Nondose-dense chemotherapy (EFT-2001) for pediatric Ewing sarcoma achieved a 3-year event-free survival of 65.3% (95% CI: 58.1-71.7%) and overall survival of 79.3% (95% CI: 72.8-84.5%).
Cohort (n=200)
Does a nondose-dense chemotherapy protocol provide feasible and effective outcomes for pediatric patients with Ewing sarcoma in resource-limited settings?
Nondose-dense chemotherapy provides feasible and effective outcomes with manageable toxicities for pediatric Ewing sarcoma in resource-limited settings, though cardiotoxicity remains a notable safety signal.
BACKGROUND: The current multidisciplinary approach in the treatment of Ewing sarcoma has improved cure rates, with contemporary dose-dense chemotherapy attaining 5-year event-free survival (EFS) of 73% in localized cases. Dose-intense and dose-dense chemotherapy is difficult in the majority of resource-limited settings with limited access to optimal supportive care. We report on patients with Ewing sarcoma treated on EFT-2001, a nondose-dense chemotherapy protocol. PROCEDURE: A retrospective analysis was conducted of patients (4 months (HR 3.42 95% CI: 1.32-8.89) affected outcomes. Nonrelapse mortality during treatment was 6.5%, mainly due to cardiomyopathy (3.0%) and bacterial sepsis (1.5%). Cardiotoxicity was seen in 11.5% of patients. CONCLUSIONS: Nondose-dense chemotherapy provides good outcomes with manageable toxicities in a multidisciplinary treatment approach, while reducing cumulative drug exposures in the developing world where dose-intense or dose-dense chemotherapy could potentially increase toxicity, and hence seems a feasible approach in resource-limited settings. Presence of any residual disease post definitive radiotherapy or delay in local control portends poor outcome.
Parambil et al. (Fri,) conducted a cohort in Ewing sarcoma (n=200). Nondose-dense chemotherapy (EFT-2001) was evaluated on 3-year event-free survival (EFS) (95% CI 58.1-71.7). Nondose-dense chemotherapy (EFT-2001) for pediatric Ewing sarcoma achieved a 3-year event-free survival of 65.3% (95% CI: 58.1-71.7%) and overall survival of 79.3% (95% CI: 72.8-84.5%).
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