were two-sided. Results: After a median follow-up of 30 months (range = 1.5-61.4 months), women in the letrozole arm had statistically significantly better DFS and distant DFS than women in the placebo arm (DFS: hazard ratio [HR] for recurrence or contralateral breast cancer = 0.58, 95% confidence interval [CI] = 0.45 to 0.76; P
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- 2005
11. Residual tumor uptake of [99mTc]-sestamibi after neoadjuvant chemotherapy for locally advanced breast carcinoma predicts survival
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Dunnwald, Lisa K., Gralow, Julie R., Ellis, Georgiana K., Livingston, Robert B., Linden, Hannah M., Lawton, Thomas J., Barlow, William E., Schubert, Erin K., and Mankoff, David A.
- Subjects
Breast cancer -- Research ,Breast cancer -- Care and treatment ,Breast cancer -- Patient outcomes ,Chemotherapy -- Patient outcomes ,Tumors -- Blood-vessels ,Tumors -- Research ,Diagnostic imaging ,Health - Published
- 2005
12. A SPURLESS FORM OF AQUILEGIA CANADENSIS L
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Livingston, Robert B and BioStor
- Published
- 1967
13. Twenty-five years of clinical research for patients with limited-stage small cell lung carcinoma in North America: meaningful improvements in survival
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Janne, Pasi A., Freidlin, Boris, Saxman, Scott, Johnson, David H., Livingston, Robert B., Shepherd, Frances A., and Johnson, Bruce E.
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Lung cancer, Small cell -- Patient outcomes ,Lung cancer, Small cell -- Prognosis ,Health - Published
- 2002
14. Human Immunodeficiency Virus Type 1 (HIV-1) gp120--Specific Antibodies in Neonates Receiving an HIV-1 Recombinant gp120 Vaccine. (Concise Communication)
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McFarland, Elizabeth J., Borkowsky, William, Fenton, Terry, Wara, Diane, McNamara, James, Samson, Pearl, Kang, Minhee, Mofenson, Lynne, Cunningham, Coleen, Duliege, Anne-Marie, Sinangil, Faruk, Spector, Stephen A., Jimenez, Eleanor, Bryson, Yvonne, Burchett, Sandra, Frenkel, Lisa M., Yogev, Ram, Gigliotti, Francis, Luzuriaga, Katherine, and Livingston, Robert A.
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HIV infection in children -- Physiological aspects ,Infants (Newborn) ,Antibodies -- Measurement ,Health - Published
- 2001
15. Combined etoposide, ifosfamide, and cisplatin in the treatment of patients with advanced thymoma and thymic cancer: an intergroup trial
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Loehrer, Patrick J., Jiroutek, Michael, Aisner, Seena, Aisner, Joseph, Green, Mark, Thomas, Charles R., Jr., Livingston, Robert, and Johnson, David H.
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Chemotherapy, Combination -- Evaluation ,Thymoma ,Etoposide -- Health aspects ,Ifosfamide -- Health aspects ,Cisplatin -- Health aspects ,Health - Published
- 2001
16. Increased false negative sentinel node biopsy rates after preoperative chemotherapy for invasive breast carcinoma
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Nason, Katie S., Anderson, Benjamin O., Byrd, David R., Dunnwald, Lisa K., Eary, Janet F., Mankoff, David A., Livingston, Robert, Schmidt, Rodney A., Jewell, Kim D., Yeung, Raymond S., and Moe, Roger E.
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Lymph nodes -- Biopsy ,Breast cancer ,Tumor staging -- Evaluation ,Health - Published
- 2000
17. Similar outcome of elderly patients in Intergroup Trial 0096: cisplatin, etoposide, and thoracic radiotherapy administered once or twice daily in limited stage small cell lung carcinoma
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Yuen, Alan R., Zou, Guangyong, Turrisi, Andrew T., Sause, William, Komaki, Ritsuko, Wagner, Henry, Aisner, Seena C., Livingston, Robert B., Blum, Ronald, and Johnson, David H.
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Lung cancer, Small cell -- Care and treatment ,Aged patients -- Care and treatment ,Health - Published
- 2000
18. The Party's Over: Kohl's Disservice to German Democracy
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Livingston, Robert Gerald
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Germany -- Political aspects ,Political fund raising ,International relations ,Political science ,Christian Democratic Union -- Political aspects -- Political activity -- Personalities - Abstract
Former Chancellor Helmut Kohl's secret, illegal fundraising has corroded the German public's trust in its political parties and in the party-dominated system itself. The revelations that surfaced in late autumn [...]
- Published
- 2000
19. Monitoring the response of patients with locally advanced breast carcinoma to neoadjuvant chemotherapy using [technetium 99m]-sestamibi scintimammography
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Mankoff, David A., Dunnwald, Lisa K., Gralow, Julie R., Ellis, Georgiana K., Drucker, Mariann J., and Livingston, Robert B.
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Breast cancer ,Radioisotope scanning -- Usage ,Technetium -- Isotopes ,Health - Published
- 1999
20. Safety and immunogenicity of HIV recombinant envelope vaccines in HIV-infected infants and children
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Lambert, John S., McNamara, James, Katz, Samuel L., Fenton, Terry, Kang, Minhee, VanCott, Thomas C., Livingston, Robert, Hawkins, Elizabeth, Moye, Jack, Jr., Borkowsky, William, Johnson, Daniel, Yogev, Ram, Duliege, Ann-Marie, Francis, Donald, Gershon, Anne, Wara, Diane, Martin, Natasha, Levin, Myron, McSherry, George, and Smith, Gale
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AIDS vaccines -- Testing ,HIV infection in children -- Prevention ,Health - Abstract
AIDS vaccines made from the HIV gp120 or gp 160 protein appear to be safe enough to use in infants and children. Researchers vaccinated 72 HIV-infected children between one month and 18 years old with a gp120 vaccine, a gp160 vaccine, or a placebo approximately every month for about six months. Sixty-five percent of those who received the vaccine developed an immune response to it, which did not occur in the placebo group.
