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奥滨尤妥珠单抗对比利妥昔单抗用于晚期弥漫性大 B 细胞淋巴瘤:LYSA 的一项基于 PET 指导的随机 3 期研究。

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

机构信息

Service d'Hématologie, Clinique du Centre Hospitalier Universitaire (CHU) de Nantes, Nantes, France.

Center for Research in Cancerology and Immunology Nantes/Angers (CRCINA), Nantes, France.

出版信息

Blood. 2021 Apr 29;137(17):2307-2320. doi: 10.1182/blood.2020008750.

Abstract

Rituximab plus polychemotherapy 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 immunochemotherapy. Responders after only cycle 4 (PET2+/4-) received transplantation. The primary objective was an 8% improvement (hazard ratio [HR] = 0.73; 80% power; α risk, 2.5%; 1-sided) in 2-year event-free survival (EFS) in the obinutuzumab arm. From September 2012, 670 patients were enrolled (obinutuzumab, n = 336; rituximab, n = 334). 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 = 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. This trial was registered at www.clinicaltrials.gov as #NCT01659099.

摘要

奥滨尤妥珠单抗对比利妥昔单抗用于初治年龄调整国际预后指数(aaIPI)≥1 弥漫性大 B 细胞淋巴瘤(DLBCL)患者的疗效:GAINED 是一项随机 3 期临床试验

在这项研究中,年龄在 18 岁至 60 岁之间、未经治疗且 aaIPI 评分≥1 的 DLBCL 患者,按照 1:1 的比例随机分为奥滨尤妥珠单抗组或利妥昔单抗组,分层因素包括 aaIPI(1;2-3)和化疗方案(多柔比星、环磷酰胺、泼尼松联合长春新碱、博来霉素[ACVBP]或长春新碱[CHOP])。根据中期正电子发射断层扫描(PET)的应答情况确定巩固治疗方案。2 个周期和 4 个周期后(PET2-/PET4-)应答的患者接受免疫化疗。仅在 4 个周期后(PET2+/4-)应答的患者接受移植。主要终点是奥滨尤妥珠单抗组 2 年无事件生存率(EFS)较利妥昔单抗组提高 8%(风险比 [HR] = 0.73;80%效能;α 风险,2.5%;单侧)。从 2012 年 9 月开始,共纳入 670 例患者(奥滨尤妥珠单抗组,n=336;利妥昔单抗组,n=334)。其中,57.2%为 aaIPI 2-3 患者,50.6%接受 CHOP 方案治疗。中位随访时间为 38.7 个月。两组 2 年 EFS 相似(59.8% vs 56.6%;P=0.123;HR=0.88)。全队列患者的 2 年无进展生存率(PFS)为 83.1%(95%置信区间,80%~85.8%)。PET2-/4-和 PET2+/4-患者的 2 年无进展生存(PFS)和总生存(OS)相似:89.9% vs 83.9%和 94.8% vs 92.8%。PET4+患者的 2 年 PFS 和 OS 分别为 62%和 83.1%。奥滨尤妥珠单抗组 3-5 级感染的发生率高于利妥昔单抗组(21% vs 12%)。在 aaIPI≥1 的 DLBCL 可移植患者中,奥滨尤妥珠单抗并不优于利妥昔单抗。该研究在 www.clinicaltrials.gov 注册,编号为 #NCT01659099。

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