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

被引:0
|
作者
Zhu, Yu-Chun [1 ]
Wei, Zhi-Gong [2 ,3 ]
Wang, Jing-Jing [2 ,3 ]
Pei, Yi-Yan [2 ,3 ]
Jin, Jing [2 ,3 ]
Li, Dong [4 ]
Li, Zhi-Hui [4 ]
Liu, Zhe-Ran [2 ,3 ]
Min, Yu [2 ,3 ]
Li, Rui-Dan [2 ,3 ]
Yang, Li [2 ,3 ]
Liu, Ji-Yan [2 ,3 ]
Wei, Qiang [1 ]
Peng, Xing-Chen [2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Urol, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Canc Ctr, Dept Biotherapy, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
[4] Gen Hosp Western Theater Command, Dept Oncol, Chengdu, Peoples R China
关键词
2-STAGE DESIGNS; OPEN-LABEL; IMMUNOTHERAPY; MITOTANE;
D O I
10.1038/s41467-024-54661-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. Immune checkpoint inhibitors have shown some activity in patients with adrenocortical carcinoma (ACC), a rare aggressive malignancy with limited treatment options. Here the authors report the results of a phase 2 trial of camrelizumab (anti-PD1) plus apatinib (VEGFR inhibitor) for previously treated ACC.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Camrelizumab monotherapy or plus apatinib for PD-L1-positive advanced pulmonary sarcomatoid carcinoma: A single-arm, open-label, multicenter, phase II study
    Zhao, M.
    Liu, X.
    Yuan, C.
    Zheng, W.
    Zhang, D.
    Long, Q.
    Li, J.
    Han, T.
    Xu, L.
    Li, H.
    Li, X.
    Shi, S.
    ANNALS OF ONCOLOGY, 2022, 33 : S36 - S37
  • [32] Neoadjuvant camrelizumab plus chemotherapy in patients with locally advanced cervical cancer (NACI): A prospective, single-arm, phase II trial
    Chen, J.
    Li, K.
    Han, Y.
    Shen, Y.
    Wang, Y.
    Song, K.
    Chen, X.
    Xia, B.
    Zou, D.
    Wang, Y.
    Ma, D.
    ANNALS OF ONCOLOGY, 2022, 33 (07) : S804 - S804
  • [33] Neoadjuvant camrelizumab plus chemotherapy for locally advanced cervical cancer (NACI study): A prospective, single-arm, phase II trial
    Chen, Jing
    Li, Kezhen
    Hu, Yingjie
    Han, Yingyan
    Shen, Yuanming
    Wang, Yanzhou
    Song, Kun
    Xia, Bairong
    Chen, Xiaojun
    Zou, Dongling
    Wang, Yingmei
    Sun, Chaoyang
    Chen, Gang
    Ma, Ding
    JOURNAL OF CLINICAL ONCOLOGY, 2023, 41 (16)
  • [34] Camrelizumab plus apatinib successfully treated a patient with advanced esophageal squamous cell carcinoma
    Yan, Zheng
    Yao, Zhi-Hua
    Yao, Shu-Na
    Wang, Hai-Ying
    Chu, Jun-Feng
    Song, Ming
    Zhao, Shuang
    Liu, Yan-Yan
    IMMUNOTHERAPY, 2020, 12 (16) : 1161 - 1166
  • [35] Camrelizumab combined with EP/EC chemotherapy followed by camrelizumab plus apatinib for first-line therapy of advanced extrapulmonary neuroendocrine carcinoma: A prospective, single-arm, multicenter clinical study
    Dai, Y.
    Hong, Q.
    ANNALS OF ONCOLOGY, 2023, 34 : S710 - S710
  • [36] Camrelizumab in combination with apatinib as a perioperative treatment for patients with hepatocellular carcinoma at high risk of recurrence: A prospective, single-arm, phase 2 study
    Cui, Yunlong
    Bao, Xu
    Yu, Ge
    Li, Huikai
    Fang, Feng
    Li, Qiang
    Zhang, Wei
    Wu, Qiang
    Chen, Lu
    Liu, Chen
    Song, Tianqiang
    JOURNAL OF CLINICAL ONCOLOGY, 2023, 41 (16)
  • [37] Apatinib in patients with advanced chordoma: a single-arm, single-centre, phase 2 study
    Liu, Chao
    Jia, Qi
    Wei, Haifeng
    Yang, Xinghai
    Liu, Tielong
    Zhao, Jian
    Ling, Yan
    Wang, Chenguang
    Yu, Hongyu
    Li, Zhenxi
    Jiao, Jian
    Wu, Zhipeng
    Yang, Cheng
    Xiao, Jianru
    LANCET ONCOLOGY, 2020, 21 (09): : 1244 - 1252
  • [38] Camrelizumab plus apatinib after progression on immune checkpoint inhibitors in patients with advanced esophageal squamous cell carcinoma (CAP 02 Re-challenge): A single-arm multicenter, phase II trial.
    Meng, Xiangrui
    Wang, Junsheng
    Xia, Jin
    Wu, Tao
    Luo, Zhiquan
    Hong, Yong-Gui
    Lu, Ping
    Guo, Yanzhen
    Ji, Yinghua
    Zhang, Min
    Yang, Liuzhong
    Cheng, Peng
    Liang, Wenchang
    Shan, Zhengzheng
    Fan, Qingxia
    Wang, Feng
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (3_SUPPL) : 364 - 364
  • [39] Camrelizumab plus apatinib combined with POF in patients with untreated advanced gastric cancer (UAGC): A singlecenter, open-label, single-arm, phase II trial (SYLT-017)
    Su, L.
    Zhao, S.
    Lin, P.
    Yin, Y.
    Lin, R.
    ANNALS OF ONCOLOGY, 2022, 33 (07) : S1119 - S1120
  • [40] Camrelizumab plus apatinib in patients with advanced or recurrent endometrial cancer after failure of at least first-line therapy: Interim results of a single-arm phase II trial.
    Wang, Huaying
    Tian, Wenjuan
    Ren, Yulan
    Jing, Chuyu
    Shan, Boer
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (16)