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卡瑞利珠单抗联合卡铂和培美曲塞一线治疗晚期非鳞状 NSCLC:CameL Ⅲ期研究的扩展随访。

Camrelizumab Plus Carboplatin and Pemetrexed as First-Line Treatment for Advanced Nonsquamous NSCLC: Extended Follow-Up of CameL Phase 3 Trial.

机构信息

Department of Medical Oncology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, People's Republic of China.

Department of Respiratory Medicine, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.

出版信息

J Thorac Oncol. 2023 May;18(5):628-639. doi: 10.1016/j.jtho.2022.12.017. Epub 2023 Jan 13.

Abstract

INTRODUCTION

In CameL phase 3 study (ClinicalTrials.gov: NCT03134872), addition of camrelizumab to first-line chemotherapy significantly improved the progression-free survival in patients with stages IIIB to IV nonsquamous NSCLC. Here, we present outcomes after a minimum follow-up of 43.9 months since last patient randomization.

METHODS

Eligible patients were randomized 1:1 to 4 to 6 cycles of camrelizumab plus carboplatin and pemetrexed or chemotherapy alone every 3 weeks, followed by maintenance camrelizumab plus pemetrexed or pemetrexed only (n = 205 and 207, respectively). Total camrelizumab exposure was up to 2 years.

RESULTS

As of January 31, 2022, camrelizumab plus chemotherapy exhibited substantially improved overall survival over chemotherapy alone (median, 27.1 versus 19.8 mo; hazard ratio = 0.72 [95% confidence interval: 0.57-0.92]). In the chemotherapy-alone group, 95 patients (45.9%) crossed over to camrelizumab monotherapy. After adjustment for crossover, the survival benefit with camrelizumab plus chemotherapy was more pronounced (adjusted hazard ratio = 0.55 [95% confidence interval: 0.42-0.71]). In camrelizumab plus chemotherapy group, 33 patients completed 2 years of camrelizumab. Objective response rate was 97.0%, with ongoing responses in 17 of the 32 responses (53.1%), and 93.9% (31 of 33) of the patients were alive at data cutoff. Safety profiles were consistent with the previous report, and no obvious evidence of cumulative toxicity was found with long exposure to camrelizumab.

CONCLUSIONS

Camrelizumab plus carboplatin and pemetrexed provides long-term survival benefit over chemotherapy, with manageable toxicity and remarkable and durable response in patients receiving 2 years of camrelizumab, further supporting camrelizumab combination as first-line treatment for advanced nonsquamous NSCLC.

摘要

介绍

在 CameL 三期研究(ClinicalTrials.gov:NCT03134872)中,卡瑞利珠单抗联合一线化疗显著改善了 IIIB 期至 IV 期非鳞状 NSCLC 患者的无进展生存期。在此,我们报告了自最后一名患者随机分组后至少随访 43.9 个月的结果。

方法

符合条件的患者以 1:1 的比例随机分为两组,分别接受 4-6 个周期的卡瑞利珠单抗联合卡铂和培美曲塞或单纯化疗,每 3 周一次,随后接受卡瑞利珠单抗联合培美曲塞或培美曲塞维持治疗(分别为 205 例和 207 例)。总卡瑞利珠单抗暴露时间长达 2 年。

结果

截至 2022 年 1 月 31 日,卡瑞利珠单抗联合化疗组的总生存期明显长于单纯化疗组(中位,27.1 个月比 19.8 个月;风险比=0.72 [95%置信区间:0.57-0.92])。在单纯化疗组中,95 例患者(45.9%)交叉接受卡瑞利珠单抗单药治疗。调整交叉后,卡瑞利珠单抗联合化疗的生存获益更为显著(调整风险比=0.55 [95%置信区间:0.42-0.71])。在卡瑞利珠单抗联合化疗组中,33 例患者完成了 2 年的卡瑞利珠单抗治疗。客观缓解率为 97.0%,32 例缓解中 17 例仍在持续缓解(53.1%),数据截止时 93.9%(31 例)的患者存活。安全性特征与之前的报告一致,且长期暴露于卡瑞利珠单抗未发现明显的累积毒性证据。

结论

卡瑞利珠单抗联合卡铂和培美曲塞为晚期非鳞状 NSCLC 患者提供了长期生存获益,毒性可管理,且患者的缓解显著且持久,接受 2 年卡瑞利珠单抗治疗的患者获益更多,进一步支持卡瑞利珠单抗联合方案作为晚期非鳞状 NSCLC 的一线治疗。

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