Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital, Blå stråket 2, 413 45, Gothenburg, Sweden.
Department of Surgery, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital, Blå stråket 5, 413 45, Gothenburg, Sweden.
BMC Cancer. 2019 May 2;19(1):415. doi: 10.1186/s12885-019-5623-3.
While recent years have seen a revolution in the treatment of metastatic cutaneous melanoma, no treatment has yet been able to demonstrate any prolonged survival in metastatic uveal melanoma. Thus, metastatic uveal melanoma remains a disease with an urgent unmet medical need. Reports of treatment with immune checkpoint inhibitors have thus far been disappointing. Based on animal experiments, it is reasonable to hypothesize that the effect of immunotherapy may be augmented by epigenetic therapy. Proposed mechanisms include enhanced expression of HLA class I and cancer antigens on cancer cells, as well as suppression of myeloid suppressor cells.
The PEMDAC study is a multicenter, open label phase II study assessing the efficacy of concomitant use of the PD1 inhibitor pembrolizumab and the class I HDAC inhibitor entinostat in adult patients with metastatic uveal melanoma. Primary endpoint is objective response rate. Eligible patients have histologically confirmed metastatic uveal melanoma, ECOG performance status 0-1, measurable disease as per RECIST 1.1 and may have received any number of prior therapies, with the exception of anticancer immunotherapy. Twenty nine patients will be enrolled. Patients receive pembrolizumab 200 mg intravenously every third week in combination with entinostat 5 mg orally once weekly. Treatment will continue until progression of disease or intolerable toxicity or for a maximum of 24 months.
The PEMDAC study is the first trial to assess whether the addition of an HDAC inhibitor to anti-PD1 therapy can yield objective anti-tumoral responses in metastatic UM.
ClinicalTrials.gov registration number: NCT02697630 . (Registered 3 March 2016). EudraCT registration number: 2016-002114-50.
近年来,转移性皮肤黑色素瘤的治疗取得了革命性进展,但尚无任何治疗方法能够延长转移性葡萄膜黑色素瘤患者的生存时间。因此,转移性葡萄膜黑色素瘤仍然是一种存在迫切未满足医疗需求的疾病。免疫检查点抑制剂治疗的报告迄今为止令人失望。基于动物实验,有理由假设表观遗传学治疗可能增强免疫治疗的效果。提出的机制包括增强癌细胞上 HLA Ⅰ类和癌症抗原的表达,以及抑制髓样抑制细胞。
PEMDAC 研究是一项多中心、开放标签的 II 期研究,评估 PD1 抑制剂 pembrolizumab 和 I 类 HDAC 抑制剂 entinostat 联合用于转移性葡萄膜黑色素瘤成人患者的疗效。主要终点是客观缓解率。符合条件的患者具有组织学证实的转移性葡萄膜黑色素瘤、ECOG 表现状态 0-1、根据 RECIST 1.1 可测量的疾病,并且可以接受任何数量的既往治疗,除了抗癌免疫疗法。将招募 29 名患者。患者每 3 周接受 200mg 静脉注射 pembrolizumab 联合每周一次口服 5mg entinostat。治疗将持续到疾病进展或无法耐受毒性或最长 24 个月。
PEMDAC 研究是评估 HDAC 抑制剂联合抗 PD1 治疗是否能在转移性 UM 中产生客观抗肿瘤反应的首次试验。
ClinicalTrials.gov 注册号:NCT02697630。(2016 年 3 月 3 日注册)。EudraCT 注册号:2016-002114-50。