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Anaplastic Large Cell Lymphoma in Central America: A Report From the Central American Association of Pediatric Hematology Oncology (AHOPCA).
Ceppi, Francesco; Ortiz, Roberta; Antillón, Federico; Vasquez, Roberto; Gomez, Wendy; Gamboa, Jessica; Garrido, Claudia; Chantada, Guillermo; Peña, Armando; Gupta, Sumit.
Afiliação
  • Ceppi F; Division of Haematology/Oncology, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Ortiz R; Department of Pediatric Oncology, Manuel de Jesus Rivera Hospital, Managua, Nicaragua.
  • Antillón F; National Pediatric Oncology Unit, Francisco Marroquín Medical School, Guatemala City, Guatemala.
  • Vasquez R; Department of Onco-Hematology, Hospital Benjamin Bloom, San Salvador, El Salvador.
  • Gomez W; Department of Hematology-Oncology, Dr. Robert Reid Cabral Children's Hospital, Santo Domingo, Dominican Republic.
  • Gamboa J; Department of Hematology-Oncology, Hospital Nacional de Niños "Dr. Carlos Sáenz Herrera", San José, Costa Rica.
  • Garrido C; National Pediatric Oncology Unit, Francisco Marroquín Medical School, Guatemala City, Guatemala.
  • Chantada G; Department of Hemato-oncology, Hospital JP Garrahan, Buenos Aires, Argentina.
  • Peña A; International Outreach Program, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Gupta S; Department of Pediatric Hemato-Oncology, Hospital Escuela-Universitario, Tegucigalpa, Honduras.
Pediatr Blood Cancer ; 63(1): 78-82, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26257093
ABSTRACT

BACKGROUND:

Although anaplastic large cell lymphoma (ALCL) is curable in high-income countries (HIC), data from low- and middle-income countries (LMIC) are lacking. We therefore conducted a retrospective study of the Central American Association of Pediatric Hematology Oncology (AHOPCA) experience in treating ALCL. PROCEDURE We included all patients age <18 years newly diagnosed with ALCL treated between 2000 and 2013 in seven AHOPCA institutions. Retrospective data were extracted from the Pediatric Oncology Network Database.

RESULTS:

Thirty-one patients met inclusion criteria. Twenty-five (81%) had advanced disease (stages III and IV), six (19%) were treated on the APO (doxorubicin, prednisone, vincristine) regimen, 15 (49%) on multi-agent chemotherapy designed for T-cell lineage malignancies (GuatALCL protocol), and 10 (32%) on BFM-based treatment regimens. Five-year overall event-free survival and overall survival were, respectively, 67.1 ± 8.6% and 66.7 ± 8.7%. All 10 events occurred in patients treated on BFM-based treatment regimens or the GuatALCL protocol, none on APO treatment two patients experienced relapse, six treatment related mortality (TRM), and two abandonment.

CONCLUSIONS:

Treatment of ALCL in countries with limited resources is feasible with similar outcomes as in HIC, though the causes of treatment failure differ. Less intensive regimens may be preferable in order to decrease TRM and improve outcomes. Prospective clinical trials determining the ideal treatment for LMIC children with ALCL are necessary.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Anaplásico de Células Grandes Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: America central Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Anaplásico de Células Grandes Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: America central Idioma: En Ano de publicação: 2016 Tipo de documento: Article