CTLA4 antagonists in phase I and phase II clinical trials, current status and future perspectives for cancer therapy

被引:21
|
作者
Szostak, Bartosz [1 ]
Machaj, Filip [1 ]
Rosik, Jakub [1 ]
Pawlik, Andrzej [1 ]
机构
[1] Pomeranian Med Univ, Dept Physiol, Szczecin, Poland
关键词
CTLA4; antagonists; cancer; therapy; checkpoint blockade; CTLA-4; inhibitors; ADVANCED MELANOMA; ADVERSE EVENTS; T-CELLS; RS231775; POLYMORPHISM; PREDICTING RESPONSE; REGULATORY T; OPEN-LABEL; IPILIMUMAB; NIVOLUMAB; SURVIVAL;
D O I
10.1080/13543784.2019.1559297
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In cancer, the immune response to tumor antigens is often suppressed by inhibitors and ligands. Checkpoint blockade, considered one of the most promising frontiers for anti-cancer therapy, aims to stimulate the immune anti-cancer response. Agents such as cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) inhibitors offer prolonged survival with manageable side effects.Areas covered: We summarize the recent clinical successes of CTLA-4 inhibitors and place a strong emphasis on those in early phase clinical trials, often in combination with other immune check-point inhibitors, i.e., programmed cell death protein 1 (PD-1) and BRAF/mitogen-activated protein kinase inhibitors.Expert opinion: Recent phase I and phase II clinical trials confirm the efficacy of anti-CTLA-4 therapy for treatment of cancers such as renal cell carcinoma. These studies also indicated increased efficacy with combined immune checkpoint blockade with PD-1 or Ras/Raf/mitogen-activated protein kinase/ERK kinase (MEK)/extracellular-signal-regulated kinase (ERK) inhibitors. Researchers must search for new immune targets that may enable more effective and safe immune checkpoint blockade and cancer therapy. This goal may be achieved by next-generation combination therapies to overcome immune checkpoint therapy resistance.
引用
收藏
页码:149 / 159
页数:11
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