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- 1998
21. Life after Kohl? We'll Always Have Germany
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Livingston, Robert Gerald
- Subjects
Germany -- Political aspects ,International relations ,Political science - Abstract
'His Eternality' is how the leader of Germany's Greens once referred to him. Indeed, Helmut Kohl has led his country for 15 years, the longest tenure of any chancellor this [...]
- Published
- 1997
22. Teniposide (VM-26) as a single drug treatment for patients with extensive small cell lung carcinoma: a Phase II study of the Southwest Oncology Group
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Grozea, Petre N., Crowley, John J., Canfield, Vikki A., Kingsbury, Laura, Ross, S. William, Beltran, German S., Laufman, Leslie Rodgers, Weiss, Geoffrey R., and Livingston, Robert B.
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Lung cancer, Small cell ,Antineoplastic agents -- Evaluation ,Health - Published
- 1997
23. Evaluation of cisplatin, carboplatin, and etoposide in metastatic nonsmall lung carcinoma: a Phase II study of the Southwest Oncology Group
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Figlin, Robert A., Crowley, John J., Jacobs, Edwin L., Muirhead, Michael, Goodwin, John Wendall, Rinehart, John J., and Livingston, Robert B.
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Lung cancer, Non-small cell ,Chemotherapy, Combination -- Evaluation ,Health - Published
- 1996
24. Treatment of malignant mesothelioma with methotrexate and vinblastine, with or without platinum chemotherapy
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Hunt, Karen J., Longton, Gary, Williams, Margaret A., and Livingston, Robert B.
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Platinum -- Health aspects -- Evaluation ,Mesothelioma -- Health aspects ,Methotrexate -- Evaluation ,Chemotherapy -- Health aspects ,Vinblastine -- Evaluation ,Chemotherapy, Combination -- Evaluation -- Health aspects ,Cancer -- Chemotherapy ,Health ,Evaluation ,Health aspects - Abstract
Study objective: To determine the efficacy of methotrexate, vinblastine, and platinum chemotherapy in patients with diffuse unresectable malignant mesothelioma. Design: Patients with histologically confirmed malignant mesothelioma were evaluated for treatment [...]
- Published
- 1996
25. Human immunodeficiency virus-specific IgA in infants born to human immunodeficiency virus-seropositive women
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Livingston, Robert A., Hutton, Nancy, Halsey, Neal A., Kline, Richard L., Joyner, Mary, and Quinn, Thomas C.
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HIV infection ,Immunoglobulin A -- Measurement ,Maternal-fetal exchange -- Physiological aspects ,Health - Abstract
Objective: To determine the sensitivity and specificity of human immunodeficiency virus (HIV)-specific IgA for vertically transmitted HIV infection, particularly during the first month of life. Design/Setting/Patients: Prospective cohort study of 140 infants born to HIV-seropositive women in a large urban teaching hospital and of 248 older infants and children referred for diagnosis and treatment of HIV infection. Main Outcome Measures: The HIV-specific IgA immunoblot results were compared with the infection status of patients as determined by Centers for Disease Control and Prevention (Atlanta, Ga) criteria or by sequential early diagnostic assays for HIV. Sensitivity, specificity, and predictive values were calculated for each age range. Results: Among infants studied from birth, the rate of vertical transmission of HIV was 21.6% (25/116). The sensitivity of HIV-specific IgA for the first month of life was 8.0% (2/25), and the specificity was 90.1% (82/91). Sensitivity increased progressively during the first year of life, and the negative predictive value was 94.6% by 6 to 8 months of age. The positive predictive value of this assay was 18.2% for neonates but was 96% to 100% after the first month of life. Conclusions: False-positive test results for HIV-specific IgA occurred with diminishing frequency during the first 4 weeks of life, and the frequency of detectable HIV-specific IgA was similar among the HIV-infected and uninfected groups at this age. Beyond 1 month of age, detection of HIV-specific IgA is highly specific and is a useful serum-based assay for early diagnosis of HIV infection. These results suggest that maternal-fetal transfusion is common and support the hypothesis that the majority of maternal-fetal transmission of HIV occurs around the time of parturition., Finding HIV-specific immunoglobulin A (IgA) in the blood of infants born to HIV-infected mothers appears to be highly predictive of HIV infection but only after the first month of life. Of 116 infants born to HIV-positive women who were tested an average of 12 days after birth, 22% were infected. In the first month of life 2 of these 25 infants tested positive for HIV-specific IgA and 10% of infants had false-positive tests. By four weeks of age, the false-positive rate fell to zero. This suggests that maternal IgA is transmitted to the baby around the time of birth. The presence of HIV-specific IgA accurately identifies 96% to 100% of HIV-infected infants after the first month of life.
- Published
- 1995
26. Longitudinal assessment of growth in children born to mothers with human immunodeficiency virus infection
- Author
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Saavedra, Jose M., Henderson, Robin A., Perman, Jay A., Hutton, Nancy, Livingston, Robert A., and Yolken, Robert H.
