Literature DB >> 23174227

Loss of heterozygosity analysis at different chromosome regions in Wilms tumor confirms 1p allelic loss as a marker of worse prognosis: a study from the Italian Association of Pediatric Hematology and Oncology.

Filippo Spreafico1, Beatrice Gamba, Luigi Mariani, Paola Collini, Paolo D'Angelo, Andrea Pession, Andrea Di Cataldo, Paolo Indolfi, Marilina Nantron, Monica Terenziani, Carlo Morosi, Paolo Radice, Daniela Perotti.   

Abstract

PURPOSE: The specific aims of the AIEOP-TW-2003 protocol included prospectively investigating a possible association of tumor loss of heterozygosity with outcomes in children treated for Wilms tumor.
MATERIALS AND METHODS: We analyzed 125 unilateral favorable histology Wilms tumors registered between 2003 and 2008 in the Italian cooperative protocol for microsatellite markers mapped to chromosomes 1p, 7p, 11q, 16q and 22q.
RESULTS: The 3-year disease-free survival and overall survival probabilities were 0.87 (95% CI 0.81-0.93) and 0.98 (95% CI 0.96-1.0), respectively. Loss of heterozygosity at 1p was significantly associated with a worse disease-free survival (probability 0.67 for patients with and 0.92 for those without 1p loss of heterozygosity, p = 0.0009), as confirmed also by multivariate analysis adjusting for tumor stage and patient age at diagnosis. There was no difference in disease-free survival probability among children with loss of heterozygosity in the other chromosomal regions tested. The worse outlook for children older than 2 years at diagnosis did not seem to be influenced by the loss of heterozygosity patterns considered.
CONCLUSIONS: Chromosome 1p loss of heterozygosity seems to be a risk factor for nonanaplastic Wilms tumor, possibly regardless of other clinical factors. Our findings were uninformative regarding loss of heterozygosity in the other chromosomal regions tested.
Copyright © 2013 American Urological Association Education and Research, Inc. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23174227     DOI: 10.1016/j.juro.2012.09.009

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  14 in total

1.  Association of Chromosome 1q Gain With Inferior Survival in Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group.

Authors:  Eric J Gratias; Jeffrey S Dome; Lawrence J Jennings; Yueh-Yun Chi; Jing Tian; James Anderson; Paul Grundy; Elizabeth A Mullen; James I Geller; Conrad V Fernandez; Elizabeth J Perlman
Journal:  J Clin Oncol       Date:  2016-07-11       Impact factor: 44.544

Review 2.  Advances in Wilms Tumor Treatment and Biology: Progress Through International Collaboration.

Authors:  Jeffrey S Dome; Norbert Graf; James I Geller; Conrad V Fernandez; Elizabeth A Mullen; Filippo Spreafico; Marry Van den Heuvel-Eibrink; Kathy Pritchard-Jones
Journal:  J Clin Oncol       Date:  2015-08-24       Impact factor: 44.544

Review 3.  Biomarkers for Wilms Tumor: A Systematic Review.

Authors:  Eugene B Cone; Stewart S Dalton; Megan Van Noord; Elizabeth T Tracy; Henry E Rice; Jonathan C Routh
Journal:  J Urol       Date:  2016-05-31       Impact factor: 7.450

Review 4.  Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review.

Authors:  Changkai Deng; Rong Dai; Xuliang Li; Feng Liu
Journal:  Cancer Sci       Date:  2016-03-18       Impact factor: 6.716

Review 5.  Cell-free circulating tumor DNA analysis for breast cancer and its clinical utilization as a biomarker.

Authors:  Ru Wang; Xiao Li; Huimin Zhang; Ke Wang; Jianjun He
Journal:  Oncotarget       Date:  2017-09-01

6.  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

7.  Combining miRNA and mRNA Expression Profiles in Wilms Tumor Subtypes.

Authors:  Nicole Ludwig; Tamara V Werner; Christina Backes; Patrick Trampert; Manfred Gessler; Andreas Keller; Hans-Peter Lenhof; Norbert Graf; Eckart Meese
Journal:  Int J Mol Sci       Date:  2016-03-30       Impact factor: 5.923

8.  Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences.

Authors:  Filippo Spreafico; Sara Ciceri; Beatrice Gamba; Federica Torri; Monica Terenziani; Paola Collini; Fabio Macciardi; Paolo Radice; Daniela Perotti
Journal:  Oncotarget       Date:  2016-02-23

9.  Loss of heterozygosity on chromosome 16q increases relapse risk in Wilms' tumor: a meta-analysis.

Authors:  Zhenyu Pan; Hairong He; Lina Tang; Qingting Bu; Hua Cheng; Anmin Wang; Jun Lyu; Haisheng You
Journal:  Oncotarget       Date:  2017-08-11

Review 10.  Biological Drivers of Wilms Tumor Prognosis and Treatment.

Authors:  Hannah M Phelps; Saara Kaviany; Scott C Borinstein; Harold N Lovvorn
Journal:  Children (Basel)       Date:  2018-10-26
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