PD-1 inhibitor combined with albumin paclitaxel and apatinib as second-line treatment for patients with metastatic gastric cancer: a single-center, single-arm, phase II study.

IF 3 3区 医学 Q2 ONCOLOGY
Investigational New Drugs Pub Date : 2024-04-01 Epub Date: 2024-02-12 DOI:10.1007/s10637-024-01425-3
Miaomiao Gou, Yong Zhang, Zhikuan Wang, Niansong Qian, Guanghai Dai
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引用次数: 0

Abstract

Background: Immune checkpoint inhibitors have been approved for first- and third-line treatment of advanced gastric cancer. However, pembrolizumab alone in the second line did not improve overall survival compared to chemotherapy in the KEYNOTE-061 study. In this study, we aimed to explore the efficacy and safety of a three-drug regimen of PD-1 inhibitor combined with albumin paclitaxel and apatinib (a VEGFR inhibitor) for the second-line treatment of patients with metastatic gastric cancer (mGC).

Methods: This was a single-center, single-arm, phase II clinical study. Patients with mGC with stable microsatellite and negative HER-2 expression who failed first-line chemotherapy were enrolled. The enrolled patients were treated with PD-1 inhibitor (selected according to patients' requirements) in combination with albumin paclitaxel (125 mg/m2, intravenously, days 1 and 8, or 250 mg/m2, intravenously, day 1) and apatinib (250 or 500 mg, orally, days 1-21) every 3 weeks. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), duration of response, and adverse events (AEs).

Results: From July 11, 2019, to October 13, 2022, a total of 43 patients were enrolled, of whom 10 were PD-L1 negative, 11 were PD-L1 positive, and 22 had unknown PD-L1 expression. As of the data cutoff on April 1st, 2023, nine patients had partial response, 29 had stable disease, and five experienced progressive disease, with the ORR of 20.9% and DCR of 88.3%. The median PFS was 6.2 months (95% CI, 3.9-9.3), and the median OS was 10.1 months (95% CI, 7.5-14.1). All patients suffered from alopecia and neurotoxicity. The other main AEs of grade 1 or 2 were bone marrow suppression (N = 21, 48.8%), hand-foot reaction (N = 19, 44.2%), hypertension (N = 18, 41.9%), hypothyroidism (N = 11, 25.6%), gastrointestinal bleeding (N = 3, 7.0%), and liver function damage (N = 5, 11.6%). Two patients reported grade 3-4 immune-related liver damage.

Conclusion: Second-line PD-1 inhibitor combined with albumin paclitaxel and apatinib showed certain efficacy and safety in patients with mGC.

Trial registration: Clinical trials, NCT04182724. Registered 27 November 2019; retrospectively registered, https://clinicaltrials.gov/study/NCT04182724.

Abstract Image

PD-1抑制剂联合白蛋白紫杉醇和阿帕替尼作为转移性胃癌患者的二线治疗:一项单中心、单臂、II期研究。
背景:免疫检查点抑制剂已被批准用于晚期胃癌的一线和三线治疗:免疫检查点抑制剂已被批准用于晚期胃癌的一线和三线治疗。然而,在KEYNOTE-061研究中,与化疗相比,在二线治疗中单用pembrolizumab并不能改善总生存期。在这项研究中,我们旨在探讨PD-1抑制剂联合白蛋白紫杉醇和阿帕替尼(一种血管内皮生长因子抑制剂)三药方案二线治疗转移性胃癌(mGC)患者的有效性和安全性:这是一项单中心、单臂、II期临床研究。方法:这是一项单中心、单臂的II期临床研究,研究对象为微卫星稳定、HER-2表达阴性、一线化疗失败的转移性胃癌患者。入组患者接受PD-1抑制剂(根据患者需求选择)联合白蛋白紫杉醇(125毫克/平方米,静脉注射,第1天和第8天,或250毫克/平方米,静脉注射,第1天)和阿帕替尼(250或500毫克,口服,第1-21天)治疗,每3周一次。主要终点为无进展生存期(PFS),次要终点为总生存期(OS)、客观应答率(ORR)、疾病控制率(DCR)、应答持续时间和不良事件(AEs):2019年7月11日至2022年10月13日,共有43名患者入组,其中10人PD-L1阴性,11人PD-L1阳性,22人PD-L1表达未知。截至2023年4月1日数据截止时,9名患者有部分应答,29名患者病情稳定,5名患者病情进展,ORR为20.9%,DCR为88.3%。中位PFS为6.2个月(95% CI,3.9-9.3),中位OS为10.1个月(95% CI,7.5-14.1)。所有患者均出现脱发和神经毒性。其他1级或2级主要AE为骨髓抑制(21例,48.8%)、手足反应(19例,44.2%)、高血压(18例,41.9%)、甲状腺功能减退(11例,25.6%)、消化道出血(3例,7.0%)和肝功能损害(5例,11.6%)。两名患者报告了3-4级免疫相关肝损伤:结论:二线PD-1抑制剂联合白蛋白紫杉醇和阿帕替尼治疗mGC患者具有一定的疗效和安全性:临床试验,NCT04182724。注册时间:2019年11月27日;回顾性注册,https://clinicaltrials.gov/study/NCT04182724。
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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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