Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study

PURPOSE: Multidisciplinary management of Wilms tumor has been defined through multicenter prospective studies and an average expected patient cure rate of 90%. In sub-Saharan Africa, such studies are uncommon. After the encouraging results of the first Groupe Franco-Africain d'Oncologie Pédiatr...

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Main Authors: Atteby Jean-Jacques Yao, Claude Moreira, Fousseyni Traoré, Sonia Kaboret, Angele Pondy, Mbolanirina Lala Rakotomahefa Narison, Koffi M. Guedenon, Brenda Mallon, Catherine Patte
Format: Article
Language:English
Published: American Society of Clinical Oncology 2019-09-01
Series:Journal of Global Oncology
Online Access:http://ascopubs.org/doi/10.1200/JGO.18.00204
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spelling doaj-298cadb3726b486fb0c716aee2f1f6072020-11-25T03:20:11ZengAmerican Society of Clinical OncologyJournal of Global Oncology2378-95062019-09-0151810.1200/JGO.18.002041Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group StudyAtteby Jean-Jacques Yao0Claude Moreira1Fousseyni Traoré2Sonia Kaboret3Angele Pondy4Mbolanirina Lala Rakotomahefa Narison5Koffi M. Guedenon6Brenda Mallon7Catherine Patte8Hôpital de Treichville, Abidjan, Ivory CoastHôpital Aristide Le Dantec, Université Cheikh Anta Diop de Dakar, Dakar, SenegalHôpital Gabriel Touré, Bamako, MaliHopital Charles de Gaulle, Centre Hospitalier Universitaire Pédiatrique, Ouagadougou, Burkina FasoCentre Mère et Enfant, Fondation Chantal Biya, Yaoundé, CamerounUniversité Joseph Ravoahangy Andrianavalona, Antananarivo, MadagascarUniversité Sylvanus Olympio, Lomé, TogoGroupe Franco-Africain d'Oncologie Pédiatrique, Gustave Roussy, Villejuif, FranceGroupe Franco-Africain d'Oncologie Pédiatrique, Gustave Roussy, Villejuif, FrancePURPOSE: Multidisciplinary management of Wilms tumor has been defined through multicenter prospective studies and an average expected patient cure rate of 90%. In sub-Saharan Africa, such studies are uncommon. After the encouraging results of the first Groupe Franco-Africain d'Oncologie Pédiatrique (GFAOP) study, we report the results of the GFAOP-NEPHRO-02 study using an adaptation of the International Society of Paediatric Oncology 2001 protocol. PATIENTS AND METHODS: From April 1, 2005, to March 31, 2011, seven African units participated in a nonrandomized prospective study. All patients who were referred with a clinical and radiologic diagnosis of renal tumor were screened. Those older than age 6 months and younger than 18 years with a unilateral tumor previously untreated were pre-included and received preoperative chemotherapy. Patients with unfavorable histology or with a tumor other than Wilms, or with a nonresponding stage IV tumor were excluded secondarily. RESULTS: Three hundred thirteen patients were initially screened. Two hundred fifty-seven patients were pre-included and 169 with histologic confirmation of intermediate-risk nephroblastoma were registered in the study and administered postoperative treatment. Thirty-one percent of patients were classified as stage I, 38% stage II, 24% stage III, and 7% stage IV. Radiotherapy was not available for any stage III patients. Three-year overall survival rate was 72% for all study patients and 73% for those with localized disease. CONCLUSION: It was possible to conduct sub-Saharan African multicenter therapeutic studies within the framework of GFAOP. Survival results were satisfactory. Improvements in procedure, data collection, and outcome are expected in a new study. Radiotherapy is needed to reduce the relapse rate in patients with stage III disease.http://ascopubs.org/doi/10.1200/JGO.18.00204
collection DOAJ
language English
format Article
sources DOAJ
author Atteby Jean-Jacques Yao
Claude Moreira
Fousseyni Traoré
Sonia Kaboret
Angele Pondy
Mbolanirina Lala Rakotomahefa Narison
Koffi M. Guedenon
Brenda Mallon
Catherine Patte
spellingShingle Atteby Jean-Jacques Yao
Claude Moreira
Fousseyni Traoré
Sonia Kaboret
Angele Pondy
Mbolanirina Lala Rakotomahefa Narison
Koffi M. Guedenon
Brenda Mallon
Catherine Patte
Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
Journal of Global Oncology
author_facet Atteby Jean-Jacques Yao
Claude Moreira
Fousseyni Traoré
Sonia Kaboret
Angele Pondy
Mbolanirina Lala Rakotomahefa Narison
Koffi M. Guedenon
Brenda Mallon
Catherine Patte
author_sort Atteby Jean-Jacques Yao
title Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
title_short Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
title_full Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
title_fullStr Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
title_full_unstemmed Treatment of Wilms Tumor in Sub-Saharan Africa: Results of the Second French African Pediatric Oncology Group Study
title_sort treatment of wilms tumor in sub-saharan africa: results of the second french african pediatric oncology group study
publisher American Society of Clinical Oncology
series Journal of Global Oncology
issn 2378-9506
publishDate 2019-09-01
description PURPOSE: Multidisciplinary management of Wilms tumor has been defined through multicenter prospective studies and an average expected patient cure rate of 90%. In sub-Saharan Africa, such studies are uncommon. After the encouraging results of the first Groupe Franco-Africain d'Oncologie Pédiatrique (GFAOP) study, we report the results of the GFAOP-NEPHRO-02 study using an adaptation of the International Society of Paediatric Oncology 2001 protocol. PATIENTS AND METHODS: From April 1, 2005, to March 31, 2011, seven African units participated in a nonrandomized prospective study. All patients who were referred with a clinical and radiologic diagnosis of renal tumor were screened. Those older than age 6 months and younger than 18 years with a unilateral tumor previously untreated were pre-included and received preoperative chemotherapy. Patients with unfavorable histology or with a tumor other than Wilms, or with a nonresponding stage IV tumor were excluded secondarily. RESULTS: Three hundred thirteen patients were initially screened. Two hundred fifty-seven patients were pre-included and 169 with histologic confirmation of intermediate-risk nephroblastoma were registered in the study and administered postoperative treatment. Thirty-one percent of patients were classified as stage I, 38% stage II, 24% stage III, and 7% stage IV. Radiotherapy was not available for any stage III patients. Three-year overall survival rate was 72% for all study patients and 73% for those with localized disease. CONCLUSION: It was possible to conduct sub-Saharan African multicenter therapeutic studies within the framework of GFAOP. Survival results were satisfactory. Improvements in procedure, data collection, and outcome are expected in a new study. Radiotherapy is needed to reduce the relapse rate in patients with stage III disease.
url http://ascopubs.org/doi/10.1200/JGO.18.00204
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