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3. Illustrations

Author

Travis, W. D., Colby, T. V., Corrin, B., Shimosato, Y., Brambilla, E., Travis, W. D., Colby, T. V., Corrin, B., Shimosato, Y., and Brambilla, E.

Published
1999
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9. Anatomical resections are superior to wedge resections for overall survival in patients with Stage 1 typical carcinoids

Author

Filosso, P. L., Guerrera, F., Falco, N. R., Thomas, P., Garcia Yuste, M., Rocco, G., Welter, S., Moreno Casado, P., Rendina, E. A., Venuta, F., Ampollini, L., Nosotti, M., Raveglia, F., Rena, O., Stella, F., Larocca, V., Ardissone, F., Brunelli, A., Margaritora, S., Travis, W. D., Sagan, D., Sarkaria, I., Evangelista, A., Yuste, M. G., Lim, E., Papagiannopoulos, K., Asamura, H., Filosso, Pier Luigi, Guerrera, Francesco, Falco, Nicola Rosario, Thomas, Pascal, Garcia Yuste, Mariano, Rocco, Gaetano, Welter, Stefan, Moreno Casado, Paula, Rendina, Erino Angelo, Venuta, Federico, Ampollini, Luca, Nosotti, Mario, Raveglia, Federico, Rena, Ottavio, Stella, Franco, Larocca, Valentina, Ardissone, Francesco, Brunelli, Alessandro, Margaritora, Stefano, Travis, William D, Sagan, Dariusz, Sarkaria, Inderpal, Evangelista, Andrea, Yuste, Mariano Garcia, Lim, Eric, Papagiannopoulos, Konstantino, and Asamura, Hisao

Subjects
Male, Pulmonary and Respiratory Medicine, medicine.medical_specialty, Lung Neoplasms, Thoracic, overall survival, Medizin, Carcinoid Tumor, 030204 cardiovascular system & hematology, lung neoplasms, surgery, 03 medical and health sciences, 0302 clinical medicine, male, Interquartile range, Settore MED/21 - CHIRURGIA TORACICA, middle aged, Medicine, Humans, Cumulative incidence, carcinoid tumor, Stage (cooking), Pneumonectomy, humans, Lung, pneumonectomy, Aged, Retrospective Studies, business.industry, Proportional hazards model, Hazard ratio, Retrospective cohort study, General Medicine, Middle Aged, Surgery, aged, retrospective studies, typical carcinoid, female, 030228 respiratory system, Propensity score matching, Female, business, Cardiology and Cardiovascular Medicine, neoplasm, Wedge resection (lung)
Abstract

OBJECTIVES Typical carcinoids (TCs) are rare, slow-growing neoplasms, usually characterized by satisfactory surgical outcomes. Due to the rarity of TCs, international guidelines for the management of particular clinical presentations currently do not exist. In particular, non-anatomical resections (wedges) are sometimes advocated for Stage 1 TCs because of their indolent behaviour. The aim of this paper was to evaluate the most effective type of surgery for Stage 1 TCs, using the European Society of Thoracic Surgeons retrospective database of the Neuroendocrine Tumors of the Lung Working Group. METHODS We analysed the effect of surgical procedure on the survival of patients with Stage 1 TCs. Overall survival (OS) was calculated from the date of intervention. The cumulative incidence of cause-specific death (tumour- and non-tumour-related) was also estimated. The impact of the surgical procedure (i.e. lobectomy vs segmentectomy vs wedge resection) on survival was investigated using the Cox model with shared frailty (for OS, accounting for the within-centre correlation) and the Fine and Gray model (for cause-specific mortality) using the approach based on the multinomial propensity score. Effects were estimated including in the model the logit-transformed propensity scores of segmentectomy and wedge resection as covariates. RESULTS A total of 876 patients with Stage 1 TCs (569 women, 65%) were included in this study. The median age was 60 years (interquartile range 47–69). At the last follow-up, 66 patients had died: The 5-year OS rate was 94.3% [95% confidence interval (CI) 92.2–95.9]. The 5-year cumulative incidences of tumour- and non-tumour-related deaths were 2.4% (95% CI 1.4–3.9) and 3.9% (95% CI 2.5–5.6%), respectively. The analysis performed using the multinomial propensity score approach confirmed the significantly worse survival of patients treated with a wedge resection compared to those treated with a lobectomy (hazard ratio 2.01, 95% CI 1.09–3.69; P = 0.024). Similar effects of wedge resection are detectable for cause-specific deaths: tumour-related (hazard ratio 2.28, 95% CI 0.86–6.02; P = 0.096) and non-tumour-related (hazard ratio 1.74, 95% CI 0.89–3.40; P = 0.105). CONCLUSIONS In a large cohort of patients, we were able to demonstrate the superiority of anatomical surgical resection in Stage 1 TCs in terms of OS. This result should therefore be considered for future clinical guidelines for the management of TCs.

