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Obinutuzumab vs rituximab for advanced DLBCL: a PET-guided and randomized phase 3 study by LYSA

机译:ObInutuzumab vs Rituximab用于高级DLBCL:Lysa的宠物引导和随机阶段3研究

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摘要

Rituximab plus p olychemotherapy is the standard of care in diffuse large B-cell lymphoma (DLBCL). GAINED, a randomized phase 3 trial, compared obinutuzumab to rituximab. Transplant-eligible patients (18-60 years) with an untreated age-adjusted International Prognostic Index (aaIPI) score >= 1 DLBCL were randomized (1:1) between obinutuzumab or rituximab and stratified by aaIPI (1; 2-3) and chemotherapy regimen (doxorubicin, cyclophosphamide, prednisone plus vindesine, bleomycin [ACVBP] or vincristine [CHOP]). Consolidation treatment was determined according to response to interim positron emission tomography (PET). Responders after cycle 2 and 4 (PET2(-)/PET4(-)) received immunoche-motherapy. Responders after only cycle 4 (PET2(-)/4(+)) received transplantation. The primary objective was an 8% improvement (hazard ratio [HR] = 0.73; 80% power; alpha risk, 2.5%; 1-sided) in 2-year event-free survival (EFS) in the obinutuzumab arm. From September 2012, 670 patientswere enrolled (obinutuzumab, n5336; rituximab, n5334). A total of 383 (57.2%) were aaIPI 2-3, 339 (50.6%) received CHOP. Median follow-up was 38.7 months. The 2-year EFS was similar in both groups (59.8% vs 56.6%; P =.123; HR 5 0.88). The 2-year PFS in the whole cohort was 83.1% ( 95% confidence interval, 80% to 85.8%). PET2(-)/4(-) and PET2(+)/4(-) had similar 2-year progression-free survival (PFS) and overall survival (OS): 89.9% vs 83.9% and 94.8% vs 92.8%. The 2-year PFS and OS for PET4(+) patients were 62% and 83.1%. Grade 3-5 infections were more frequent in the obinutuzumab arm (21% vs 12%). Obinutuzumab is not superior to rituximab in aaIPI >= 1 DLBCL transplant-eligible patients.
机译:利妥昔单抗联合化疗是弥漫性大B细胞淋巴瘤(DLBCL)的标准治疗方案。这是一项随机的3期试验,比较了奥比努珠单抗和利妥昔单抗。未经治疗的年龄调整国际预后指数(aaIPI)评分>=1 DLBCL的符合移植条件的患者(18-60岁)在奥比努珠单抗或利妥昔单抗之间随机(1:1),并按aaIPI(1;2-3)和化疗方案(阿霉素、环磷酰胺、强的松加长春地辛、博莱霉素[ACVBP]或长春新碱[CHOP])分层。根据中期正电子发射断层扫描(PET)的反应确定巩固治疗。第2和第4周期后的应答者(PET2(-)/PET4(-)接受免疫母婴疗法。仅第4周期(PET2(-)/4(+))后的应答者接受移植。主要目标是奥比努图珠单抗组2年无事件生存率(EFS)提高8%(危险比[HR]=0.73;80%功率;α风险,2.5%;单侧)。从2012年9月起,共有670名患者入选(obinutuzumab,n5336;利妥昔单抗,n5334)。共有383例(57.2%)为aaIPI 2-3,339例(50.6%)为CHOP。中位随访时间为38.7个月。两组的2年EFS相似(59.8%对56.6%;P=0.123;HR50.88)。整个队列的2年PFS为83.1%(95%可信区间,80%至85.8%)。PET2(-)/4(-)和PET2(+)/4(-)的2年无进展生存率(PFS)和总生存率(OS)相似:89.9%对83.9%,94.8%对92.8%。PET4(+)患者的2年PFS和OS分别为62%和83.1%。obinutuzumab组的3-5级感染更常见(21%对12%)。在aaIPI>=1例DLBCL移植合格患者中,奥比努珠单抗并不优于利妥昔单抗。

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