Wong Alison Y J, Marcotte Suzanne, Laroche Mathieu, Sheehan Nancy L, Kukreti Vishal, Routy Jean-Pierre, Lemieux Bernard, Seki Jack T, Rouleau Danielle, Tseng Alice
Chronic Viral Illness Service, McGill University Health Centre, Montréal, QC, Canada.
Antivir Ther. 2013;18(5):699-707. doi: 10.3851/IMP2572. Epub 2013 May 2.
Use of combination antiretroviral therapy (cART) and cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP) with or without rituximab for treatment of diffuse large B-cell lymphoma (DLBCL) in HIV substantially increases response rates but may also increase toxicity, possibly due to antiretroviral-antineoplastic drug interactions. The objective of this study was to evaluate the frequency of complete remission (CR) of DLBCL in patients treated with CHOP while receiving a protease inhibitor (PI) versus a non-PI-based cART.
A retrospective multicentre pilot study was conducted in HIV-infected patients on cART treated for DLBCL with CHOP between 2002-2010 in three academic hospitals.
A total of 34 patients were included with 65% and 35% of patients receiving a PI and non-PI-based cART, respectively. Baseline characteristics between groups were similar; overall 85% were male, median age was 43 years, 50% had an International Prognostic Index (IPI) of 2-3 and median CD4(+) T-cell count was 225 cells/mm(3). CR was achieved in 77% and 58% of patients in the PI and non-PI groups, respectively (P=0.21), with 65% and 63% of patients achieving 2-year overall survival (P=1.00). A multivariate analysis showed that lower IPI score alone was significantly associated with higher CR rates (P=0.05). Toxicity was similar between both groups.
Similar efficacy and toxicity of CHOP was observed in patients receiving a PI and non-PI-based cART.
使用联合抗逆转录病毒疗法(cART)以及环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP),无论是否联合利妥昔单抗来治疗HIV相关的弥漫性大B细胞淋巴瘤(DLBCL),虽可显著提高缓解率,但也可能增加毒性,这可能是由于抗逆转录病毒药物与抗肿瘤药物之间的相互作用所致。本研究的目的是评估在接受CHOP治疗的同时接受蛋白酶抑制剂(PI)与非基于PI的cART的DLBCL患者中完全缓解(CR)的频率。
2002年至2010年期间,在三家学术医院对接受cART治疗的HIV感染患者进行了一项回顾性多中心试点研究,这些患者采用CHOP治疗DLBCL。
共纳入34例患者,分别有65%和35%的患者接受基于PI和非基于PI的cART。两组之间的基线特征相似;总体上85%为男性,中位年龄为43岁,50%的国际预后指数(IPI)为2 - 3,中位CD4(+) T细胞计数为225个细胞/mm³。PI组和非PI组分别有77%和58%的患者实现CR(P = 0.21),65%和63%的患者实现2年总生存(P = 1.00)。多因素分析显示,仅较低的IPI评分与较高的CR率显著相关(P = 0.05)。两组之间的毒性相似。
在接受基于PI和非基于PI的cART的患者中,观察到CHOP的疗效和毒性相似。