BC Cancer Centre for Lymphoid Cancer and the University of British Columbia, Vancouver, BC, Canada.
Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
J Hematol Oncol. 2020 Jun 6;13(1):71. doi: 10.1186/s13045-020-00900-7.
Rituximab (R) plus cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) is the current standard therapy for diffuse large B cell lymphoma (DLBCL). Obinutuzumab (G), a glycoengineered, type II anti-CD20 monoclonal antibody, has shown activity and an acceptable safety profile when combined with CHOP (G-CHOP) in patients with advanced DLBCL. We present the final analysis results of the Phase III GOYA study (NCT01287741), which compared the efficacy and safety of G-CHOP versus R-CHOP in patients with previously untreated DLBCL.
Patients aged ≥ 18 years with previously untreated advanced DLBCL were randomly assigned to receive eight 21-day cycles of R or G, plus six or eight cycles of CHOP. The primary endpoint was investigator-assessed progression-free survival (PFS). Secondary endpoints included overall survival, other time-to-event endpoints, and safety; investigator-assessed PFS by cell of origin subgroup was an exploratory endpoint.
A total of 1418 patients were randomized, with 1414 included in this final analysis (G-CHOP, N = 704; R-CHOP, N = 710). Five-year PFS rates were 63.8% and 62.6% for G-CHOP and R-CHOP, respectively (stratified hazard ratio 0.94, 95% CI 0.78-1.12; p = 0.48). The results of the secondary efficacy endpoints did not show a benefit of G-CHOP over R-CHOP. In the exploratory analysis, a trend towards benefit with G-CHOP over R-CHOP was apparent in the patients with germinal center B cell DLBCL. The safety profile of G-CHOP was as expected, and no new safety signals were observed. More grade 3-5 (75.1% vs 65.8%), serious (44.4% vs 38.4%), and fatal (6.1% vs 4.4%) adverse events (AEs) were observed in the G-CHOP arm compared with the R-CHOP arm, respectively, with the most common fatal AEs being infections. A higher incidence of late-onset neutropenia occurred in the G-CHOP arm (8.7%) versus the R-CHOP arm (4.9%).
The final analysis, similar to the primary analysis, did not show a PFS benefit of G-CHOP over R-CHOP in previously untreated patients with DLBCL. The results of the secondary endpoints were consistent with the primary endpoint. Further exploratory analyses and investigation of biomarkers are ongoing.
利妥昔单抗(R)联合环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)是弥漫性大 B 细胞淋巴瘤(DLBCL)的现行标准治疗方法。奥滨尤妥珠单抗(G),一种糖基化工程、II 型抗 CD20 单克隆抗体,与 CHOP(G-CHOP)联合用于晚期 DLBCL 患者时,显示出疗效和可接受的安全性。我们报告了 III 期 GOYA 研究(NCT01287741)的最终分析结果,该研究比较了初治 DLBCL 患者中 G-CHOP 与 R-CHOP 的疗效和安全性。
年龄≥18 岁、未经治疗的晚期 DLBCL 患者被随机分配接受 8 个 21 天周期的 R 或 G,加 6 或 8 个周期的 CHOP。主要终点为研究者评估的无进展生存期(PFS)。次要终点包括总生存期、其他时间相关终点和安全性;细胞起源亚组的研究者评估 PFS 是探索性终点。
共纳入 1418 例患者,最终分析纳入 1414 例(G-CHOP 组,N=704;R-CHOP 组,N=710)。G-CHOP 和 R-CHOP 的 5 年 PFS 率分别为 63.8%和 62.6%(分层风险比 0.94,95%CI 0.78-1.12;p=0.48)。次要疗效终点的结果未显示 G-CHOP 优于 R-CHOP。在探索性分析中,G-CHOP 似乎优于 R-CHOP,在生发中心 B 细胞 DLBCL 患者中表现出获益趋势。G-CHOP 的安全性特征与预期一致,未观察到新的安全性信号。G-CHOP 组与 R-CHOP 组相比,3-5 级(75.1%比 65.8%)、严重(44.4%比 38.4%)和致命(6.1%比 4.4%)不良事件(AE)更多,AE 最常见的是感染。G-CHOP 组迟发性中性粒细胞减少症的发生率高于 R-CHOP 组(8.7%比 4.9%)。
与主要分析相似,该最终分析未显示初治 DLBCL 患者中 G-CHOP 与 R-CHOP 相比,PFS 有获益。次要终点的结果与主要终点一致。正在进行进一步的探索性分析和生物标志物研究。