Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique

PURPOSE: To evaluate the results of an intensive polychemotherapy regimen for Burkitt lymphoma (BL) in sub-Saharan African pediatric centers. PATIENTS AND METHODS: Children with advanced-stage BL (stages II bulky, III, and IV) treated with the GFAOP–Lymphomes Malins B (GFALMB) 2009 protocol in 7 cen...

Full description

Bibliographic Details
Main Authors: Gabrielle C. Bouda, Fousseyni Traoré, Line Couitchere, Marie-Anne Raquin, Koffi M. Guedenon, Angele Pondy, Claude Moreira, Mbola Rakotomahefa, Mhamed Harif, Catherine Patte
Format: Article
Language:English
Published: American Society of Clinical Oncology 2019-12-01
Series:Journal of Global Oncology
Online Access:http://ascopubs.org/doi/10.1200/JGO.19.00172
_version_ 1828438259933380608
author Gabrielle C. Bouda
Fousseyni Traoré
Line Couitchere
Marie-Anne Raquin
Koffi M. Guedenon
Angele Pondy
Claude Moreira
Mbola Rakotomahefa
Mhamed Harif
Catherine Patte
author_facet Gabrielle C. Bouda
Fousseyni Traoré
Line Couitchere
Marie-Anne Raquin
Koffi M. Guedenon
Angele Pondy
Claude Moreira
Mbola Rakotomahefa
Mhamed Harif
Catherine Patte
author_sort Gabrielle C. Bouda
collection DOAJ
description PURPOSE: To evaluate the results of an intensive polychemotherapy regimen for Burkitt lymphoma (BL) in sub-Saharan African pediatric centers. PATIENTS AND METHODS: Children with advanced-stage BL (stages II bulky, III, and IV) treated with the GFAOP–Lymphomes Malins B (GFALMB) 2009 protocol in 7 centers between April 2009 and September 2015 were prospectively registered. Treatment regimen contained a prephase with cyclophosphamide followed by 2 induction courses (cyclophosphamide, vincristine, prednisone, high-dose methotrexate [HDMTX]), 2 consolidation courses (cytarabine, HDMTX), and a maintenance phase only for stage IV. HDMTX was given at the dose of 3 g/m2. RESULTS: Four hundred patients were analyzed: 7% had stage II bulky, 76% stage III, and 17% stage IV disease. Median age was 7.3 years, and sex ratio was 1.9:1 (male:female). A total of 221 patients received the whole protocol treatment and 195 achieved complete remission (CR), 11 of them after a second-line treatment. Treatment abandonment rate was 22%. One hundred twenty-five patients died, of whom 49 deaths were related to treatment toxicity. A total of 275 patients are alive, including 25 despite treatment abandonment, but only 110 are known to be in CR with a follow-up > 1 year, indicating a high rate of loss to follow-up. Twelve-month overall survival (OS) was 60% (95% CI, 54% to 66%) and 63%, 60%, and 31%, respectively, for stage II bulky, III, and IV. Patients with stage III disease who started second induction course within 34 days had OS of 76%, versus 57% (P = .0062) beyond 34 days. CONCLUSION: The GFA-LMB2009 protocol improved patients’ survival. Early dose intensity of treatment is a strong prognostic factor. Improving supportive care and decreasing loss to follow-up are crucial.
first_indexed 2024-12-10T20:00:28Z
format Article
id doaj.art-c5ba3683ce4f45398e089c874b6ffafd
institution Directory Open Access Journal
issn 2378-9506
language English
last_indexed 2024-12-10T20:00:28Z
publishDate 2019-12-01
publisher American Society of Clinical Oncology
record_format Article
series Journal of Global Oncology
