Results of the Latin American Pediatric Oncology Group (GALOP) Trial for Patients With Metastatic Ewing Sarcoma: Multicentric Study of Interval‐Compressed Multiagent and Metronomic Chemotherapy

Author:

Rose Adriana1,Gregianin Lauro Jose2,Boldrini Erica3,Macedo Carla4,Ferman Sima5,Costa Tatiana El Jaick Bonifácio6,Scopinaro Marcelo7,Brunetto Algemir Lunardi8,Brunetto André Tesainer8ORCID,Villarroel Milena9,

Affiliation:

1. Hospital de Pediatría Dr J.P. Garrahan Buenos Aires Argentina

2. Hospital de Clínicas de Porto Alegre Porto Alegre Brazil

3. Hospital de Amor Barretos Brazil

4. Instituto de Oncologia Pediátrica São Paulo Brazil

5. Instituto Nacional de Câncer Rio de Janeiro Brazil

6. Hospital Infantil Joana de Gusmão Florianópolis Brazil

7. Hospital de Pediatria SAMIC Prof° “Dr Juan Garrahan Buenos Aires Argentina

8. Instituto do Câncer Infantil Porto Alegre Brazil

9. Hospital Dr. Luis Calvo Mackenna Providencia Chile

Abstract

ABSTRACTBackgroundGALOP investigators developed a multicenter protocol to standardize treatment for newly diagnosed metastatic Ewing sarcoma (ES) in South America.MethodsProspective trial. Induction chemotherapy consisted of 9 alternating interval‐compressed cycles (every 14 days) of vincristine, doxorubicin, cyclophosphamide, and ifosfamide–etoposide; local and metastatic site control; and 5 consolidation cycles (every 21 days), followed by MCT with cyclophosphamide and vinblastine for 1 year.ResultsBetween 2011 and 2019, 198 patients were recruited from 34 centers in Argentina, Brazil, Chile, and Uruguay. Characteristics include: male patients (60.6%), median age of 12.3 years (range, 0.8–31.1); axial primary localization (62.1%), size >8 cm (70.2%); and bone origin (71.2%). Metastatic sites were lung, extra‐lung, and combined in 43.4%, 31.3%, and 25.3%, respectively. The overall response rate was 79.3%, and local treatment was performed in 85.3% of patients. With a median follow‐up of 65.1 months (95% CI: 53.9–76.4), the 5‐year overall survival (OS) and event‐free survival (EFS) were 33.1% (95% CI: 25.9–40.4) and 27.8% (95% CI: 21.5–34.3), respectively. The 5‐year OS was 44.9%, 31.3%, and 15.6% for lung, extra‐lung, and combined, respectively (p < 0.001). The median interval between induction chemotherapy cycles was 17 days, with a febrile neutropenia rate of 19.3%. Metronomic chemotherapy (MCT) was administered to 100 patients (50.5%), demonstrating good tolerability, with 58 patients completing at least 75% of the scheduled cycles.ConclusionThe implementation of a multicenter protocol incorporating MCT for metastatic ES proved feasible across Latin America.

Publisher

Wiley

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