医学
内科学
化疗
浆细胞白血病
沙利度胺
多元分析
白血病
肿瘤科
观察研究
骨髓
多发性骨髓瘤
作者
Camila Peña,Eloísa Riva,Natalia Schütz,Aline Ramírez,Jule Vásquez,Daniel Del Carpio-Jayo,Cristian Seehaus,Paola Ochoa,Rosa Vengoa,Patricio Duarte,Humberto Martínez-Cordero,Yrving Figueredo,Rosa Oliday Ríos,Jhoanna Ramírez,Virginia Bove,Macarena Roa,M. Russo,Marcela Espinoza,Gloritza Rodriguez,Guillermina Remaggi,María Elvira Enciso,Mauricio Chandía,Dorotea Fantl
标识
DOI:10.1080/10428194.2023.2171266
摘要
Primary plasma cell leukemia (pPCL) is an infrequent and aggressive plasma cell disorder. The prognosis is still very poor, and the optimal treatment remains to be established. A retrospective, multicentric, international observational study was performed. Patients from 9 countries of Latin America (LATAM) with a diagnosis of pPCL between 2012 and 2020 were included. 72 patients were included. Treatment was based on thalidomide in 15%, proteasome inhibitors (PI)-based triplets in 38% and chemotherapy plus IMIDs and/or PI in 29%. The mortality rate at 3 months was 30%. The median overall survival (OS) was 18 months. In the multivariate analysis, frontline PI-based triplets, chemotherapy plus IMIDs and/or PI therapy, and maintenance were independent factors of better OS. In conclusion, the OS of pPCL is still poor in LATAM, with high early mortality. PI triplets, chemotherapy plus IMIDs, and/or PI and maintenance therapy were associated with improved survival.
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