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Children -- Growth ,HIV infection in children -- Health aspects ,Health - Abstract
Objectives: To describe and to evaluate the longitudinal growth of children born to mothers with human immunodeficiency virus (HIV) infection. Design: Measurements of weight, length (measured in infants in a recumbent position) and height (measured in older children in an upright position), and head circumference were documented and evaluated longitudinally using generalized estimating equations in a group of children born to HIV-infected mothers. Children infected with HIV were compared with uninfected children and with National Center for Health Statistics standards. Setting: Primary care clinic in an urban hospital devoted to the medical care of children born to HIV-infected mothers. Patients: One hundred nine children born to HIV-infected mothers, 59 HIV-infected and 50 uninfected, between birth and 70 months of age. Results: The mean birth weights of both groups were below the 50th percentile. While the mean weight-for-age curve of uninfected children attained the 50th percentile by age 24 months, the mean birth weight-for-age curve of HIV-infected children remained below the 50th percentile. Weight gain became significantly different between the two groups by age 36 months. The mean birth length-for-age curves of HIV-infected and uninfected children was also below the 50th percentile. The mean height-for-age curve of uninfected children attained the 50th percentile by age 40 months, while that of HIV-infected children remained well below the 50th percentile. Linear growth between HIV-infected and uninfected children diverged earlier than weight, becoming significantly different by age 15 months. Conclusions: Although children born to HIV-infected mothers are born with weight and length below the 50th percentile, uninfected children catch up, while HIV-infected children remain below the 50th percentile and experience an earlier and more pronounced decrease in linear growth (height-for-age) than in weight-for-age. (Arch Pediatr Adolesc Med. 1995;149:497-502), Babies born to HIV-infected mothers may be smaller and weigh less than average for their age and those who are infected remain so. Researchers periodically measured weight, length, and head circumference on 109 children born to HIV-infected mothers between birth and 70 months. Fifty-nine children were infected with HIV. Average birth weights of both infected and non-infected children were below the 50th percentile for the general population. However, uninfected children achieved the 50th percentile for weight by 24 months old, whereas HIV-infected children remained below the 50th percentile. Length-for-age was also below the 50th percentile in both groups. By 40 months the uninfected children had achieved the 50th percentile for height, but HIV-infected children remained below the 50th percentile.
- Published
- 1995
27. Radiation Therapy Oncology Group (RTOG) 88-08 and Eastern Cooperative Oncology Group (ECOG) 4588: preliminary results of a phase III trial in regionally advanced unresectable non-small-cell lung cancer
- Author
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Sause, William T., Scott, Charles, Taylor, Samuel, Johnson, David, Livingston, Robert, Komaki, Ritsuko, Emami, Bahman, Curran, Walter J., Byhardt, Roger W., Turrisi, Andrew T., Dar, A. Rashid, and Cox, James D.
- Subjects
Lung cancer, Non-small cell -- Radiotherapy ,Radiotherapy -- Usage ,Health - Abstract
Background: Regionally advanced, surgically unresectable non-small-cell lung cancer represents a disease with an extremely poor prognosis. External-beam irradiation to the primary tumor and regional lymphatics is generally accepted as standard therapy. The use of more aggressive radiation regimens and the addition of cytotoxic chemotherapy to radiotherapy have yielded conflicting results. Recently, however, results from clinical trials using innovative irradiation delivery techniques or chemotherapy before irradiation have indicated that patients treated with protocols that incorporate these modifications may have higher survival rates than patients receiving standard radiation therapy. Purpose: On the basis of these results, the Radiation Therapy Oncology Group RTOG)-Eastern Cooperative Oncology Group (ECOG) elected to conduct a phase III trial comparing the following regimens: 1) standard radiation therapy, 2) induction chemotherapy followed by standard radiation therapy, and 3) twice-daily radiation therapy. Methods: Patients with surgically unresectable stage II, IIIA, or IIIB non-small-cell lung cancer were potential candidates. Staging was nonsurgical. Patients were required to have a Karnofsky performance status of 70 or more and weight loss less than 5% for 3 months prior to entry into the trial, to be older than 18 years of age, and to have no metastatic disease. Of the 490 patients registered in the trial, 452 were eligible. The disease in 95% of the patients was stage IIIA or IIIB. More than two thirds of the patients had a Karnofsky performance status of more than 80. Patients were randomly assigned to receive either 60 Gy of radiation therapy delivered at 2 Gy per fraction, 5 days a week, over a 6-week period (standard radiation therapy); induction chemotherapy consisting of cisplatin (100 mg/m[sup.2]) on days 1 and 29 and 5 mg/m[sup.2] vinblastine per week for 5 consecutive weeks beginning on day 1 with cisplatin, followed by standard radiation therapy starting on day 50; or 69.6 Gy delivered at 1.2 Gy per fraction twice daily (hyperfractionated radiation therapy). Results: Toxicity was acceptable, with four treatment-related deaths. Three patients subsequently died of chronic pulmonary complications. Compliance with protocol treatment was acceptable. One-year survival (%) and median survival (months) were as follows: standard radiation therapy - 46%, 11.4 months; chemotherapy plus radiotherapy - 60%, 13.8 months; and hyperfractionated radiation therapy - 51%, 12.3 months. The chemotherapy plus radiotherapy arm was statistically superior to the other two treatment arms (logrank P = .03). Conclusions: In 'good-risk' patients with surgically unresectable non-small-cell lung cancer, induction chemotherapy followed by irradiation was superior to hyperfractionated radiation therapy or standard radiation therapy alone, yielding a statistically significant short-term survival advantage.
