Time to abandon CAR-T monotherapy for solid tumors

被引:9
|
作者
Yin, Limei [1 ,2 ,3 ]
Wan, Zhengwei [1 ,2 ,3 ]
Sun, Ping [1 ,2 ,3 ]
Shuai, Ping [1 ,2 ,3 ]
Liu, Yuping [1 ,2 ,3 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Hlth Management, Chengdu, Peoples R China
[2] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Inst Hlth Management, Chengdu, Peoples R China
[3] Chinese Acad Sci, Sichuan Translat Med Res Hosp, Chengdu, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2023年 / 1878卷 / 04期
关键词
Solid tumor; Immunotherapy; Combined therapy; PHASE-I; ANTITUMOR EFFICACY; ONCOLYTIC VIRUSES; BREAST-CANCER; CHECKPOINT BLOCKADE; CELL THERAPY; IMMUNOTHERAPY; GROWTH; HER2; LYMPHODEPLETION;
D O I
10.1016/j.bbcan.2023.188930
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent decades, chimeric antigen receptor T (CAR-T) cell therapy has achieved dramatic success in patients with hematological malignancies. However, CAR-T cell therapy failed to effectively treat solid tumors as a monotherapy. By summarizing the challenges of CAR-T cell monotherapy for solid tumors and analyzing the underlying mechanisms of combinatorial strategies to counteract these hurdles, we found that complementary therapeutics are needed to improve the scant and transient responses of CAR-T cell monotherapy in solid tumors. Further data, especially data from multicenter clinical trials regarding efficacy, toxicity, and predictive biomarkers are required before the CAR-T combination therapy can be translated into clinical settings.
引用
收藏
页数:10
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