Published
2019

18. Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper

Author

Lynch, D. A., Sverzellati, N., Travis, W. D., Brown, K. K., Colby, T. V., Galvin, J. R., Goldin, J. G., Hansell, D. M., Inoue, Y., Johkoh, T., Nicholson, A. G., Knight, S. L., Raoof, S., Richeldi, Luca, Ryerson, C. J., Ryu, J. H., Wells, A. U., Richeldi L. (ORCID:0000-0001-8594-1448), Lynch, D. A., Sverzellati, N., Travis, W. D., Brown, K. K., Colby, T. V., Galvin, J. R., Goldin, J. G., Hansell, D. M., Inoue, Y., Johkoh, T., Nicholson, A. G., Knight, S. L., Raoof, S., Richeldi, Luca, Ryerson, C. J., Ryu, J. H., Wells, A. U., and Richeldi L. (ORCID:0000-0001-8594-1448)

Abstract

This Review provides an updated approach to the diagnosis of idiopathic pulmonary fibrosis (IPF), based on a systematic search of the medical literature and the expert opinion of members of the Fleischner Society. A checklist is provided for the clinical evaluation of patients with suspected usual interstitial pneumonia (UIP). The role of CT is expanded to permit diagnosis of IPF without surgical lung biopsy in select cases when CT shows a probable UIP pattern. Additional investigations, including surgical lung biopsy, should be considered in patients with either clinical or CT findings that are indeterminate for IPF. A multidisciplinary approach is particularly important when deciding to perform additional diagnostic assessments, integrating biopsy results with clinical and CT features, and establishing a working diagnosis of IPF if lung tissue is not available. A working diagnosis of IPF should be reviewed at regular intervals since the diagnosis might change. Criteria are presented to establish confident and working diagnoses of IPF.

Published
2018

19. Diagnosis of idiopathic pulmonary fibrosis An Official ATS/ERS/JRS/ALAT Clinical practice guideline

Author

Raghu, G., Remy-Jardin, M., Myers, J. L., Richeldi, Luca, Ryerson, C. J., Lederer, D. J., Behr, J., Cottin, V., Danoff, S. K., Morell, F., Flaherty, K. R., Wells, A., Martinez, F. J., Azuma, A., Bice, T. J., Bouros, D., Brown, K. K., Collard, H. R., Duggal, A., Galvin, L., Inoue, Y., Gisli Jenkins, R., Johkoh, T., Kazerooni, E. A., Kitaichi, M., Knight, S. L., Mansour, G., Nicholson, A. G., Pipavath, S. N. J., Buendia-Roldan, I., Selman, M., Travis, W. D., Walsh, S., Wilson, K. C., Richeldi L. (ORCID:0000-0001-8594-1448), Raghu, G., Remy-Jardin, M., Myers, J. L., Richeldi, Luca, Ryerson, C. J., Lederer, D. J., Behr, J., Cottin, V., Danoff, S. K., Morell, F., Flaherty, K. R., Wells, A., Martinez, F. J., Azuma, A., Bice, T. J., Bouros, D., Brown, K. K., Collard, H. R., Duggal, A., Galvin, L., Inoue, Y., Gisli Jenkins, R., Johkoh, T., Kazerooni, E. A., Kitaichi, M., Knight, S. L., Mansour, G., Nicholson, A. G., Pipavath, S. N. J., Buendia-Roldan, I., Selman, M., Travis, W. D., Walsh, S., Wilson, K. C., and Richeldi L. (ORCID:0000-0001-8594-1448)