- Published
- 1995
28. Dose intensity and high dose therapy: two different concepts
- Author
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Livingston, Robert B.
- Subjects
Breast cancer ,Chemotherapy -- Management ,Health - Abstract
'Dose response' refers to a direct relationship between the amount of chemotherapy administered and observed degree of antitumor effect. What is often implied by the term is the administration of pulsed, high dose therapy, resulting, in very high peak concentrations. Clinically, this has been translated as multiple alkylating agent-based regimens requiring intensive supportive care and associated with substantial morbidity and an appreciable mortality risk. Such regimens typically are given as consolidation after an initial period of standard outpatient therapy and may require autologous hematopoietic stem cell support. 'Dose intensity' is defined as the amount of drug administered per unit of time, typically reported in mg/[m.sup.2]/ week. This is a more precise term than 'dose response.' A dose-intensive regimen may or may not be one associated with high peak concentrations. For example, prolonged or continuous administration of an agent like cyclophosphamide may be quite dose-intensive, but will be associated with lower peak concentrations and less acute toxicity than a similarly dose-intensive, pulsed high dose regimen of the same drug. Retrospective analyses and prospective, randomized trials suggest the importance of dose intensity in the treatment of breast cancer. The evidence that high dose therapy (associated with high pea k plasma levels) is beneficial in breast cancer rests on a number of Phase II trials. In the setting of poor prognosis Stage IV disease, these trials suggest little improvement in median survival, but better long term survival (at or beyond 2 years) in 15-25% of such patients. This benifiting cohort appears to be in unmaintained disease free remission, whereas standard therapy in the past has almost never produced such remissions in the poor prognosis subgroup of Stage IV disease. In the setting of high risk Stage II disease, Phase II trials of similar high dose therapy indicate a higher proportion of patients who are free of recurrence at 2-3 years than expected from available historic controls. Randomized trials are now underway in Stage IV poor prognosis patients and in Stage II high risk patients to see whether the apparent improvements in outcome associated with pulsed high dose chemotherapy can be validated prospectively. The regimens under study in these randomized trials include agents that require autologous support with harvested bone marrow and/or peripheral blood progenitor cells. Such obligate stem cell support carries with it the risk of tumor cell contamination in the collection and subsequent iatrogenic dissemination of disease. The frequency and magnitude of this contamination are under study, and methods to purge the autologous collection of tumor cells are under development, but both types of research are embryonic. Alternative approaches to pulsed, high dose chemotherapy not requiring autologous stem cell support exist, and reported results in poor prognosis Stage IV disease appear comparable to those achieved by obligate stem cell programs. Development of genetically engineered hematopoietic growth factors has facilitated approaches to improved dose intensity as well as to pulsed high dose consolidation. Thrombocytopenia and mucositis, however, are little affected by the available growth factors. Further improvements in therapeutic index for both approaches may result from new growth factors now under study. The use of peripheral blood progenitor cells shortens thrombocytopenia after high dose regimens. A new area of investigation involves the suppression of negative regulators of hematopoiesis (e.g., tumor necrosis factor), which may be overexpressed after bone marrow injury by high dose therapy. The future may involve combining concepts of dose response (e.g., dose intensive induction to pulsed consolidation). Optimal results are likely to be achieved through the integration of dose response with other approaches (local irradiation to high risk sites, biologic response modifiers). Cancer 1994; 74:1177-83. Key words: dose intensity, dose response, peak dose level, breast cancer, hematopoietic growth factors.
- Published
- 1994
29. Predictors of survival following relapse or progression of small cell lung cancer: Southwest Oncology Group study 8605 report and analysis of recurrent disease data base
- Author
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Albain, Kathy S., Crowley, John J., Hutchins, Laura, Gandara, David, O'Bryan, Robert M., Von Hoff, Daniel D., Griffin, Brian, and Livingston, Robert B.
- Subjects
Lung cancer, Small cell -- Patient outcomes ,Cancer -- Relapse ,Cancer survivors -- Research ,Health - Abstract
Background. Survival after relapse or progression of small cell lung cancer (SCLC) is poor. The Southwest Oncology Group (SWOG) initiated a study of modulation of cyclophosphamide (Cy) resistance in this population. At study closure, the value of testing new regimens in previously treated patients was being debated nationally: Is there an independent impact of treatment over favorable prognostic factors? Thus, the authors analyzed the SWOG recurrent SCLC data base. Methods. A 12-hour infusion of cytosine arabinoside (ara-C) was used as a potential repair inhibitor of Cy-induced DNA damage in patients with relapsed SCLC. A data base of successive SWOG studies in recurrent SCLC was formed. The independent contribution to survival of prognostic factors, type of prior chemotherapy (CT), time from diagnosis, and type of CT on relapse were then assessed. Results. There were 3 partial responses observed in 67 patients, with substantial myelotoxicity. The median survival was 2.5 months, and 16% lived beyond 6 months. The multivariate analysis of the recurrent SCLC data base found that a normal lactate dehydrogenase (LDH) and second-line treatment with etoposide plus cisplatin (EP), if not initially treated with either alternating or complex multidrug regimens, were the only independent predictors of improved survival. The 2-year survival of this subset was 20%. Conclusions. The Cy/ara-C program cannot be recommended for patients with recurrent SCLC. However, EP independently contributed to improved survival in patients without complex prior CT and a normal LDH. This finding supports future trials of new approaches in certain subsets of SCLC patients with limited prior treatment. Cancer 1993; 72:1184-91.
