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癌症治疗中的免疫检查点阻断疗法

Immune Checkpoint Blockade in Cancer Therapy.

作者信息

Postow Michael A, Callahan Margaret K, Wolchok Jedd D

机构信息

All authors: Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY.

出版信息

J Clin Oncol. 2015 Jun 10;33(17):1974-82. doi: 10.1200/JCO.2014.59.4358. Epub 2015 Jan 20.


DOI:10.1200/JCO.2014.59.4358
PMID:25605845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4980573/
Abstract

Immunologic checkpoint blockade with antibodies that target cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and the programmed cell death protein 1 pathway (PD-1/PD-L1) have demonstrated promise in a variety of malignancies. Ipilimumab (CTLA-4) and pembrolizumab (PD-1) are approved by the US Food and Drug Administration for the treatment of advanced melanoma, and additional regulatory approvals are expected across the oncologic spectrum for a variety of other agents that target these pathways. Treatment with both CTLA-4 and PD-1/PD-L1 blockade is associated with a unique pattern of adverse events called immune-related adverse events, and occasionally, unusual kinetics of tumor response are seen. Combination approaches involving CTLA-4 and PD-1/PD-L1 blockade are being investigated to determine whether they enhance the efficacy of either approach alone. Principles learned during the development of CTLA-4 and PD-1/PD-L1 approaches will likely be used as new immunologic checkpoint blocking antibodies begin clinical investigation.

摘要

使用靶向细胞毒性T淋巴细胞相关抗原4(CTLA-4)和程序性细胞死亡蛋白1通路(PD-1/PD-L1)的抗体进行免疫检查点阻断,已在多种恶性肿瘤中显示出前景。伊匹单抗(CTLA-4)和帕博利珠单抗(PD-1)已获美国食品药品监督管理局批准用于治疗晚期黑色素瘤,预计针对这些通路的多种其他药物在整个肿瘤学领域也将获得更多监管批准。同时使用CTLA-4和PD-1/PD-L1阻断治疗会出现一种独特的不良事件模式,称为免疫相关不良事件,偶尔还会出现不寻常的肿瘤反应动力学。目前正在研究涉及CTLA-4和PD-1/PD-L1阻断的联合治疗方法,以确定它们是否能增强单独使用任一方法的疗效。随着新型免疫检查点阻断抗体开始临床研究,在CTLA-4和PD-1/PD-L1治疗方法研发过程中所学到的原则可能会被应用。

相似文献

[1]
Immune Checkpoint Blockade in Cancer Therapy.

J Clin Oncol. 2015-6-10

[2]
The Next Immune-Checkpoint Inhibitors: PD-1/PD-L1 Blockade in Melanoma.

Clin Ther. 2015-4-1

[3]
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J Chin Med Assoc. 2017-1

[4]
Managing immune checkpoint-blocking antibody side effects.

Am Soc Clin Oncol Educ Book. 2015

[5]
Prognostic factors and outcomes in metastatic uveal melanoma treated with programmed cell death-1 or combined PD-1/cytotoxic T-lymphocyte antigen-4 inhibition.

Eur J Cancer. 2017-9

[6]
The evolution of checkpoint blockade as a cancer therapy: what's here, what's next?

Curr Opin Immunol. 2015-1-23

[7]
CTLA-4 and PD-1/PD-L1 blockade: new immunotherapeutic modalities with durable clinical benefit in melanoma patients.

Clin Cancer Res. 2013-10-1

[8]
PD-1 checkpoint blockade alone or combined PD-1 and CTLA-4 blockade as immunotherapy for lung cancer?

Expert Opin Biol Ther. 2017-3

[9]
Checkpoint blocking antibodies in cancer immunotherapy.

FEBS Lett. 2013-10-23

[10]
Immune checkpoint blockade: a common denominator approach to cancer therapy.

Cancer Cell. 2015-4-13

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本文引用的文献

[1]
Genetic basis for clinical response to CTLA-4 blockade in melanoma.

N Engl J Med. 2014-12-4

[2]
Ipilimumab in patients with melanoma and autoimmune disease.

J Immunother Cancer. 2014-10-14

[3]
Severe relapse in a multiple sclerosis patient associated with ipilimumab treatment of melanoma.

Mult Scler. 2015-4

[4]
Successful treatment with Ipilimumab and Interleukin-2 in two patients with metastatic melanoma and systemic autoimmune disease.

Cancer Immunol Immunother. 2014-12

[5]
Abscopal effects of radiotherapy on advanced melanoma patients who progressed after ipilimumab immunotherapy.

Oncoimmunology. 2014-5-14

[6]
Anti-programmed-death-receptor-1 treatment with pembrolizumab in ipilimumab-refractory advanced melanoma: a randomised dose-comparison cohort of a phase 1 trial.

Lancet. 2014-7-15

[7]
Opportunistic infections in patients treated with immunotherapy for cancer.

J Immunother Cancer. 2014-6-18

[8]
Combining targeted therapy with immunotherapy in BRAF-mutant melanoma: promise and challenges.

J Clin Oncol. 2014-7-20

[9]
Ipilimumab versus placebo after radiotherapy in patients with metastatic castration-resistant prostate cancer that had progressed after docetaxel chemotherapy (CA184-043): a multicentre, randomised, double-blind, phase 3 trial.

Lancet Oncol. 2014-5-13

[10]
Effects of MAPK and PI3K pathways on PD-L1 expression in melanoma.

Clin Cancer Res. 2014-7-1

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