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本文引用的文献

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Safety Profile of Nivolumab Monotherapy: A Pooled Analysis of Patients With Advanced Melanoma.尼伏鲁单抗单药治疗的安全性概况:晚期黑色素瘤患者的汇总分析。
J Clin Oncol. 2017 Mar;35(7):785-792. doi: 10.1200/JCO.2015.66.1389. Epub 2016 Nov 14.
2
Anti-PD1 Pembrolizumab Can Induce Exceptional Fulminant Type 1 Diabetes.抗程序性死亡蛋白1(PD1)药物帕博利珠单抗可诱发罕见的暴发性1型糖尿病。
Diabetes Care. 2015 Nov;38(11):e182-3. doi: 10.2337/dc15-1331. Epub 2015 Aug 26.
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Risk of cutaneous toxicities in patients with solid tumors treated with immune checkpoint inhibitors: a meta-analysis.实体瘤患者接受免疫检查点抑制剂治疗时发生皮肤毒性的风险:一项荟萃分析。
Future Oncol. 2015;11(17):2471-84. doi: 10.2217/fon.15.118. Epub 2015 Aug 14.
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Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer.纳武单抗与多西他赛治疗晚期鳞状细胞非小细胞肺癌的疗效比较
N Engl J Med. 2015 Jul 9;373(2):123-35. doi: 10.1056/NEJMoa1504627. Epub 2015 May 31.
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PD-L1 protein expression in breast cancer is rare, enriched in basal-like tumours and associated with infiltrating lymphocytes.乳腺癌中 PD-L1 蛋白表达罕见,在基底样肿瘤中富集,并与浸润淋巴细胞相关。
Ann Oncol. 2015 Jul;26(7):1488-93. doi: 10.1093/annonc/mdv192. Epub 2015 Apr 20.
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Ipilimumab-induced toxicities and the gastroenterologist.伊匹单抗诱导的毒性与胃肠病学家
J Gastroenterol Hepatol. 2015 Apr;30(4):657-66. doi: 10.1111/jgh.12888.
7
Retinal vasculitis and ocular vitreous metastasis following complete response to PD-1 inhibition in a patient with metastatic cutaneous melanoma.患者转移性皮肤黑色素瘤经 PD-1 抑制治疗完全缓解后出现视网膜血管炎和眼玻璃体转移。
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Long-term follow-up of ipilimumab-induced hypophysitis, a common adverse event of the anti-CTLA-4 antibody in melanoma.Ipilimumab 诱导的垂体炎的长期随访,这是黑色素瘤抗 CTLA-4 抗体的常见不良事件。
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Bevacizumab plus ipilimumab in patients with metastatic melanoma.贝伐珠单抗联合伊匹单抗治疗转移性黑色素瘤患者。
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乳腺癌中的免疫检查点抑制剂——现状与未来方向

Checkpoint Inhibitors in Breast Cancer - Current Status and Future Directions.

作者信息

Bischoff Joachim

机构信息

Center for Clinical Trials, Städtisches Klinikum Dessau, Dessau, Germany.

出版信息

Breast Care (Basel). 2018 Mar;13(1):27-31. doi: 10.1159/000486706. Epub 2018 Feb 20.

DOI:10.1159/000486706
PMID:29950964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6016055/
Abstract

Antineoplastic agents directly targeting tumor cells have represented the major strategy of systemic anticancer therapy for many years. Nevertheless, overcoming resistance mechanisms remains a great challenge because treatment options are limited in many cases. From this point of view, immunotherapeutic approaches seem promising in a broad spectrum of solid tumors. These include in particular the currently available inhibitors directed against immune checkpoints leading to a significant T-cell activation. To date, the programmed death receptor 1 (PD-1) and its ligand are the most prominent targets in this context. However, the role of checkpoint inhibitors in the treatment of breast cancer is still being debated, and the main focus is on triple-negative breast cancer patients as a target population in many ongoing trials. Moreover, the potential superiority of combinations with other anticancer drugs such as cytotoxics and targeted agents will be discussed.

摘要

多年来,直接靶向肿瘤细胞的抗肿瘤药物一直是全身抗癌治疗的主要策略。然而,克服耐药机制仍然是一项巨大挑战,因为在许多情况下治疗选择有限。从这一角度来看,免疫治疗方法在多种实体瘤中似乎很有前景。这尤其包括目前可用的针对免疫检查点的抑制剂,这些抑制剂可导致显著的T细胞活化。迄今为止,程序性死亡受体1(PD-1)及其配体是这方面最突出的靶点。然而,检查点抑制剂在乳腺癌治疗中的作用仍在争论中,在许多正在进行的试验中,主要焦点是将三阴性乳腺癌患者作为目标人群。此外,还将讨论与其他抗癌药物(如细胞毒性药物和靶向药物)联合使用的潜在优势。