Bender Carolin, Enk Alexander, Gutzmer Ralf, Hassel Jessica C
Department of Dermatology and National Center for Tumor Diseases, University Hospital Heidelberg, Im Neuenheimer Feld 440/460, Heidelberg, 69120, Germany.
Department of Dermatology and Allergy, Skin Cancer Center Hannover, Hannover Medical School, Ricklinger Str. 5, Hannover, 30449, Germany.
Cancer Med. 2017 Jul;6(7):1581-1586. doi: 10.1002/cam4.887. Epub 2017 Jun 21.
Uveal melanomas (UMs) are a rare form of cancer with clinical and pathological characteristics distinct from cutaneous melanomas. Ipilimumab has shown efficacy and safety in the treatment of metastatic UM. This provides a rationale for treatment with other immune checkpoint inhibitors. This is a retrospective review of 15 patients with metastatic UM treated between June 2014 and February 2016, who received treatment with the anti-PD-1 Abs pembrolizumab or nivolumab. Patients were treated at two German university hospitals. Therapy was administered at the approved dosing schedules of 2 mg/kg q3w for pembrolizumab and 3 mg/kg q2w for nivolumab. Treatment was given until first tumor assessment and continued if tumor assessment showed disease control. