Literature DB >> 20582946

Stromal and epithelial predominant Wilms tumours have an excellent outcome: the SIOP 93 01 experience.

Arnauld C Verschuur1, Gordan M Vujanic, Harm Van Tinteren, Kathy Pritchard Jones, Jan de Kraker, Bengt Sandstedt.   

Abstract

BACKGROUND: Wilms tumour (WT) has various subtypes that are correlated with prognosis and require distinct therapy. Stromal predominant (SpWT) and epithelial WT (EpWT) have previously been associated with a good outcome. The current analysis describes the outcome and (tumour) characteristics of all patients with SpWT, EpWT, including highly differentiated epithelial type (HDET), treated according to the International Society of Pediatric Oncology (SIOP) 93-01 study. PROCEDURE: All children older than 6 months and below 18 years of age with localized or metastatic WT and intermediate risk (IR) histology or HDET treated with pre-operative chemotherapy were included in the present analysis.
RESULTS: A total of 1,389 eligible patients had IR or HDET histology: 1% HDET, 4% EpWT, 10% SpWT, and 85% other IR. For EpWT/HDET, 93% had stage I/IIN-, 5-year EFS was 90.2% and overall survival of (OS) 98.4%, as compared to 84.0% and 92.5% in other IR histology (NS). Stage I EpWT/HDET had a significant better outcome than stage I of other IR. In SpWT 82% of cases had stage I/IIN-; 5-year EFS was 94.3% and OS 99.2%, significantly better compared to other IR histology. All patients with stage I are alive (2/149 relapses); 3/52 stage IIN-, 2/21 stage IIN+/III, and 6/12 stage IV patients relapsed (1 deceased per stage group).
CONCLUSIONS: The good outcome for EpWT and SpWT generally is very good which may be related to low age and low stage in most cases. A reduction of treatment intensity and/or duration may be justified especially for low stage SpWT that has an EFS close to 100%. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20582946     DOI: 10.1002/pbc.22496

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  12 in total

Review 1.  Position paper: Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol.

Authors:  Marry M van den Heuvel-Eibrink; Janna A Hol; Kathy Pritchard-Jones; Harm van Tinteren; Rhoikos Furtwängler; Arnauld C Verschuur; Gordan M Vujanic; Ivo Leuschner; Jesper Brok; Christian Rübe; Anne M Smets; Geert O Janssens; Jan Godzinski; Gema L Ramírez-Villar; Beatriz de Camargo; Heidi Segers; Paola Collini; Manfred Gessler; Christophe Bergeron; Filippo Spreafico; Norbert Graf
Journal:  Nat Rev Urol       Date:  2017-10-31       Impact factor: 14.432

2.  Angiogenin expression in human kidneys and Wilms' tumours: relationship with hypoxia and angiogenic factors.

Authors:  Pramila Ramani; Alison Headford; Emile Sowa-Avugrah; Linda P Hunt
Journal:  Int J Exp Pathol       Date:  2013-02-19       Impact factor: 1.925

3.  Deletions of 16q in Wilms tumors localize to blastemal-anaplastic cells and are associated with reduced expression of the IRXB renal tubulogenesis gene cluster.

Authors:  Linda Holmquist Mengelbier; Jenny Karlsson; David Lindgren; Ingrid Øra; Margareth Isaksson; Ildiko Frigyesi; Attila Frigyesi; Johannes Bras; Bengt Sandstedt; David Gisselsson
Journal:  Am J Pathol       Date:  2010-09-16       Impact factor: 4.307

4.  Outcomes based on histopathologic response to preoperative chemotherapy in children with bilateral Wilms tumor: A prospective study (COG AREN0534).

Authors:  Murali M Chintagumpala; Elizabeth J Perlman; Brett Tornwall; Yueh-Yun Chi; Yeonil Kim; Fredric A Hoffer; John A Kalapurakal; Anne B Warwick; Robert C Shamberger; Geetika Khanna; Thomas E Hamilton; Kenneth W Gow; Arnold C Paulino; Eric J Gratias; Elizabeth A Mullen; James I Geller; Conrad V Fernandez; Michael L Ritchey; Paul E Grundy; Jeffrey S Dome; Peter F Ehrlich
Journal:  Cancer       Date:  2022-04-05       Impact factor: 6.921

5.  Correlations between histological characterizations and methylation statuses of tumour suppressor genes in Wilms' tumours.

Authors:  Yen-Chein Lai; Meng-Yao Lu; Wen-Chung Wang; Tai-Cheng Hou; Chen-Yun Kuo
Journal:  Int J Exp Pathol       Date:  2022-04-18       Impact factor: 2.793

Review 6.  Oncology: the role of partial nephrectomy in Wilms tumor.

Authors:  Miriam Harel; John H Makari; Fernando A Ferrer
Journal:  Curr Urol Rep       Date:  2013-08       Impact factor: 3.092

7.  Outcome analysis of stage I epithelial-predominant favorable-histology Wilms tumors: A report from Children's Oncology Group study AREN03B2.

Authors:  Lauren N Parsons; Elizabeth A Mullen; James I Geller; Yueh-Yun Chi; Geetika Khanna; Richard D Glick; Jennifer H Aldrink; Kelly L Vallance; Yeonil Kim; Conrad V Fernandez; Jeffrey S Dome; Elizabeth J Perlman
Journal:  Cancer       Date:  2020-04-08       Impact factor: 6.860

8.  [Tumor size and prognosis in patients with Wilms tumor].

Authors:  Valentina Oliveira Provenzi; Rafael Fabiano Machado Rosa; Rosana Cardoso Manique Rosa; Adriana Vial Roehe; Pedro Paulo Albino dos Santos; Fabrízia Rennó Sodero Faulhaber; Ceres Andréia Vieira de Oliveira; Paulo Ricardo Gazzola Zen
Journal:  Rev Paul Pediatr       Date:  2015-01-23

9.  Expression of PAX2 and PAX8 in Wilms Tumor: A Tissue Microarray-based Immunohistochemical Study.

Authors:  Salma Sefidbakht; Atieh Khorsand; Sahar Omidi; Sedigheh Mohsenpourian; Elham Mirzaian
Journal:  Iran J Pathol       Date:  2021-05-09

10.  Composite tumor of metanephric adenoma and Wilms' tumor of the kidney: A case report and review of the literature.

Authors:  Pengcheng Zhu; Fei Yan; Zixuan Yang; Li Meng; Qilin Ao
Journal:  Oncol Lett       Date:  2013-01-22       Impact factor: 2.967

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