Literature DB >> 16710034

Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study.

Jeffrey S Dome1, Cecilia A Cotton, Elizabeth J Perlman, Norman E Breslow, John A Kalapurakal, Michael L Ritchey, Paul E Grundy, Marcio Malogolowkin, J Bruce Beckwith, Robert C Shamberger, Gerald M Haase, Max J Coppes, Peter Coccia, Morris Kletzel, Robert M Weetman, Milton Donaldson, Roger M Macklis, Daniel M Green.   

Abstract

PURPOSE: An objective of the fifth National Wilms' Tumor Study (NWTS-5) was to evaluate the efficacy of treatment regimens for anaplastic histology Wilms' tumor (AH). PATIENTS AND METHODS: Prospective single-arm studies were conducted. Patients with stage I AH were treated with vincristine and dactinomycin for 18 weeks. Patients with stages II to IV diffuse AH were treated with vincristine, doxorubicin, cyclophosphamide, and etoposide for 24 weeks plus flank/abdominal radiation.
RESULTS: A total of 2,596 patients with Wilms' tumor were enrolled onto NWTS-5, of whom 281 (10.8%) had AH. Four-year event-free survival (EFS) and overall survival (OS) estimates for assessable patients with stage I AH (n = 29) were 69.5% (95% CI, 46.9 to 84.0) and 82.6% (95% CI, 63.1 to 92.4). In comparison, 4-year EFS and OS estimates for patients with stage I favorable histology (FH; n = 473) were 92.4% (95% CI, 89.5 to 94.5) and 98.3% (95% CI, 96.4 to 99.2). Four-year EFS estimates for patients who underwent immediate nephrectomy with stages II (n = 23), III (n = 43), and IV (n = 15) diffuse AH were 82.6% (95% CI, 60.1 to 93.1), 64.7% (95% CI, 48.3 to 77.7), and 33.3% (95% CI, 12.2 to 56.4), respectively. OS was similar to EFS for these groups. There were no local recurrences among patients with stage II AH. Four-year EFS and OS estimates for patients with bilateral AH (n = 29) were 43.8% (95% CI, 24.2 to 61.8) and 55.2% (95% CI, 34.8 to 71.7), respectively.
CONCLUSION: The prognosis for patients with stage I AH is worse than that for patients with stage I FH. Novel treatment strategies are needed to improve outcomes for patients with AH, especially those with stage III to V disease.

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Year:  2006        PMID: 16710034     DOI: 10.1200/JCO.2005.04.7852

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  70 in total

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Authors:  Conrad V Fernandez; Ning Li; Elizabeth A Mullen; Paul E Grundy; Elizabeth J Perman; Robert C Shamberger; Peter F Ehrlich; Jeffrey S Dome
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Review 2.  Current management of wilms' tumor.

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4.  A Murine Model of K-RAS and β-Catenin Induced Renal Tumors Expresses High Levels of E2F1 and Resembles Human Wilms Tumor.

Authors:  Yajun Yi; Dina Polosukhina; Harold D Love; Austin Hembd; Michael Pickup; Harold L Moses; Harold N Lovvorn; Roy Zent; Peter E Clark
Journal:  J Urol       Date:  2015-04-29       Impact factor: 7.450

Review 5.  Management of bilateral Wilms tumours.

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6.  Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor.

Authors:  Peter F Ehrlich; James R Anderson; Michael L Ritchey; Jeffrey S Dome; Daniel M Green; Paul E Grundy; Elizabeth J Perlman; John A Kalapurakal; Norman E Breslow; Robert C Shamberger
Journal:  J Clin Oncol       Date:  2013-02-04       Impact factor: 44.544

Review 7.  Children's Oncology Group's 2013 blueprint for research: renal tumors.

Authors:  Jeffrey S Dome; Conrad V Fernandez; Elizabeth A Mullen; John A Kalapurakal; James I Geller; Vicki Huff; Eric J Gratias; David B Dix; Peter F Ehrlich; Geetika Khanna; Marcio H Malogolowkin; James R Anderson; Arlene Naranjo; Elizabeth J Perlman
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8.  Renal function after ifosfamide, carboplatin and etoposide (ICE) chemotherapy, nephrectomy and radiotherapy in children with Wilms tumour.

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9.  Prevalence and clinical impact of anaplasia in childhood rhabdomyosarcoma : a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.

Authors:  Stephen Qualman; James Lynch; Julia Bridge; David Parham; Lisa Teot; William Meyer; Alberto Pappo
Journal:  Cancer       Date:  2008-12-01       Impact factor: 6.860

Review 10.  Current and emerging chemotherapy treatment strategies for Wilms tumor in North America.

Authors:  Eric J Gratias; Jeffrey S Dome
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