Outcome of pediatric non-Hodgkin lymphoma in Central America: A report of the Association of Pediatric Hematology Oncology of Central America (AHOPCA).


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
05 2019
Historique:
received: 01 10 2018
revised: 04 01 2019
accepted: 07 01 2019
pubmed: 25 1 2019
medline: 18 12 2019
entrez: 25 1 2019
Statut: ppublish

Résumé

Treating B-non-Hodgkin lymphoma (B-NHL) in lower-income countries is challenging because of imprecise diagnosis, the increased risk of fatal toxicity associated with advanced disease at presentation, and limited supportive care. Central American patients with newly diagnosed stage I or II B-NHL received a modified Berlin-Frankfurt-Münster (BFM) regimen including a prephase (prednisone, cyclophosphamide) followed by A/B/A courses (A: cytarabine, dexamethasone, etoposide, ifosfamide, methotrexate, and intrathecal therapy; B: cyclophosphamide, dexamethasone, doxorubicin, methotrexate, and intrathecal therapy). Those with stage III or IV NHL received additional courses (B/A/B), intensified for stage IV disease by additional vincristine and methotrexate doses. Patients in poor condition received a second prephase treatment before their chemotherapy courses. Between March 2004 and June 2016, of 405 patients with B-NHL, 386 (109 females) were eligible for treatment. Immunohistochemistry was performed in 177 cases (47.4%) and characterized the disease as mature B-cell lymphoma. Stage distribution was as follows: I/II, 31 (8.1%); III, 252 (65.3%); IV, 93 (24.1%); 10 (2.6%) not available. The 3-year overall survival was 70% for the whole group (86% for stages I/II, 75% for stage III, 58% for stage IV). Events included death during induction (34 patients, 8.8%), relapse/progression (46, 11.9%), death in remission (9, 2.3%), second malignancy (1, 0.26%), and death of unknown cause (1, 0.26%). Twenty-three (6%) patients abandoned or refused therapy. Approximately 70% of children with B-NHL from Central America experienced long-term, disease-free survival with a modified BFM schedule. Toxic death and relapse/resistant disease were the main reasons for treatment failure.

Sections du résumé

BACKGROUND
Treating B-non-Hodgkin lymphoma (B-NHL) in lower-income countries is challenging because of imprecise diagnosis, the increased risk of fatal toxicity associated with advanced disease at presentation, and limited supportive care.
PROCEDURE
Central American patients with newly diagnosed stage I or II B-NHL received a modified Berlin-Frankfurt-Münster (BFM) regimen including a prephase (prednisone, cyclophosphamide) followed by A/B/A courses (A: cytarabine, dexamethasone, etoposide, ifosfamide, methotrexate, and intrathecal therapy; B: cyclophosphamide, dexamethasone, doxorubicin, methotrexate, and intrathecal therapy). Those with stage III or IV NHL received additional courses (B/A/B), intensified for stage IV disease by additional vincristine and methotrexate doses. Patients in poor condition received a second prephase treatment before their chemotherapy courses.
RESULTS
Between March 2004 and June 2016, of 405 patients with B-NHL, 386 (109 females) were eligible for treatment. Immunohistochemistry was performed in 177 cases (47.4%) and characterized the disease as mature B-cell lymphoma. Stage distribution was as follows: I/II, 31 (8.1%); III, 252 (65.3%); IV, 93 (24.1%); 10 (2.6%) not available. The 3-year overall survival was 70% for the whole group (86% for stages I/II, 75% for stage III, 58% for stage IV). Events included death during induction (34 patients, 8.8%), relapse/progression (46, 11.9%), death in remission (9, 2.3%), second malignancy (1, 0.26%), and death of unknown cause (1, 0.26%). Twenty-three (6%) patients abandoned or refused therapy.
CONCLUSIONS
Approximately 70% of children with B-NHL from Central America experienced long-term, disease-free survival with a modified BFM schedule. Toxic death and relapse/resistant disease were the main reasons for treatment failure.

Identifiants

pubmed: 30677231
doi: 10.1002/pbc.27621
pmc: PMC6428601
mid: NIHMS1006470
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27621

Subventions

Organisme : NCI NIH HHS
ID : P30 CA021765
Pays : United States
Organisme : NCI NIH HHS
ID : CA21765
Pays : United States

Informations de copyright

© 2019 Wiley Periodicals, Inc.

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Auteurs

Armando Peña-Hernandez (A)

Department of Pediatric Hemato-Oncology, Hospital Escuela-Universitario, Tegucigalpa, Honduras.

Roberta Ortiz (R)

Department of Pediatric Oncology, Manuel de Jésus Rivera Hospital, Managua, Nicaragua.

Claudia Garrido (C)

National Pediatric Oncology Unit, Francisco Marroquín University Medical School, Guatemala City, Guatemala.

Wendy Gomez-Garcia (W)

Department of Hematology-Oncology, Dr. Robert Reid Cabral Children's Hospital, Santo Domingo, Dominican Republic.

Soad Fuentes-Alabi (S)

Department of Onco-Hematology, Hospital Benjamin Bloom, San Salvador, El Salvador.

Roxana Martinez (R)

Hemato-Oncology Service, Hospital Mario Catarino Rivas, San Pedro Sula, Honduras.

Monika L Metzger (ML)

Department of Oncology, Leukemia/Lymphoma Division, and Global Pediatric Medicine Program, St. Jude Children's Research Hospital, Memphis, Tennessee.

Guillermo L Chantada (GL)

Hospital de Pediatría (SAMIC) Prof. Dr. Juan P. Garrahan, Buenos Aires, Argentina.

Raul C Ribeiro (RC)

Department of Oncology, Leukemia/Lymphoma Division, and Global Pediatric Medicine Program, St. Jude Children's Research Hospital, Memphis, Tennessee.

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