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用于治疗转移性黑色素瘤的新型免疫治疗药物和信号转导激酶小分子拮抗剂。

Novel immunotherapeutic agents and small molecule antagonists of signalling kinases for the treatment of metastatic melanoma.

机构信息

Division of Medical Oncology/Hematology, University of Louisville School of Medicine, James Graham Brown Cancer Center, KY 40202, USA.

出版信息

Drugs. 2011 Jul 9;71(10):1233-50. doi: 10.2165/11591380-000000000-00000.

Abstract

Melanoma incidence is increasing annually and over 40,000 die of this disease each year worldwide. In this review, we discuss the rationale and recent trial results of several novel immunotherapeutic approaches and small molecule inhibitors of signalling kinases. Ipilimumab is a humanized anti-CTLA4 antibody that has been proven to increase the median overall survival of large cohorts of patients with unresectable melanoma in two phase III trials. OncoVEX(GM-CSF) is an oncolytic herpes simplex virus-1 recombined with granulocyte-macrophage colony-stimulating factor that has demonstrated durable objective responses in a phase II trial. Tumour-infiltrating lymphocytes given after lymphocyte depletion and followed by high-dose interleukin (IL)-2 yield durable complete responses in a significant percentage of melanoma patients. Lastly, denileukin diftitox, a fusion of IL-2 and diphtheria toxin, was recently observed to deplete regulatory T cells and cause durable partial responses, particularly in chemo/immune-naïve patients. These agents are enabling the rational design of novel combination trials to simultaneously increase antigen presentation, deplete regulatory T cells and block immune check-points in order to activate melanoma antigen-specific immunity. Although melanoma metastases have been found to contain thousands of mutations, the V600E BRAF mutation is clearly a driver of the neoplastic phenotype and is present in 40-60% of melanomas. Two separate small molecule antagonists of B-Raf have been found to yield very high partial response rates in metastatic melanoma, and the B-Raf inhibitor, vemurafenib (PLX4032), was recently observed to increase median overall survival in an interim analysis. However, B-Raf inhibitor resistance through up-regulation or activating mutations of alternative oncogenic signalling receptors and enzymes is proving to be a major challenge. Inhibitors of c-Kit and mitogen-activated protein kinase (MEK) have also been found to have activity against melanomas and MEK inhibitors are now being examined as a strategy to overcome B-Raf inhibitor resistance. In summary, these studies reveal that, for the first time, several immunotherapeutic and targeted agents are yielding dramatic clinical responses and improvements in overall survival in patients with unresectable stage III and IV melanoma.

摘要

黑色素瘤的发病率每年都在增加,全球每年有超过 4 万人死于这种疾病。在这篇综述中,我们讨论了几种新型免疫治疗方法和信号激酶小分子抑制剂的基本原理和最近的试验结果。Ipilimumab 是一种人源化抗 CTLA-4 抗体,两项三期临床试验已经证明,它可以提高无法切除的黑色素瘤大队列患者的中位总生存期。OncoVEX(GM-CSF)是一种溶瘤单纯疱疹病毒 1 重组体,与粒细胞-巨噬细胞集落刺激因子结合,在一项二期试验中显示出持久的客观反应。在淋巴细胞耗竭后给予肿瘤浸润淋巴细胞,然后给予高剂量白细胞介素(IL)-2,可使黑色素瘤患者的很大一部分获得持久的完全缓解。最后,denileukin diftitox,一种 IL-2 和白喉毒素的融合物,最近被观察到可以耗尽调节性 T 细胞,并导致持久的部分缓解,特别是在化疗/免疫初治患者中。这些药物使合理设计新型联合试验成为可能,同时增加抗原呈递、耗尽调节性 T 细胞并阻断免疫检查点,以激活黑色素瘤抗原特异性免疫。尽管已经发现黑色素瘤转移灶含有数千种突变,但 V600E BRAF 突变显然是肿瘤表型的驱动因素,存在于 40-60%的黑色素瘤中。两种单独的 B-Raf 小分子拮抗剂已被发现对转移性黑色素瘤有很高的部分缓解率,B-Raf 抑制剂 vemurafenib(PLX4032)在中期分析中被观察到增加中位总生存期。然而,通过上调或激活替代致癌信号受体和酶的 B-Raf 抑制剂耐药性正成为一个主要挑战。c-Kit 和丝裂原活化蛋白激酶(MEK)抑制剂也被发现对黑色素瘤有活性,目前正在研究 MEK 抑制剂作为克服 B-Raf 抑制剂耐药性的策略。总之,这些研究表明,首次有几种免疫治疗和靶向药物在不可切除的 III 期和 IV 期黑色素瘤患者中产生了显著的临床反应和总生存期的改善。

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