spelling doaj.art-c5ba3683ce4f45398e089c874b6ffafd2022-12-22T01:35:32ZengAmerican Society of Clinical OncologyJournal of Global Oncology2378-95062019-12-0151910.1200/JGO.19.001721Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie PédiatriqueGabrielle C. Bouda0Fousseyni Traoré1Line Couitchere2Marie-Anne Raquin3Koffi M. Guedenon4Angele Pondy5Claude Moreira6Mbola Rakotomahefa7Mhamed Harif8Catherine Patte9CHU Yalgado Ouédraogo, Ouagadougou, Burkina FasoCHU Gabriel Touré, Bamako, MaliCHU de Treichville, Abidjan, Côte d’IvoireGustave Roussy Hospital and GFAOP Database Center, Villejuif, FranceCHU Sylvanus Olympio, Lomé, TogoCentre Mère-Enfant, Fondation Chantal Biya, Yaoundé, CamerounHôpital Aristide Le Dantec, Dakar, SénégalHJRA, Antananarivo, MadagascarHôpital 20 Août 1953, Casablanca, MoroccoGustave Roussy Hospital and GFAOP Database Center, Villejuif, FrancePURPOSE: To evaluate the results of an intensive polychemotherapy regimen for Burkitt lymphoma (BL) in sub-Saharan African pediatric centers. PATIENTS AND METHODS: Children with advanced-stage BL (stages II bulky, III, and IV) treated with the GFAOP–Lymphomes Malins B (GFALMB) 2009 protocol in 7 centers between April 2009 and September 2015 were prospectively registered. Treatment regimen contained a prephase with cyclophosphamide followed by 2 induction courses (cyclophosphamide, vincristine, prednisone, high-dose methotrexate [HDMTX]), 2 consolidation courses (cytarabine, HDMTX), and a maintenance phase only for stage IV. HDMTX was given at the dose of 3 g/m2. RESULTS: Four hundred patients were analyzed: 7% had stage II bulky, 76% stage III, and 17% stage IV disease. Median age was 7.3 years, and sex ratio was 1.9:1 (male:female). A total of 221 patients received the whole protocol treatment and 195 achieved complete remission (CR), 11 of them after a second-line treatment. Treatment abandonment rate was 22%. One hundred twenty-five patients died, of whom 49 deaths were related to treatment toxicity. A total of 275 patients are alive, including 25 despite treatment abandonment, but only 110 are known to be in CR with a follow-up > 1 year, indicating a high rate of loss to follow-up. Twelve-month overall survival (OS) was 60% (95% CI, 54% to 66%) and 63%, 60%, and 31%, respectively, for stage II bulky, III, and IV. Patients with stage III disease who started second induction course within 34 days had OS of 76%, versus 57% (P = .0062) beyond 34 days. CONCLUSION: The GFA-LMB2009 protocol improved patients’ survival. Early dose intensity of treatment is a strong prognostic factor. Improving supportive care and decreasing loss to follow-up are crucial.http://ascopubs.org/doi/10.1200/JGO.19.00172
spellingShingle Gabrielle C. Bouda
Fousseyni Traoré
Line Couitchere
Marie-Anne Raquin
Koffi M. Guedenon
Angele Pondy
Claude Moreira
Mbola Rakotomahefa
Mhamed Harif
Catherine Patte
Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
Journal of Global Oncology
title Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
title_full Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
title_fullStr Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
title_full_unstemmed Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
title_short Advanced Burkitt Lymphoma in Sub-Saharan Africa Pediatric Units: Results of the Third Prospective Multicenter Study of the Groupe Franco-Africain d’Oncologie Pédiatrique
title_sort advanced burkitt lymphoma in sub saharan africa pediatric units results of the third prospective multicenter study of the groupe franco africain d oncologie pediatrique
url http://ascopubs.org/doi/10.1200/JGO.19.00172
work_keys_str_mv AT gabriellecbouda advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT fousseynitraore advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT linecouitchere advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT marieanneraquin advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT koffimguedenon advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT angelepondy advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT claudemoreira advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT mbolarakotomahefa advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT mhamedharif advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique
AT catherinepatte advancedburkittlymphomainsubsaharanafricapediatricunitsresultsofthethirdprospectivemulticenterstudyofthegroupefrancoafricaindoncologiepediatrique