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卡瑞利珠单抗联合培美曲塞和卡铂一线治疗伴脑转移的晚期非鳞状非小细胞肺癌(CAP-BRAIN)的疗效、安全性和与健康相关的生活质量:一项多中心、开放标签、单臂、Ⅱ期研究。

Efficacy, Safety, and Health-Related Quality of Life With Camrelizumab Plus Pemetrexed and Carboplatin as First-Line Treatment for Advanced Nonsquamous NSCLC With Brain Metastases (CAP-BRAIN): A Multicenter, Open-Label, Single-Arm, Phase 2 Study.

机构信息

Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, People's Republic of China; State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, People's Republic of China.

State Key Laboratory of Respiratory Disease, National Clinical Research Centre for Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, People's Republic of China.

出版信息

J Thorac Oncol. 2023 Jun;18(6):769-779. doi: 10.1016/j.jtho.2023.01.083. Epub 2023 Feb 2.

DOI:10.1016/j.jtho.2023.01.083
PMID:36738928
Abstract

INTRODUCTION

Systemic treatment options for NSCLC with brain metastases (BMs) are scarce. We evaluated the activity and safety of camrelizumab plus chemotherapy as first-line therapy in patients with advanced nonsquamous NSCLC with BMs.

METHODS

This was a multicenter, single-arm, phase 2 trial (NCT04211090) conducted at seven hospitals in China. Eligible patients had treatment-naive metastatic nonsquamous NSCLC and BMs that were asymptomatic or symptoms controlled with dehydration therapy and no previous systemic treatment or local therapy for the target brain lesion. Patients received camrelizumab (200 mg) plus pemetrexed (500 mg/m) and carboplatin (area under the curve 5) intravenously on day 1 of each 21-day cycle for four cycles, followed by maintenance with camrelizumab (200 mg) and pemetrexed (500 mg/m) every 21 days until disease progression, unacceptable toxicity, or death. The primary end point was confirmed intracranial objective response rate according to modified Response Evaluation Criteria in Solid Tumors version 1.1, which was primarily analyzed in the efficacy analysis set (EAS).

RESULTS

A total of 45 patients were enrolled and treated (full analysis set), with 40 patients having at least one post-baseline tumor assessment (EAS). As of August 30, 2022, median follow-up duration was 12.5 months (95% confidence interval [CI]: 9.2-17.3). The confirmed intracranial objective response rate was 52.5% (95% CI: 36.1-68.5) in EAS and 46.7% (95% CI: 31.7-62.1) in full analysis set. The extracranial objective response rate was 47.5% (95% CI: 31.5-63.9) and 42.2% (95% CI: 27.7-57.8), respectively. Median intracranial progression-free survival was 7.6 months (95% CI: 4.6-not reached [NR]), median overall progression-free survival was 7.4 months (95% CI: 4.4-NR), and median overall survival was 21.0 months (95% CI: 15.9-NR). The most common treatment-related adverse events of grade 3 or higher were neutrophil count decrease (six [13.3%]) and anemia (four [8.9%]). One treatment-related death occurred owing to immune-related pneumonia. Linear mixed-effects model displayed that a positive trend for improvement in cognitive function and quality of life was observed based on Montreal Cognitive Assessment and Functional Assessment of Cancer Therapy-Lung scores (p = 0.025, p < 0.001).

CONCLUSIONS

Camrelizumab plus pemetrexed and carboplatin was found to have an activity with manageable toxicity and to improve cognitive function and quality of life for patients with nonsquamous NSCLC with BMs in the first-line setting.

摘要

简介

患有脑转移(BMs)的非小细胞肺癌(NSCLC)的全身治疗选择有限。我们评估了卡瑞利珠单抗联合化疗作为伴 BMs 的晚期非鳞状 NSCLC 患者一线治疗的疗效和安全性。

方法

这是一项在中国 7 家医院进行的多中心、单臂、II 期临床试验(NCT04211090)。纳入的患者为初治转移性非鳞状 NSCLC 伴 BMs,无症状或经脱水治疗控制症状,且无既往用于目标脑转移病灶的全身治疗或局部治疗。患者接受卡瑞利珠单抗(200mg)联合培美曲塞(500mg/m2)和卡铂(曲线下面积 5)静脉滴注,每 21 天为一个周期,连用 4 个周期,随后每 21 天给予卡瑞利珠单抗(200mg)和培美曲塞(500mg/m2)维持治疗,直至疾病进展、不可接受的毒性或死亡。主要终点为根据实体瘤反应评价标准 1.1 版(mRECIST)修订版评估的确认颅内客观缓解率,主要在疗效分析集(EAS)中进行分析。

结果

共纳入 45 例患者并进行了治疗(全分析集),40 例患者至少有一次基线后肿瘤评估(EAS)。截至 2022 年 8 月 30 日,中位随访时间为 12.5 个月(95%置信区间[CI]:9.2-17.3)。EAS 中确认的颅内客观缓解率为 52.5%(95%CI:36.1-68.5),全分析集为 46.7%(95%CI:31.7-62.1)。EAS 和全分析集的颅外客观缓解率分别为 47.5%(95%CI:31.5-63.9)和 42.2%(95%CI:27.7-57.8)。颅内无进展生存期中位值为 7.6 个月(95%CI:4.6-NR),总无进展生存期中位值为 7.4 个月(95%CI:4.4-NR),总生存期中位值为 21.0 个月(95%CI:15.9-NR)。最常见的 3 级及以上治疗相关不良事件为中性粒细胞计数减少(6 例[13.3%])和贫血(4 例[8.9%])。1 例治疗相关死亡归因于免疫相关性肺炎。线性混合效应模型显示,基于蒙特利尔认知评估和癌症治疗-肺功能评估量表(Functional Assessment of Cancer Therapy-Lung,FACT-L),认知功能和生活质量有改善的趋势(p=0.025,p<0.001)。

结论

卡瑞利珠单抗联合培美曲塞和卡铂在伴 BMs 的非鳞状 NSCLC 患者的一线治疗中具有较好的疗效和可管理的毒性,可改善患者的认知功能和生活质量。

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