Treatment of high‐risk Hodgkin lymphoma with a modified Stanford V regimen in the AHOPCA: Substituting chemotherapy agents and hampered outcomes

Author:

Luna‐Fineman Sandra123ORCID,Castellanos Mauricio2,Metzger Monika L.4,Baez L. Fulgencio5,Peña Hernandez Armando6,Bonilla Miguel3,Fuentes‐Alabi Soad7,Nieves Rosa8,Blanco Jessica29,Rossi Emanuela9,Devidas Meenakshi3,Chen Yichen3,Arreola Magda2,de Alarcon Pedro A.10

Affiliation:

1. Hematology/Oncology/SCT, Department of Pediatrics University of Colorado Aurora Colorado USA

2. Unidad Nacional de Oncología Pediátrica (UNOP) Guatemala Guatemala

3. Global Pediatric Medicine St Jude Children's Research Hospital Memphis Tennessee USA

4. Médecins sans Frontières Geneva Switzerland

5. Oncología Pediátrica Hospital Manuel de Jesús Rivera "La Mascota" Managua Nicaragua

6. Oncología Pediátrica Hospital Escuela Universitario Materno Infantil Tegucigalpa Honduras

7. Oncología Pediátrica Hospital de Niños Benjamín Bloom, Centro Médico "Ayúdame a Vivir" San Salvador El Salvador

8. Oncología Pediátrica Hospital Infantil Dr. Robert Reid Cabral Santo Domingo Dominican Republic

9. Center for Biostatistics for Clinical Epidemiology, School of Medicine and Surgery University of Milano‐Bicocca Milan Italy

10. Department of Pediatrics University of Illinois College of Medicine and St Jude Midwest Affiliate Children's Hospital of Illinois Peoria Illinois USA

Abstract

AbstractBackground/objectivesHigh‐risk Hodgkin lymphoma (HRHL) in children is curable with combined modality therapy. The Association of Pediatric Hematology‐Oncology of Central America (AHOPCA) is a consortium of cancer centers from Central America. In 2004, AHOPCA implemented a guideline with a short course of chemotherapy (mStanfordV), strict diagnostics, and radiation guidelines, aimed at reducing abandonment and improving outcomes.MethodsNewly diagnosed children less than 18 years of age with high‐risk HL (Ann Arbor stages: IIB, IIIB, IV) from AHOPCA centers were staged with chest radiography and ultrasound or computed tomography. Therapy was a modified Stanford V (mStanfordV), substituting cyclophosphamide for mechlorethamine and involved field radiation.ResultsOf 219 patients with HRHL, 181 patients were eligible and evaluable; 146 (81%) were boys, 22% being less than 6 years; 43 were stage IIB, 84 IIIB, and 54 IV. Thirty‐one (17%) abandoned therapy, 28 (15%) progressed, 30 (17%) relapsed, and eight (4%) died of toxicity. Radiation guidelines were not followed. Five‐year abandonment‐sensitive event‐free survival and overall survival (AS‐EFS, AS‐OS ± SE) for the cohort were 46% ± 4% and 56% ± 4%; 5‐year AS‐OS for stages IIB, IIIB, and IV was 76% ± 7%, 59% ± 7%, and 35% ± 7% (p = .0006).ConclusionDespite instituting a short treatment guideline, it did not improve the abandonment rate (17%) and did not achieve the reported outcomes of Stanford V. The cyclophosphamide dose used to replace merchlorethamine was inadequate. Despite strict guidelines, the radiation therapy application was inaccurate. Weekly chemotherapy may have adversely affected abandonment of therapy by increasing the burden of travel time. Based on these results, AHOPCA established a new abandonment strategy and a new guideline.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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