| Literature DB >> 31774004 |
Kalasekhar Vijayasekharan1,2, Maya Prasad1,2, Nirmalya D Pradhan1,2, Deepa Phillip1,2, Sumeet Gujral1,2, Tanuja Shet1,2, Epari Sridhar1,2, Seema Kembhavi1,2, Sneha Shah1,2, Shripad D Banavali1,2, Gaurav Narula1,2.
Abstract
Anaplastic large cell lymphoma (ALCL) is a rare form of non-Hodgkin lymphoma (NHL) in children. Most treatment regimens include high-dose methotrexate (HDMTX), which is logistically difficult to administer in resource-limited settings. We evaluated the outcomes of pediatric ALCL patients treated on a uniform protocol (Modified Multicentric Protocol, MCP-842 regimen) at our hospital between January 2005 and December 2016. Of the 68 patients who received treatment on the Modified MCP842 protocol, 46 patients are alive in remission, 11(16%) had disease progression, 9(13%) relapsed after achieving remission, and 5(7%) had treatment-related mortality (TRM). Seventeen of 20 relapsed/progressed patients subsequently expired. With a median follow-up of 55 months (range 2-165 months), the 4-year event-free survival (EFS) and overall survival (OS) are 63% (95% CI of 50-73%) and 70%(95% CI of 57-79%), respectively. An indigenous protocol using vinblastine (without HDMTX and steroids) is feasible in a resource-limited setting and achieves outcomes comparable to regimens incorporating HDMTX, with lower toxicity.Entities:
Keywords: Pediatric ALCL; outcomes; vinblastine
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Year: 2019 PMID: 31774004 DOI: 10.1080/10428194.2019.1695054
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022