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一项奥滨尤妥珠单抗或利妥昔单抗联合 CHOP 方案对比利妥昔单抗联合 CHOP 方案治疗初治弥漫性大 B 细胞淋巴瘤的随机、开放标签、III 期研究:GOYA 的最终分析。

A randomized, open-label, Phase III study of obinutuzumab or rituximab plus CHOP in patients with previously untreated diffuse large B-Cell lymphoma: final analysis of GOYA.

机构信息

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.

出版信息

J Hematol Oncol. 2020 Jun 6;13(1):71. doi: 10.1186/s13045-020-00900-7.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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%).

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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%)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91a5/7276080/9746e274293d/13045_2020_900_Fig1_HTML.jpg

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