Liang Ze-yin, Cen Xi-nan, Qiu Zhi-xiang, Ou Jin-ping, Wang Wen-sheng, Xu Wei-lin, Li Yuan, Wang Mang-ju, Dong Yu-jun, Wang Li-hong, Yin Yue, Sun Yu-hua, Liu Wei, Wang Qian, Ren Han-yun
Department of Hematology, Peking University First Hospital, Beijing 100034, China.
Zhonghua Xue Ye Xue Za Zhi. 2012 Dec;33(12):1033-7.
This study was aimed to investigate whether incorporation of rituximab into high-dose chemotherapy with autologous peripheral blood stem cell transplantation (auto-PBSCT)could improve the survival of patients with diffuse large B-cell lymphoma (DLBCL), and evaluate the safety of this regimen.
Twenty-five patients (age, 17 - 61 yrs) with DLBCL were treated with a sequential chemotherapy for remission induction, intensive chemotherapy for mobilization of stem cells, and high-dose chemotherapy followed by auto-PBSCT. Among 25 patients, 22 cases were at IV Ann Arbor stage, 60% cases with B symptom, and 10 cases with intermediate-high risk and 2 cases with high risk when evaluated by International Prognostic Index (IPI). The high-dose chemotherapy included BEAM regimen for 21 patients, and TBI conditioning regimen for 4 patients. Each patient received infusion of rituximab at a dose of 375 mg/m(2) for 2 times, each at peripheral blood stem cell mobilization and peripheral stem cell infusion.
20 patients achieved complete remission (CR) before transplantation. After high-dose chemotherapy and auto-PBSCT, 92% patients achieved CR. At a median follow-up of 45 months, the estimated 3-year overall survival (OS) and progression-free survival (PFS) were 78.9% and 75.9%, respectively, for all patients; while those were 87.4% and 82.4% for patients achieved CR before auto-PBSCT. Multivariate analysis by Cox regression revealed that failure to achieving CR before auto-PBSCT was an independent prognostic factor affecting OS, while factor affecting PFS was IPI scores. Rituximab was generally well tolerated with few side-effects.
Our results suggested that the addition of rituximab to high-dose chemotherapy followed by auto-PBSCT was effective and safe for patients with DLBCL.
本研究旨在探讨将利妥昔单抗纳入大剂量化疗联合自体外周血干细胞移植(auto-PBSCT)是否能提高弥漫性大B细胞淋巴瘤(DLBCL)患者的生存率,并评估该方案的安全性。
25例年龄在17至61岁之间的DLBCL患者接受序贯化疗以诱导缓解、强化化疗以动员干细胞,随后进行大剂量化疗及auto-PBSCT。25例患者中,22例处于Ann Arbor分期IV期,60%有B症状,根据国际预后指数(IPI)评估,10例为中高危,2例为高危。21例患者接受BEAM方案大剂量化疗,4例接受全身照射预处理方案。每位患者在动员外周血干细胞和输注外周干细胞时各接受1次剂量为375mg/m²的利妥昔单抗输注。
20例患者在移植前达到完全缓解(CR)。大剂量化疗及auto-PBSCT后,92%的患者达到CR。中位随访45个月时,所有患者的3年总生存率(OS)和无进展生存率(PFS)估计分别为78.9%和75.9%;而auto-PBSCT前达到CR的患者分别为87.4%和82.4%。Cox回归多因素分析显示,auto-PBSCT前未达到CR是影响OS的独立预后因素,而影响PFS的因素是IPI评分。利妥昔单抗总体耐受性良好,副作用较少。
我们的结果表明,在大剂量化疗联合auto-PBSCT基础上加用利妥昔单抗对DLBCL患者有效且安全。