Abstract

Background: This document provides clinical recommendations for the diagnosis of idiopathic pulmonary fibrosis (IPF). It represents a collaborative effort between the American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Society. Methods: The evidence syntheses were discussed and recommendations formulated by a multidisciplinary committee of IPF experts. The evidence was appraised and recommendations were formulated, written, and graded using the Grading of Recommendations, Assessment, Development, and Evaluation approach. Results: The guideline panel updated the diagnostic criteria for IPF Previously defined patterns of usual interstitial pneumonia (UIP) were refined to patterns of UIP, probable UIP, indeterminate, and alternate diagnosis. For patients with newly detected interstitial lung disease (ILD) who have a high-resolution computed tomography scan pattern of probable UIP, indeterminate, or an alternative diagnosis, conditional recommendations were made for performing BAL and surgical lung biopsy; because of lack of evidence, no recommendation was made for or against performing transbronchial lung biopsy or lung cryobiopsy. In contrast, for patients with newly detected ILD who have a high-resolution computed tomography scan pattern of UIP, strong recommendations were made against performing surgical lung biopsy, transbronchial lung biopsy, and lung cryobiopsy, and a conditional recommendation was made against performing BAL. Additional recommendations included a conditional recommendation for multidisciplinary discussion and a strong recommendation against measurement of serum biomarkers for the sole purpose of distinguishing IPF from other ILDs. Conclusions: The guideline panel provided recommendations related to the diagnosis of IPF.

Published
2018

20. Pulmonary neuroendocrine (carcinoid) tumors: European Neuroendocrine Tumor Society expert consensus and recommendations for best practice for typical and atypical pulmonary carcinoids

Author

Caplin, M. E., Baudin, E., Ferolla, P., Filosso, P., Garcia-Yuste, M., Lim, E., Oberg, K., Pelosi, G., Perren, A., Rossi, R. E., Travis, W. D., Bartsch, Detlief, Capdevila, Jaume, Costa, Frederico, Cwikla, Jaroslaw, de Herder, Wouter, Delle Fave, Gianfranco, Eriksson, Barbro, Falconi, Massimo, Ferone, Diego, Gross, David, Grossman, Ashley, Ito, Tetsuhide, Jensen, Robert, Kaltsas, Gregory, Kelestimur, Fahrettin, Kianmanesh, Reza, Knigge, Ulrich, Kos-Kudla, Beata, Krenning, Eric, Mitry, Emmanuel, Nicolson, Marianne, O'Connor, Juan, O'Toole, Dermot, Pape, Ulrich-Frank, Pavel, Marianne, Ramage, John, Raymond, Eric, Rindi, Guido, Rockall, Andrea, Ruszniewski, Philippe, Salazar, Ramon, Scarpa, Aldo, Sedlackova, Eva, Sundin, Anders, Toumpanakis, Christos, Vullierme, Marie-Pierre, Weber, Wolfgang, Wiedenmann, Bertram, and Zheng-Pei, Zeng

Abstract

This is an expert consensus from the European Neuroendocrine Tumor Society recommending best practice for the management of pulmonary neuroendocrine tumors including typical and atypical carcinoids. It emphasizes the latest discussion on nomenclature, advances and utility of new diagnostic techniques as well as the limited evidence and difficulties in determining the optimal therapeutic strategy

Published
2017

21. Lung Cancer Screening: Clinical Practice Guidelines in Oncology

Author

Wood, D. E., Eapen, G. A., Ettinger, D. S., Hou, L., Jackman, D., Kazerooni, E., Klippenstein, D., Lackner, R. P., Leard, L., Leung, A. N. C., Massion, P. P., Meyers, B. F., Munden, R. F., Otterson, G. A., Peairs, K., Pipavath, S., Pratt-Pozo, C., Reddy, C., Reid, M. E., Rotter, A. J., Matthew Schabath, Sequist, L. V., Tong, B. C., Travis, W. D., Unger, M., and Yang, S. C.

