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Outcome and Prognostic Factors in Stage III Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group Study AREN0532.
- Source :
-
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2018 Jan 20; Vol. 36 (3), pp. 254-261. Date of Electronic Publication: 2017 Dec 06. - Publication Year :
- 2018
-
Abstract
- Background The National Wilms Tumor Study (NWTS) approach to treating stage III favorable-histology Wilms tumor (FHWT) is Regimen DD4A (vincristine, dactinomycin, and doxorubicin) and radiation therapy. Further risk stratification is required to improve outcomes and reduce late effects. We evaluated clinical and biologic variables for patients with stage III FHWT without combined loss of heterozygosity (LOH) at chromosomes 1p and 16q treated in the Children's Oncology Group protocol AREN0532. Methods From October 2006 to August 2013, 588 prospectively treated, centrally reviewed patients with stage III FHWT were treated with Regimen DD4A and radiation therapy. Tumor LOH at 1p and 16q was determined by microsatellite analysis. Ineligible patients (n = 5) and those with combined LOH 1p/16q (n = 40) were excluded. Results A total of 535 patients with stage III disease were studied. Median follow-up was 5.2 years (range, 0.2 to 9.5). Four-year event-free survival (EFS) and overall survival estimates were 88% (95% CI, 85% to 91%) and 97% (95% CI, 95% to 99%), respectively. A total of 58 of 66 relapses occurred in the first 2 years, predominantly pulmonary (n = 36). Eighteen patients died, 14 secondary to disease. A better EFS was associated with negative lymph node status ( P < .01) and absence of LOH 1p or 16q ( P < .01), but not with gross residual disease or peritoneal implants. In contrast, the 4-year EFS was only 74% in patients with combined positive lymph node status and LOH 1p or 16q. A total of 123 patients (23%) had delayed nephrectomy. Submitted delayed nephrectomy histology showed anaplasia (n = 8; excluded from survival analysis); low risk/completely necrotic (n = 7; zero relapses), intermediate risk (n = 63; six relapses), and high-risk/blastemal type (n=7; five relapses). Conclusion Most patients with stage III FHWT had good EFS/overall survival with DD4A and radiation therapy. Combined lymph node and LOH status was highly predictive of EFS and should be considered as a potential prognostic marker for future trials.
- Subjects :
- Adolescent
Antineoplastic Combined Chemotherapy Protocols adverse effects
Biomarkers, Tumor genetics
Child
Child, Preschool
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 16
Dactinomycin administration & dosage
Doxorubicin administration & dosage
Female
Genetic Predisposition to Disease
Humans
Infant
Kidney Neoplasms genetics
Kidney Neoplasms mortality
Kidney Neoplasms pathology
Loss of Heterozygosity
Lymph Nodes pathology
Lymphatic Metastasis
Male
Neoplasm Staging
Nephrectomy
Phenotype
Progression-Free Survival
Prospective Studies
Radiation Dosage
Risk Factors
Time Factors
Vincristine administration & dosage
Wilms Tumor genetics
Wilms Tumor mortality
Wilms Tumor secondary
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Chemoradiotherapy, Adjuvant adverse effects
Kidney Neoplasms therapy
Wilms Tumor therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1527-7755
- Volume :
- 36
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 29211618
- Full Text :
- https://doi.org/10.1200/JCO.2017.73.7999