Molecular-targeted agents combination therapy for cancer: Developments and potentials

被引:110
|
作者
Li, Feifei [1 ,2 ,3 ]
Zhao, Changqi [1 ,2 ]
Wang, Lili [3 ]
机构
[1] Beijing Normal Univ, Minist Educ, Key Lab Cell Proliferat & Regulat Biol, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, Gene Engn & Biotechnol Beijing Key Lab, Beijing 100875, Peoples R China
[3] Acad Mil Med Sci, Inst Pharmacol & Toxicol, Beijing 100850, Peoples R China
关键词
relapse; anticancer efficacy; chemotherapy; molecular-targeted agents; combination therapy; signaling pathway; CELL LUNG-CANCER; METASTATIC BREAST-CANCER; PHASE-III TRIAL; GROWTH-FACTOR RECEPTOR; ADVANCED PANCREATIC-CANCER; TYROSINE KINASE INHIBITOR; 1ST-LINE TREATMENT; DOUBLE-BLIND; MEK INHIBITION; RAPAMYCIN INHIBITOR;
D O I
10.1002/ijc.28261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although chemotherapy has advanced into the era of targeted drugs, the antitumor efficacies of current therapies are limited, most likely because of the high degree of cancer clonal heterogeneity, intratumor genetic heterogeneity and cell signal complexity. As shutdown of a single target does not necessarily eradicate the cancer, the use of combinations of molecular-targeted agents (MATs) has been proposed, and some pioneering research has been conducted to examine the efficacy of this strategy. In this article, the clinical and preclinical studies that are underway in an attempt to improve the anticancer efficacy of chemotherapies through combination strategies are summarized. Studies of combining cytotoxic agents with MATs, coinhibiting two or more targets in a single pathway or coinhibiting parallel or compensatory pathways as well as specific combinations will be introduced, and the antitumor potentials of each combination strategy will be evaluated.
引用
收藏
页码:1257 / 1269
页数:13
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