Subjects
Lung Neoplasms, Humans, Article, Early Detection of Cancer
Published
2012

23. An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias

Author

Travis, W. D., Costabel, U., Hansell, D. M., King, Jr. T. E., Lynch, D. A., Nicholson, A. G., Ryerson, C. J., Ryu, J. H., Selman, M., Wells, A. U., Behr, J., Bouros, D., Brown, K. K., Colby, T. V., Collard, H. R., Cordeiro, C. R., Cottin, V., Crestani, B., Drent, M., Dudden, R. F., Egan, J., Flaherty, K., Hogaboam, C., Inoue, Y., Johkoh, T., Kim, D. S., Kitaichi, M., Loyd, J., Martinez, F. J., Myers, J., Protzko, S., Raghu, G., Richeldi, Luca, Sverzellati, N., Swigris, J., Valeyre, D., Richeldi L. (ORCID:0000-0001-8594-1448), Travis, W. D., Costabel, U., Hansell, D. M., King, Jr. T. E., Lynch, D. A., Nicholson, A. G., Ryerson, C. J., Ryu, J. H., Selman, M., Wells, A. U., Behr, J., Bouros, D., Brown, K. K., Colby, T. V., Collard, H. R., Cordeiro, C. R., Cottin, V., Crestani, B., Drent, M., Dudden, R. F., Egan, J., Flaherty, K., Hogaboam, C., Inoue, Y., Johkoh, T., Kim, D. S., Kitaichi, M., Loyd, J., Martinez, F. J., Myers, J., Protzko, S., Raghu, G., Richeldi, Luca, Sverzellati, N., Swigris, J., Valeyre, D., and Richeldi L. (ORCID:0000-0001-8594-1448)

Abstract

Background: In 2002 the American Thoracic Society/European Respiratory Society (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs)definedseven specific entities, andprovided standardized terminology anddiagnosticcriteria. Inaddition, thehistorical "gold standard" of histologic diagnosiswas replaced by amultidisciplinary approach. Since 2002 many publications have provided newinformation about IIPs. Purpose: The objective of this statement is to update the 2002 ATS/ ERS classification of IIPs. Methods: An international multidisciplinary panel was formed and developed key questions that were addressed through a review of the literature published between 2000 and 2011. Results: Substantial progress has been made in IIPs since the previous classification. Nonspecific interstitial pneumonia is now better defined. Respiratory bronchiolitis-interstitial lung disease is now commonly diagnosed without surgical biopsy. The clinical course of idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia is recognized to be heterogeneous. Acute exacerbation of IIPs is now well defined. A substantial percentage of patients with IIP are difficult to classify, often due to mixed patterns of lung injury. A classification based on observed disease behavior is proposed for patients who are difficult to classify or for entities with heterogeneity in clinical course. A group of rare entities, including pleuroparenchymal fibroelastosis and rare histologic patterns, is introduced. The rapidly evolving field of molecular markers is reviewed with the intent of promoting additional investigations that may help in determining diagnosis, and potentially prognosis and treatment. Conclusions: This update is a supplement to the previous 2002 IIP classification document. It outlines advances in the past decade and potential areas for future investigation. Copyright © 2013 by the American Thoracic Society.

Published
2013

24. American thoracic society/European respiratory society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias

Author

Travis, W. D., King, J. r. T. E., Bateman, E. D., Lynch, D. A., Capron, F., Colby, T. V., Cordier, J. F., Dubois, R. M., Hunninghake, G. W., Kitaichi, M., Müller, N. L., Myers, J. L., Nagai, S., Nicholson, A., Raghu, G., Wallaert, B., Brambilla, C. G., Brown, K. K., Cherniaev, A. L., Costabel, U., Coultas, D. B., Davis, G. S., Demedts, M. G., Douglas, W. W., Egan, J., Eklund, A. G., Fabbri, L. M., Henke, C. A., Hubbard, R. B., Inoue, Y., Izumi, T., Jansen, H. M., Johnston, I., Kim, D. S., Khalil, N., Lake, F. R., Lungarella, Giuseppe, Lynch III, J. P., Mapel, D. W., Martinez, F., Matthay, R., Newman, L. S., Noble, P. W., Ohta, K., Olivieri, D., Ortiz, L. A., Poletti, V., and Rodriguez Roisin, R.