- Published
- 1993
30. Prolonged, alternating chemotherapy for extensive small cell lung cancer: a Southwest Oncology Group Study
- Author
-
Livingston, Robert B., Crowley, John J., Thompson, Tove, Williamson, Stephen K., Meyers, Frederick J., O'Rourke, Timothy, and Neefe, John R.
- Subjects
Lung cancer, Small cell ,Chemotherapy, Combination -- Dosage and administration ,Health - Abstract
Background. Etoposide may be schedule dependent in small cell lung cancer (SCLC), and some data suggest a benefit for increased dose intensity in this disease. This study attempted to optimize dose intensity using an out-patient program that included prolonged, oral etoposide administration. Methods. Cisplatin-etoposide (PE) and cyclophosphamide, doxorubicin, and vincristine (CAV) were alternated at monthly intervals in patients with extensive SCLC. PE was given as cisplatin 50 mg/[m.sup.2] on days 1 and 8 intravenously (IV) and etoposide 50 mg/[m.sup.2]/day for 14 days by mouth. CAV was administered as cyclophosphamide 60 mg/[m.sup.2]/day for 21 days orally, doxorubicin 20 mg/[m.sup.2]/week for three doses, and vincristine 2 mg IV on day 1 only. At the end of 4 months, responding patients received an additional course of PE alternating with CAV, and whole-brain irradiation (3000 cGy in 15 fractions) was delivered to clinical complete responders (CR). Results. Among 61 eligible patients, 4 achieved CR, and 11 had a partial remission, by strict Southwest Oncology Group criteria. An additional 20 patients demonstrated greater than 50% tumor shrinkage on one disease assessment but did not have confirming measurements at all sites 4 weeks later. The overall response rate was 57%, including the latter group. The toxicity was primarily hematologic, with three treatment-related deaths from neutropenic infection (5%). Grade 4 neutropenia (< 500/[mu]l) occurred in nine patients (15%) and Grade 4 thrombocytopenia (< 25,000/,[mu]l), in three (5%). Analysis of the delivered dose intensity (in milligrams per square meter per week) as a function of that which was planned revealed a mean of 93% for all courses. Conclusions. Although substitution of prolonged oral etoposide in PE and oral cyclophosphamide in CAV proved to be feasible, these results suggest no advantage over those from other reported series using these alternating regimens in which the agents are pulsed. Experience with alternating PE-CAV for extensive SCLC is reviewed.
- Published
- 1993
31. Feasibility of dose-intensive continuous 5-fluorouracil, doxorubicin, and cyclophosphamide as adjuvant therapy for breast cancer
- Author
-
Ellis, Georgiana and Livingston, Robert B.
- Subjects
Breast cancer -- Adjuvant treatment ,Fluorouracil -- Dosage and administration ,Doxorubicin -- Dosage and administration ,Cyclophosphamide -- Dosage and administration ,Health - Abstract
Background. Several studies support the belief that the efficacy of adjuvant chemotherapy in breast cancer is related to the dose intensity of the chemotherapy used (expressed in milligrams per square meter per week). Retrospective analyses indicate that the actual delivered dose intensity may correlate more strongly with efficacy than the intended dose delivery. Methods. A doxorubicin-based adjuvant regimen was studied for breast cancer. It was modeled on the Southwest Oncology Group's regimen of cyclophosphamide, methotrexate, and 5-fluorouracil in that daily oral cyclophosphamide and weekly intravenous 5-fluorouracil were used, but weekly doxorubicin was substituted for methotrexate and administered in both the adjuvant and neoadjuvant setting to 29 patients. Results. The actual dose delivery was 1.21-1.24-fold that calculated for the delivered dose in the two other adjuvant regimens using the same three drugs (5-fluorouracil, doxorubicin, and cyclophosphamide) for which this could be determined. This regimen was tolerated well. Toxicity was minimal and consisted largely of expected neutropenia. Conclusions. Whether improved dose intensity can be increased further with the use of growth factors or actually confers improved outcomes awaits the results of larger future trials. Cancer 1993; 71:392-6.
- Published
- 1993
32. Cisplatin and novobiocin in the treatment of non-small cell lung cancer: a Southwest Oncology Group study
- Author
-
Ellis, Georgiana K., Crowley, John, Livingston, Robert B., Goodwin, John W., Hutchins, Laura, and Allen, Ace
- Subjects
Antibiotics -- Usage ,Cisplatin -- Evaluation ,Lung cancer ,Health - Abstract
Novobiocin is an antibiotic that works by inhibiting (stopping the action of) a bacterial enzyme involved in the maintenance of DNA (genetic material). Novobiocin also inhibits an enzyme in human cells as well. Experiments in tissue culture have indicated that the inhibition of this enzyme, called DNA topoisomerase II, actually potentiates the action of some anticancer drugs, including cisplatin. In some preliminary studies, it seemed that the addition of novobiocin to chemotherapeutic regimens containing cisplatin might improve the response of lung cancer patients to treatment. As the study involved only a small number of patients, it is important to test this drug combination in a larger and more reliable study. However, the completion of such a study provides no reason to believe that this drug combination provides any useful benefit. A total of 36 patients with non-small cell lung cancer were treated. No complete responses were achieved and only three partial responses were observed. The midpoint survival time of the patients was less than seven months, which is no better than could be achieved using cisplatin alone. At present, novobiocin is available as capsules which are taken orally. Better results might be achieved if it were possible to administer novobiocin to the patients intravenously. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1991
33. Long-term survival and toxicity in small cell lung cancer: expanded Southwest Oncology Group experience
- Author
-
Albain, Kathy S., Crowley, John J., and Livingston, Robert B.
