Literature DB >> 32267967

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

Lauren N Parsons1, Elizabeth A Mullen2, James I Geller3, Yueh-Yun Chi4, Geetika Khanna5, Richard D Glick6, Jennifer H Aldrink7, Kelly L Vallance8, Yeonil Kim4, Conrad V Fernandez9,10, Jeffrey S Dome11, Elizabeth J Perlman12.   

Abstract

BACKGROUND: Stage I epithelial-predominant favorable-histology Wilms tumors (EFHWTs) have long been suspected to have an excellent outcome. This study investigates the clinical and pathologic features of patients with stage I EFHWTs to better evaluate the potential for a reduction of chemotherapy and its associated toxicity.
METHODS: All patients registered in the Children's Oncology Group (COG) AREN03B2 study between 2006 and 2017 with stage I EFHWTs were identified. EFHWTs were defined as tumors with at least 66% epithelial differentiation, regardless of the degree of differentiation. Clinical information was abstracted from COG records. Event-free survival (EFS) and overall survival (OS) were calculated and compared between groups based on age and therapy.
RESULTS: The 4-year EFS rate was 96.2% (95% confidence interval, 92%-100%), and the OS rate was 100%; EFS and OS did not statistically significantly differ with the age at diagnosis (<48 vs ≥48 months; P = .37) or treatment (EE4A vs observation only; P = .55). Six events were reported. Three patients developed contralateral tumors and did not otherwise relapse; none of these had nephrogenic rests or a recognized predisposition syndrome. Three patients developed metastatic recurrence; all 3 had received EE4A as their primary therapy after nephrectomy.
CONCLUSIONS: These findings demonstrate an excellent outcome for stage I EFHWTs with >95% EFS and OS. These data support the utility of investigating the treatment of stage I EFHWTs with observation alone after nephrectomy.
© 2020 American Cancer Society.

Entities:  

Keywords:  Wilms tumor; epithelial predominant; nephroblastoma

Mesh:

Year:  2020        PMID: 32267967      PMCID: PMC7717680          DOI: 10.1002/cncr.32855

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  20 in total

1.  BRAF mutations in metanephric adenoma of the kidney.

Authors:  Toni K Choueiri; John Cheville; Emanuele Palescandolo; André P Fay; Philip W Kantoff; Michael B Atkins; Jesse K McKenney; Victoria Brown; Megan E Lampron; Ming Zhou; Michelle S Hirsch; Sabina Signoretti
Journal:  Eur Urol       Date:  2012-06-09       Impact factor: 20.096

2.  Improved survival with lymph node sampling in Wilms tumor.

Authors:  Ying Zhuge; Michael C Cheung; Relin Yang; Leonidas G Koniaris; Holly L Neville; Juan E Sola
Journal:  J Surg Res       Date:  2011-01-14       Impact factor: 2.192

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

Authors:  Arnauld C Verschuur; Gordan M Vujanic; Harm Van Tinteren; Kathy Pritchard Jones; Jan de Kraker; Bengt Sandstedt
Journal:  Pediatr Blood Cancer       Date:  2010-08       Impact factor: 3.167

4.  Twenty-five year follow-up of childhood Wilms tumor: a report from the Childhood Cancer Survivor Study.

Authors:  Amanda M Termuhlen; Jean M Tersak; Qi Liu; Yutaka Yasui; Marilyn Stovall; Rita Weathers; Melvin Deutsch; Charles A Sklar; Kevin C Oeffinger; Greg Armstrong; Leslie L Robison; Daniel M Green
Journal:  Pediatr Blood Cancer       Date:  2011-03-07       Impact factor: 3.167

5.  Lymph node involvement in Wilms tumor: results from National Wilms Tumor Studies 4 and 5.

Authors:  Kathleen Kieran; James R Anderson; Jeffrey S Dome; Peter F Ehrlich; Michael L Ritchey; Robert C Shamberger; Elizabeth J Perlman; Daniel M Green; Andrew M Davidoff
Journal:  J Pediatr Surg       Date:  2012-04       Impact factor: 2.545

6.  Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic Wilms Tumor.

Authors:  H Reinhard; O Semler; D Bürger; U Bode; M Flentje; U Göbel; P Gutjahr; I Leuschner; E Maass; F Niggli; H G Scheel-Walter; M Stöckle; J W Thüroff; J Tröger; A Weirich; D von Schweinitz; A Zoubek; N Graf
Journal:  Klin Padiatr       Date:  2004 May-Jun       Impact factor: 1.349

7.  Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study.

Authors:  Samantha Gadd; Vicki Huff; Chiang-Ching Huang; E Cristy Ruteshouser; Jeffrey S Dome; Paul E Grundy; Norman Breslow; Lawrence Jennings; Daniel M Green; J Bruce Beckwith; Elizabeth J Perlman
Journal:  Neoplasia       Date:  2012-08       Impact factor: 5.715

8.  A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.

Authors:  Amy E Armstrong; Samantha Gadd; Vicki Huff; Daniela S Gerhard; Jeffrey S Dome; Elizabeth J Perlman
Journal:  PLoS One       Date:  2018-12-13       Impact factor: 3.240

9.  Prognostic significance of age in 5631 patients with Wilms tumour prospectively registered in International Society of Paediatric Oncology (SIOP) 93-01 and 2001.

Authors:  J A Hol; M I Lopez-Yurda; H Van Tinteren; M Van Grotel; J Godzinski; G Vujanic; F Oldenburger; B De Camargo; G L Ramírez-Villar; C Bergeron; K Pritchard-Jones; N Graf; M M Van den Heuvel-Eibrink
Journal:  PLoS One       Date:  2019-08-19       Impact factor: 3.240

10.  Distinct clinicopathological features in metanephric adenoma harboring BRAF mutation.

Authors:  Anna Caliò; John N Eble; Ondrej Hes; Guido Martignoni; Saul E Harari; Sean R Williamson; Matteo Brunelli; Adeboye O Osunkoya; Lisha Wang; Eva Comperat; Antonio Lopez-Beltran; Mingsheng Wang; Shaobo Zhang; Kendra L Curless; Kristin M Post; Hsim-Yee Chang; Claudio Luchini; Lee Ann Baldrige; Gregory T MacLennan; Rodolfo Montironi; David J Grignon; Liang Cheng
Journal:  Oncotarget       Date:  2016-08-08
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  1 in total

Review 1.  TRIM28 variants and Wilms' tumour predisposition.

Authors:  Janna A Hol; Illja J Diets; Ronald R de Krijger; Marry M van den Heuvel-Eibrink; Marjolijn Cj Jongmans; Roland P Kuiper
Journal:  J Pathol       Date:  2021-03-15       Impact factor: 7.996

  1 in total

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