Published
2002

27. The Diesel Exhaust in Miners Study: A Nested Case-Control Study of Lung Cancer and Diesel Exhaust

Author

Silverman, D. T., primary, Samanic, C. M., additional, Lubin, J. H., additional, Blair, A. E., additional, Stewart, P. A., additional, Vermeulen, R., additional, Coble, J. B., additional, Rothman, N., additional, Schleiff, P. L., additional, Travis, W. D., additional, Ziegler, R. G., additional, Wacholder, S., additional, and Attfield, M. D., additional

Published
2012
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28. International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society: International Multidisciplinary Classification of Lung Adenocarcinoma: Executive Summary

Author

Travis, W. D., primary, Brambilla, E., additional, Noguchi, M., additional, Nicholson, A. G., additional, Geisinger, K., additional, Yatabe, Y., additional, Powell, C. A., additional, Beer, D., additional, Riely, G., additional, Garg, K., additional, Austin, J. H. M., additional, Rusch, V. W., additional, Hirsch, F. R., additional, Jett, J., additional, Yang, P.-C., additional, and Gould, M., additional

Published
2011
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34. Resident Cellular Components of the Human Lung: Current Knowledge and Goals for Research on Cell Phenotyping and Function

Author

Franks, T. J., primary, Colby, T. V., additional, Travis, W. D., additional, Tuder, R. M., additional, Reynolds, H. Y., additional, Brody, A. R., additional, Cardoso, W. V., additional, Crystal, R. G., additional, Drake, C. J., additional, Engelhardt, J., additional, Frid, M., additional, Herzog, E., additional, Mason, R., additional, Phan, S. H., additional, Randell, S. H., additional, Rose, M. C., additional, Stevens, T., additional, Serge, J., additional, Sunday, M. E., additional, Voynow, J. A., additional, Weinstein, B. M., additional, Whitsett, J., additional, and Williams, M. C., additional

Published
2008
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37. hTR repressor-related gene on human chromosome 10p15.1

Author

Miura, N, primary, Onuki, N, additional, Rathi, A, additional, Virmani, A, additional, Nakamoto, S, additional, Kishimoto, Y, additional, Murawaki, Y, additional, Kawasaki, H, additional, Hasegawa, J, additional, Oshimura, M, additional, Travis, W D, additional, and Gazdar, A F, additional

Published
2001
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38. Response

Author

TRAVIS, L. B., primary, CURTIS, R. E., additional, BENNETT, W. P., additional, HANKEY, B. F., additional, BOICE, J. D., additional, and TRAVIS, W. D., additional

Published
1996
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41. Clinical, pathologic, and biochemical features of a cholesterol lipidosis accompanied by hyperlipidemia and xanthomas

Author

Filling-Katz, M. R., primary, Miller, S.P.F., additional, Merrick, H. F., additional, Travis, W. D., additional, Gregg, R. E., additional, Tsokos, M., additional, Comly, M., additional, Kaneski, C. R., additional, Mackie, S., additional, Lebovics, R. S., additional, Blanchette-Mackie, E. J., additional, Brady, R. O., additional, and Pentchev, P. G., additional

Published
1992
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50. Pulmonary pathology of Erdheim-Chester disease.

Author

Rush, Walter L., Andriko, Jo Ann W., Galateau-Salle, Francoise, Brambilla, Elizabeth, Brambilla, Christian, I. Ziany-bey, Rosado-de-Christenson, Melissa L., Travis, William D., Rush, W L, Andriko, J A, Galateau-Salle, F, Brambilla, E, Brambilla, C, Ziany-bey, I, Rosado-de-Christenson, M L, and Travis, W D

Published
2000
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