- Subjects
Mortality ,Lung cancer, Small cell -- Patient outcomes -- Prognosis ,Health ,Prognosis ,Patient outcomes - Abstract
Long-term survival free of recurrence following the diagnosis and treatment of small cell lung cancer (SCLC) occurs in a small percentage of patients. It is a matter of lively debate [...]
- Published
- 1991
34. A weekly cisplatin-based induction regimen for extensive non- small cell lung cancer: a Southwest Oncology Group study
- Author
-
Higano, Celestia S., Crowley, John, Livingston, Robert B., Goodwin, John Wendall, Barlogie, Barthel, and Stuckey, W.J.
- Subjects
Lung cancer ,Cisplatin -- Dosage and administration ,Cisplatin -- Evaluation ,Health - Abstract
Much of the current research in chemotherapy for cancer is focused on improving the results obtained with already established chemotherapeutic agents. Cisplatin is one of the more effective chemotherapeutic drugs for the treatment of lung cancer. As is often the case, the effectiveness of the drug is limited by its toxicity. Greater anti-cancer activity could be achieved at higher doses, but the toxic effects of the higher doses would be unacceptable. Researchers have tried to improve upon the success of cisplatin-containing chemotherapeutic regimens in the treatment of non-small cell lung cancer. One approach is that each round of chemotherapy contains cisplatin, but another agent is combined with cisplatin and the identity of this second agent is rotated from round to round. In the present study, cisplatin was administered for eight weeks; the drug was given in combination with mitomycin C on weeks one and six, with vinblastine on weeks two and seven, and in combination with 5-fluorouracil on weeks three and eight. Patients who responded to this treatment regimen were given cisplatin and etoposide for three monthly cycles. Eighty patients were eligible for participation in the study, and 77 were evaluable for their response to treatment. One patient achieved a complete response, and 17 patients achieved partial responses, for an overall response rate of 23 percent. The median survival was 4.6 months. Neither the overall survival rate nor the toxicity of this treatment protocol were significantly different from the standard dose regimens. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1991
35. Chemotherapy for advanced thymoma: preliminary results of an intergroup study
- Author
-
Loehrer, Patrick J., Perez, Carlos Andres, Roth, Lawrence M., Greco, F. Anthony, Livingston, Robert B., and Einhorn, Lawrence H.
- Subjects
Thymoma -- Drug therapy ,Chemotherapy, Combination -- Evaluation ,Health - Abstract
Thymoma is a tumor originating in the epithelial tissues lining the surface of the thymus gland. This gland is located in the mediastinal cavity, the space containing the organs and tissues separating the lungs. The thymus gland is important in the development of the immune response in newborns and is essential to the maturation of T cells, a type of immune cell. The effectiveness of a combined regimen of the anticancer agents cisplatin, doxorubicin, and cyclophosphamide in treating thymoma was assessed in 20 patients. Three patients underwent complete remission, and 11 patients experienced partial remissions. The response rate was estimated at 70 percent. Remission lasted 13 months in most patients, and three patients remained free of disease for more than two years. Most patients survived about 59 months. Infections developed in four patients and included infections of the meninges, the membrane lining the brain and spinal cord; yeast infections of the mucous and skin tissues; and infection of the lung by fungi. The development of infections indicated abnormalities in cell-mediated immunity. These findings indicate that a combined regimen of the chemotherapeutic agents cisplatin, doxorubicin, and cyclophosphamide can produce remission in patients with thymoma. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1990
36. Germany's sunken memories. (In Other Words)
- Author
-
Livingston, Robert Gerald
- Subjects
Crabwalk (Novel) -- Book reviews ,Books -- Book reviews ,International relations ,Political science - Abstract
Im Krebsgang (Crabwalk) By Gunter Grass 216 pages, Gottingen: Steidl Verlag, 2002 (in German) (Forthcoming in English, April 2003, by Harcourt Trade Publishers) History, more precisely that history which we [...]
- Published
- 2003
37. Association Between 21-Gene Assay Recurrence Score and Locoregional Recurrence Rates in Patients With Node-Positive Breast Cancer
- Author
-
Woodward, Wendy A., Barlow, William E., Jagsi, Reshma, Buchholz, Thomas A., Shak, Steven, Baehner, Frederick, Whelan, Timothy J., Davidson, Nancy E., Ingle, James N., King, Tari A., Ravdin, Peter M., Osborne, C. Kent, Tripathy, Debasish, Livingston, Robert B., Gralow, Julie R., Hortobagyi, Gabriel N., Hayes, Daniel F., and Albain, Kathy S.
