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雷莫西尤单抗联合帕博利珠单抗用于初治晚期胃癌或胃食管交界腺癌:1a/b期JVDF试验的安全性和抗肿瘤活性

Ramucirumab in Combination with Pembrolizumab in Treatment-Naïve Advanced Gastric or GEJ Adenocarcinoma: Safety and Antitumor Activity from the Phase 1a/b JVDF Trial.

作者信息

Chau Ian, Penel Nicolas, Soriano Andres O, Arkenau Hendrik-Tobias, Cultrera Jennifer, Santana-Davila Rafael, Calvo Emiliano, Le Tourneau Christophe, Zender Lars, Bendell Johanna C, Mi Gu, Gao Ling, McNeely Samuel Clark, Oliveira Joana M, Ferry David, Herbst Roy S, Fuchs Charles S

机构信息

Gastrointestinal Units, Royal Marsden Hospital, London SM2 5PT, UK.

General Oncology Department, Medical Oncology Department, Oscar Lambret Cancer Center, 59020 Lille, France.

出版信息

Cancers (Basel). 2020 Oct 15;12(10):2985. doi: 10.3390/cancers12102985.

Abstract

Ramucirumab (anti-VEGFR2) plus pembrolizumab (anti-PD1) demonstrated promising antitumor activity and tolerability among patients with previously treated advanced cancers, supporting growing evidence that combination therapies modulating the tumor microenvironment may expand the spectrum of patients who respond to checkpoint inhibitors. Here we present the results of this combination in first-line patients with metastatic G/GEJ cancer. Twenty-eight patients (≥18 years) with no prior systemic chemotherapy in the advanced/metastatic setting received ramucirumab (8 mg/kg days 1 and 8) plus pembrolizumab (200 mg day 1) every 3 weeks as part of JVDF phase 1a/b study. The primary endpoint was safety. Secondary endpoints included progression-free survival (PFS), objective response rate (ORR), and overall survival (OS). Tumors were PD-L1-positive (combined positive score ≥ 1) in 19 and -negative in 6 patients. Eighteen patients experienced grade 3 treatment-related adverse events, most commonly hypertension (14%) and elevated alanine/aspartate aminotransferase (11% each), with no grade 4 or 5 reported. The ORR was 25% (PD-L1-positive, 32%; PD-L1-negative, 17%) with duration of response not reached. PFS was 5.6 months (PD-L1-positive, 8.6 months; PD-L1-negative, 4.3 months), and OS 14.6 months (PD-L1-positive, 17.3 months; PD-L1-negative, 11.3 months). Acknowledging study design limitations, ramucirumab plus pembrolizumab had encouraging durable clinical activity with no unexpected toxicities in treatment-naïve biomarker-unselected metastatic G/GEJ cancer, and improved outcomes in patients with PD-L1-positive tumors.

摘要

雷莫西尤单抗(抗血管内皮生长因子受体2)联合派姆单抗(抗程序性死亡蛋白1)在先前接受过治疗的晚期癌症患者中显示出了有前景的抗肿瘤活性和耐受性,这进一步证明了调节肿瘤微环境的联合疗法可能会扩大对检查点抑制剂有反应的患者范围。在此,我们展示了这种联合疗法用于一线转移性胃/胃食管交界腺癌患者的结果。作为JVDF 1a/b期研究的一部分,28例(≥18岁)在晚期/转移性疾病阶段未接受过全身化疗的患者每3周接受一次雷莫西尤单抗(第1天和第8天,8mg/kg)联合派姆单抗(第1天,200mg)治疗。主要终点是安全性。次要终点包括无进展生存期(PFS)、客观缓解率(ORR)和总生存期(OS)。19例患者的肿瘤为程序性死亡配体1阳性(联合阳性评分≥1),6例患者为阴性。18例患者发生了3级治疗相关不良事件,最常见的是高血压(14%)和丙氨酸/天冬氨酸转氨酶升高(各11%),未报告4级或5级不良事件。ORR为25%(程序性死亡配体1阳性患者为32%;程序性死亡配体1阴性患者为17%),缓解持续时间未达到。PFS为5.6个月(程序性死亡配体1阳性患者为8.6个月;程序性死亡配体1阴性患者为4.3个月),OS为14.6个月(程序性死亡配体1阳性患者为17.3个月;程序性死亡配体1阴性患者为11.3个月)。考虑到研究设计的局限性,雷莫西尤单抗联合派姆单抗在未经治疗、未选择生物标志物的转移性胃/胃食管交界腺癌中具有令人鼓舞的持久临床活性且无意外毒性,并且使程序性死亡配体1阳性肿瘤患者的预后得到改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a9/7602637/b4e2475b0e95/cancers-12-02985-g001.jpg

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