Clinical research progress of targeted therapy combined with immunotherapy for advanced cholangiocarcinoma

被引:1
作者
Liu, Qin [1 ]
Chen, Yuanyuan [1 ]
Hu, Yan [1 ]
Yang, Jiyuan [1 ]
机构
[1] Yangtze Univ, Affiliated Hosp 1, Jingzhou, Peoples R China
关键词
Cholangiocarcinoma; Targeted therapy; Targeted therapy combined with; immunotherapy; BILIARY-TRACT CANCER; PHASE-II; SELECTIVE INHIBITOR; IN-VITRO; LENVATINIB; TORIPALIMAB; PATHWAYS; TUMORS; MEK;
D O I
10.1016/j.ctarc.2023.100771
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cholangiocarcinoma (CCA) is a common and highly malignant form of cancer that has shown high rates of morbidity and mortality in recent years. The prognosis for cholangiocarcinoma is generally poor due to its aggressive nature and high recurrence rate. Most patients are diagnosed in the middle or late stages of the disease, making surgical treatment challenging. As a result, there is a pressing need to improve the treatment of advanced cholangiocarcinoma. The advancement of tumor genetics has allowed for more precise and targeted treatment approaches. Targeted molecular therapy has shown promise in cholangiocarcinoma treatment, and the study of immunotherapy has provided hope for patients who are not eligible for surgery or have a poor response to chemotherapy. However, the effectiveness of single targeted therapy or immunotherapy is limited. Therefore, the combination of targeted therapy and immunotherapy represents a significant breakthrough and challenge. Recent research on the combination of targeted therapy and immunotherapy in cholangiocarcinoma has yielded promising results, surpassing the outcomes of single therapy or chemotherapy. This has sparked intense interest in further investigating this combined approach. In this article, we aim to review the development and research findings of targeted therapy combined with immunotherapy, providing new insights for the selection of combined therapy and future clinical research in cholangiocarcinoma.
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页数:9
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共 101 条
[41]   Genomic ERBB2/ERBB3 mutations promote PD-L1-mediated immune escape in gallbladder cancer: a whole-exome sequencing analysis [J].
Li, Maolan ;
Liu, Fatao ;
Zhang, Fei ;
Zhou, Weiping ;
Jiang, Xiaoqing ;
Yang, Yuan ;
Qu, Kai ;
Wang, Yueqi ;
Ma, Qiang ;
Wang, Ting ;
Bai, Lu ;
Wang, Zheng ;
Song, Xiaoling ;
Zhu, Yidi ;
Yuan, Ruiyan ;
Gao, Yuan ;
Liu, Yongchen ;
Jin, Yunpeng ;
Li, Huaifeng ;
Xiang, Shanshan ;
Ye, Yuanyuan ;
Zhang, Yijian ;
Jiang, Lin ;
Hu, Yunping ;
Hao, Yajuan ;
Lu, Wei ;
Chen, Shili ;
Gu, Jun ;
Zhou, Jian ;
Gong, Wei ;
Zhang, Yong ;
Wang, Xuefeng ;
Liu, Xiyong ;
Liu, Chang ;
Liu, Houbao ;
Liu, Yun ;
Liu, Yingbin .
GUT, 2019, 68 (06) :1024-1033
[42]   Long non-coding RNA MALAT1 promotes gastric cancer tumorigenicity and metastasis by regulating vasculogenic mimicry and angiogenesis [J].
Li, Yue ;
Wu, Zhenzhen ;
Yuan, Jia ;
Sun, Li ;
Lin, Li ;
Huang, Na ;
Bin, Jianping ;
Liao, Yulin ;
Liao, Wangjun .
CANCER LETTERS, 2017, 395 :31-44
[43]   Safety and efficacy of PD-1 blockade-activated multiple antigen-specific cellular therapy alone or in combination with apatinib in patients with advanced solid tumors: a pooled analysis of two prospective trials [J].