- Abstract
IMPORTANCE: The 21-gene assay recurrence score is increasingly used to personalize treatment recommendations for systemic therapy in postmenopausal women with estrogen receptor (ER)– or progesterone receptor (PR)–positive, node-positive breast cancer; however, the relevance of the 21-gene assay to radiotherapy decisions remains uncertain. OBJECTIVE: To examine the association between recurrence score and locoregional recurrence (LRR) in a postmenopausal patient population treated with adjuvant chemotherapy followed by tamoxifen or tamoxifen alone. DESIGN, SETTING, AND PARTICIPANTS: This cohort study was a retrospective analysis of the Southwest Oncology Group S8814, a phase 3 randomized clinical trial of postmenopausal women with ER/PR-positive, node-positive breast cancer treated with tamoxifen alone, chemotherapy followed by tamoxifen, or concurrent tamoxifen and chemotherapy. Patients at North American clinical centers were enrolled from June 1989 to July 1995. Medical records from patients with recurrence score information were reviewed for LRR and radiotherapy use. Primary analysis included 316 patients and excluded 37 who received both mastectomy and radiotherapy, 9 who received breast-conserving surgery without documented radiotherapy, and 5 with unknown surgical type. All analyses were performed from January 22, 2016, to August 9, 2019. MAIN OUTCOMES AND MEASURES: The LRR was defined as a recurrence in the breast; chest wall; or axillary, infraclavicular, supraclavicular, or internal mammary lymph nodes. Time to LRR was tested with log-rank tests and Cox proportional hazards regression for multivariate models. RESULTS: The final cohort of this study comprised 316 women with a mean (range) age of 60.4 (44-81) years. Median (interquartile range) follow-up for those without LRR was 8.7 (7.0-10.2) years. Seven LRR events (5.8%) among 121 patients with low recurrence score and 27 LRR events (13.8%) among 195 patients with intermediate or high recurrence score occurred. The estimated 10-year cumulative incidence rates were 9.7% for those with a low recurrence score and 16.5% for the group with intermediate or high recurrence score (P = .02). Among patients who had a mastectomy without radiotherapy (n = 252), the differences in the 10-year actuarial LRR rates remained significant: 7.7 % for the low recurrence score group vs 16.8% for the intermediate or high recurrence score group (P = .03). A multivariable model controlling for randomized treatment, number of positive nodes, and surgical type showed that a higher recurrence score was prognostic for LRR (hazard ratio [HR], 2.36; 95% CI, 1.02-5.45; P = .04). In a subset analysis of patients with a mastectomy and 1 to 3 involved nodes who did not receive radiation therapy, the group with a low recurrence score had a 1.5% rate of LRR, whereas the group with an intermediate or high recurrence score had a 11.1% LRR (P = .051). CONCLUSIONS AND RELEVANCE: This study found that higher recurrence scores were associated with increased LRR after adjustment for treatment, type of surgical procedure, and number of positive nodes. This finding suggests that the recurrence score may be used, along with accepted clinical variables, to assess the risk of LRR during radiotherapy decision-making.
- Published
- 2020
- Full Text
- View/download PDF
38. Tumor masquerading as tendinitis
- Author
-
Livingston, Robert D., Jr.
- Subjects
Tendinitis -- Diagnosis ,Diagnosis, Radioscopic -- Case studies ,Osteoma -- Diagnosis ,Health - Published
- 1993
39. Pattern of sequence variation across 213 environmental response genes
- Author
-
Livingston, Robert J., Niederhausern, Andrew von, Jegga, Anil G., Crawford, Dana C., Carlson, Christopher S., Rieder, Mark J., Gowrisankar, Sivakumar, Aronow, Bruce J., Weiss, Robert B., and Nickerson, Deborah A.
- Subjects
Human genetics -- Research ,Nucleotide sequence -- Research ,Single nucleotide polymorphisms -- Research ,Health - Abstract
The study of one of the most comprehensive sets of gene based SNPs (single nucleotide polymorphisms) assembled is presented. The study provides an important view of the structure of sequence diversity across the human genome and improves understanding of human genetic susceptibility to environmental exposure.
- Published
- 2004
40. Final Results of Phase III Trial in Regionally Advanced Unresectable Non-Small Cell Lung Cancer(*)
- Author
-
Sause, William, Kolesar, Patricia, Taylor, Samuel IV, Johnson, David, Livingston, Robert, Komaki, Ritsuko, Emami, Bahman, Curran, Walter Jr., Byhardt, Roger, Dar, A. Rashid, and Turrisi, Andrew III
- Subjects
Combined modality therapy -- Evaluation ,Lung cancer, Non-small cell -- Care and treatment ,Health ,Care and treatment ,Evaluation - Abstract
Radiation Therapy Oncology Group, Eastern Cooperative Oncology Group, and Southwest Oncology Group Study objectives: The purpose of this phase III clinical trial was to test whether chemotherapy followed by radiation [...]
- Published
- 2000
41. Fixing a Leaky Toilet Tank
- Author
-
Livingston, Robert
- Subjects
Toilets -- Maintenance and repair ,Mirrors -- Maintenance and repair ,Door fittings -- Maintenance and repair ,Sprinkler irrigation -- Maintenance and repair ,Flooring -- Maintenance and repair - Published
- 1999
42. Grandma was drying food before 1889
- Author
-
Livingston, Robert M.
- Subjects
Grandmothers -- Social aspects ,Grandmothers -- Food and nutrition ,Food -- Drying ,Food -- Methods - Abstract
COUNTRYSIDE: The July/August issue was, as usual, a great read! The entire issue. Regarding "Dry it. You'll Like It" (July/August 2008, pg. 54), at age 88, I remember the joys […]
- Published
- 2008
43. Combination chemotherapy and high-dose cyclophosphamide intensification for poor prognosis breast cancer: a Southwest Oncology Group Study
- Author
-
Ellis, Georgiana K., Green, Stephanie, Schulman, Susan, Tranum, Bill L., Goldberg, Ronald S., and Livingston, Robert B.
