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卡瑞利珠单抗联合阿帕替尼治疗既往治疗的晚期肾上腺皮质癌:一项单臂、2 期临床试验。

Camrelizumab plus apatinib for previously treated advanced adrenocortical carcinoma: a single-arm phase 2 trial.

机构信息

Department of Urology, West China Hospital, Sichuan University, Chengdu, China.

Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Nat Commun. 2024 Nov 29;15(1):10371. doi: 10.1038/s41467-024-54661-9.

Abstract

Adrenocortical carcinoma (ACC) is a rare, aggressive malignancy with a poor prognosis. Therapeutic options for patients with advanced ACC who have failed standard treatments are limited. Single-agent immunotherapy as a second-line treatment has shown unsatisfactory clinical outcomes. This phase II trial (NCT04318730) evaluated the efficacy and safety of the PD-1 inhibitor camrelizumab combined with the VEGFR inhibitor apatinib in previously treated advanced ACC. The primary endpoint was objective response rate (ORR). The secondary endpoints included progression-free survival (PFS), overall survival (OS), and safety. A total of 21 patients with advanced ACC received at least one dose of camrelizumab and apatinib. The ORR was 52% (95% CI, 30-74%), meeting the primary endpoint, and the disease control rate (DCR) was 95% (95% CI, 76-100%). The median PFS was 13.3 months (95% CI, 8.4-NE), and the median OS was 20.9 months (95% CI, 11.0-NE). The most common grade 3-4 treatment-related adverse events were alanine aminotransferase elevation, aspartate aminotransferase elevation, and lymphopenia. Predefined exploratory analyses indicated that patients with higher peripheral blood CXCR3 + CD8 + T cell abundance, lower immunosuppressive CD4 + T cell abundance, and higher overlap of clonotypes between tumor-infiltrating T cells and circulating T cells, were more likely to respond favorably to the combined therapy.

摘要

肾上腺皮质癌 (ACC) 是一种罕见的、侵袭性强的恶性肿瘤,预后较差。对于标准治疗失败的晚期 ACC 患者,治疗选择有限。作为二线治疗的单一药物免疫疗法的临床疗效并不令人满意。这项 II 期临床试验(NCT04318730)评估了 PD-1 抑制剂卡瑞利珠单抗联合血管内皮生长因子受体抑制剂阿帕替尼治疗既往治疗后晚期 ACC 的疗效和安全性。主要终点是客观缓解率(ORR)。次要终点包括无进展生存期(PFS)、总生存期(OS)和安全性。共有 21 名晚期 ACC 患者接受了至少一剂卡瑞利珠单抗和阿帕替尼治疗。ORR 为 52%(95%CI,30-74%),达到了主要终点,疾病控制率(DCR)为 95%(95%CI,76-100%)。中位 PFS 为 13.3 个月(95%CI,8.4-NE),中位 OS 为 20.9 个月(95%CI,11.0-NE)。最常见的 3-4 级治疗相关不良事件是丙氨酸氨基转移酶升高、天冬氨酸氨基转移酶升高和淋巴细胞减少。预先设定的探索性分析表明,外周血中 CXCR3+CD8+T 细胞丰度较高、免疫抑制性 CD4+T 细胞丰度较低、肿瘤浸润性 T 细胞和循环 T 细胞之间的克隆型重叠较高的患者,更有可能对联合治疗有良好的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cac/11604670/3d22c5e3f73a/41467_2024_54661_Fig1_HTML.jpg

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