Liang, Lijun ;
Wen, Yixuan ;
Hu, Rong ;
Wang, Lei ;
Xia, Youyou ;
Hu, Chenxi ;
Qiao, Yun ;
Geng, Xiaowei ;
Chen, Ting ;
Fei, Jiayan ;
Hui, Kaiyuan ;
Jiang, Xiaodong .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2019, 68 (09) :1467-1477
[44]   Pembrolizumab combined with lenvatinib as non-first-line therapy in patients with refractory biliary tract carcinoma [J].
Lin, Jianzhen ;
Yang, Xu ;
Long, Junyu ;
Zhao, Songhui ;
Mao, Jinzhu ;
Wang, Dongxu ;
Bai, Yi ;
Bian, Jin ;
Zhang, Lei ;
Yang, Xiaobo ;
Wang, Anqiang ;
Xie, Fucun ;
Shi, Weiwei ;
Yang, Huayu ;
Pan, Jie ;
Hu, Ke ;
Guan, Mei ;
Zhao, Lin ;
Huo, Li ;
Mao, Yilei ;
Sang, Xinting ;
Wang, Kai ;
Zhao, Haitao .
HEPATOBILIARY SURGERY AND NUTRITION, 2020, 9 (04) :414-424
[45]   Immunotherapy in Biliary Tract Cancers: Current Standard-of-Care and Emerging Strategies [J].
Lo, Justin H. H. ;
Agarwal, Rajiv ;
Goff, Laura W. W. ;
Heumann, Thatcher R. R. .
CANCERS, 2023, 15 (13)
[46]   Updates in the use of targeted therapies for the treatment of cholangiocarcinoma [J].
Lodl, Emma ;
Ramnaraign, Brian ;
Sahin, Ilyas ;
Wheeler, Sarah .
JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2023, 29 (05) :1206-1217
[47]   RAS/MAPK Activation Is Associated with Reduced Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancer: Therapeutic Cooperation Between MEK and PD-1/PD-L1 Immune Checkpoint Inhibitors [J].
Loi, Sherene ;
Dushyanthen, Sathana ;
Beavis, Paul A. ;
Salgado, Roberto ;
Denkert, Carsten ;
Savas, Peter ;
Combs, Susan ;
Rimm, David L. ;
Giltnane, Jennifer M. ;
Estrada, Monica V. ;
Sanchez, Violeta ;
Sanders, Melinda E. ;
Cook, Rebecca S. ;
Pilkinton, Mark A. ;
Mallal, Simon A. ;
Wang, Kai ;
Miller, Vincent A. ;
Stephens, Phil J. ;
Yelensky, Roman ;
Doimi, Franco D. ;
Gomez, Henry ;
Ryzhov, Sergey V. ;
Darcy, Phillip K. ;
Arteaga, Carlos L. ;
Balko, Justin M. .
CLINICAL CANCER RESEARCH, 2016, 22 (06) :1499-1509
[48]   The safety concerns regarding immune checkpoint inhibitors in liver cancer patients rising mainly from CHB [J].
Lou, Shike ;
Cao, Zhujun ;
Chi, Wanqing ;
Wang, Xiaoyin ;
Feng, Mingyang ;
Lin, Lanyi ;
Ding, Yezhou ;
Liu, Kehui ;
Qu, Lihong ;
Zhao, Gangde ;
Bao, Shisan ;
Wang, Hui .
FRONTIERS IN PHARMACOLOGY, 2023, 14
[49]   LEAP-005: Phase II study of lenvatinib (len) plus pembrolizumab (pembro) in patients (pts) with previously treated advanced solid tumours [J].
Lwin, Z. ;
Gomez-Roca, C. ;
Saada-Bouzid, E. ;
Yanez, E. ;
Longo Munoz, F. ;
Im, S-A. ;
Castanon, E. ;
Senellart, H. ;
Graham, D. ;
Voss, M. ;
Doherty, M. ;
Lopez, J. ;
Ghori, R. ;
Kubiak, P. ;
Jin, F. ;
Norwood, K. ;
Chung, H. C. .
ANNALS OF ONCOLOGY, 2020, 31 :S1170-S1170
[50]  
Marabelle A, 2020, J CLIN ONCOL, V38, P1, DOI 10.1200/JCO.19.02105