- Subjects
Cyclophosphamide -- Health aspects ,Breast cancer ,Health - Abstract
Research has provided insights into factors associated with a poor prognosis in breast cancer. One such factor is the absence of the estrogen receptor on breast cancer cells (estrogen-receptor-negative); not only does this factor carry a poor prognosis, but it also correlates with other more traditional negative prognostic factors, such as liver metastases (spread of cancer to the liver). Recurrent or disseminated breast cancers are generally treated with a combination of agents, which usually includes doxorubicin, sometimes referred to by its brand name Adriamycin. Although some response may be achieved in 70 to 80 percent of the patients with estrogen-receptor-negative breast cancer, survival is generally poor with less than 5 percent of patients surviving five years after diagnosis. Roughly 20 percent of patients with estrogen-receptor-positive cancer survive five years after diagnosis. To try to improve treatment success for these poor-prognosis patients, high-dose cyclophosphamide was added to intensify chemotherapy; previous studies established that doses of cyclophosphamide as high as 200 milligrams per kilogram (mg per kg) can be tolerated without necessitating bone marrow infusion. Of 45 patients enrolled in the study, 35 were fully evaluable for results. Patients who continued to have progressive disease after initial chemotherapy with 5-fluorouracil, vinblastine, and doxorubicin were removed from the study. Twenty-six patients were treated with high-dose cyclophosphamide (120 mg per kg) and 16 of these patients relapsed, usually at sites of previous metastases. A median survival time of 15 months and an overall response rate of 69 percent indicates that a single cycle of high-dose cyclophosphamide does not provide a significant benefit. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1989
44. Prostate cancer: a review emphasizing management options
- Author
-
Ellis, Georgiana K. and Livingston, Robert B.
- Subjects
Cancer -- Care and treatment ,Prostate cancer -- Care and treatment - Published
- 1988
45. Ford Bronco the spirited performance of the early '70s is back, this time without sacrificing fuel economy
- Author
-
Livingston, Robert
- Subjects
Automobiles -- Evaluation ,Automobiles ,Home and garden ,Travel, recreation and leisure ,Ford Bronco (Sport-utility vehicle) -- Evaluation - Published
- 1987
46. An evaluation of the Florida Bar.
- Author
-
Livingston, Robert E., McGinnis, Harold K., and Holmes, Keith A.
- Subjects
The Florida Bar -- Evaluation ,Clients' funds -- Management - Published
- 1986
47. Closing in on real estate law.
- Author
-
Livingston, Robert E.
- Subjects
Attorneys -- Specialties and specialists ,Real estate industry -- Methods - Published
- 1985
48. Improving performance of multigene panels for genomic analysis of cancer predisposition
- Author
-
Shirts, Brian H., Casadei, Silvia, Jacobson, Angela L., Lee, Ming K., Gulsuner, Suleyman, Bennett, Robin L., Miller, Margaret, Hall, Sarah A., Hampel, Heather, Hisama, Fuki M., Naylor, Lorraine V., Goetsch, Cathleen, Leppig, Kathleen, Tait, Jonathan F., Scroggins, Sheena M., Turner, Emily H., Livingston, Robert, Salipante, Stephen J., King, Mary-Claire, Walsh, Tom, and Pritchard, Colin C.
- Abstract
Purpose:Screening multiple genes for inherited cancer predisposition expands opportunities for cancer prevention; however, reports of variants of uncertain significance (VUS) may limit clinical usefulness. We used an expert-driven approach, exploiting all available information, to evaluate multigene panels for inherited cancer predisposition in a clinical series that included multiple cancer types and complex family histories.Methods:For 1,462 sequential patients referred for testing by BROCA or ColoSeq multigene panels, genomic DNA was sequenced and variants were interpreted by multiple experts using International Agency for Research on Cancer guidelines and incorporating evolutionary conservation, known and predicted variant consequences, and personal and family cancer history. Diagnostic yield was evaluated for various presenting conditions and family-history profiles.Results:Of 1,462 patients, 12% carried damaging mutations in established cancer genes. Diagnostic yield varied by clinical presentation. Actionable results were identified for 13% of breast and colorectal cancer patients and for 4% of cancer-free subjects, based on their family histories of cancer. Incidental findings explaining cancer in neither the patient nor the family were present in 1.7% of subjects. Less than 1% of patients carried VUS in BRCA1 or BRCA2. For all genes combined, initial reports contained VUS for 10.5% of patients, which declined to 7.5% of patients after reclassification based on additional information.Conclusions:Individualized interpretation of gene panels is a complex medical activity. Interpretation by multiple experts in the context of personal and family histories maximizes actionable results and minimizes reports of VUS.Genet Med 18 10, 974–981.
- Published
- 2016
- Full Text
- View/download PDF
49. Subsidized solidarity
- Author
-
Livingston, Robert Gerald
- Subjects
Business, general - Abstract
ROBERT GERALD LIVINGSTON, a visiting fellow at the German Historical Institute in Washington, D.C., points out an aspect of Germany's economy that EAMONN FINGLETON misses in his feature ('Germany's Economic [...]
- Published
- 2010
50. Inspired by Viewfinder column
- Author
-
Livingston, Robert
- Subjects
Consumer news and advice ,Electronics - Abstract
Mr. York--Wow! That article you wrote for the September issue sounded very 'inspired.' I always read what you have to say before delving into the magazine. I've seen some times [...]
- Published
- 2009
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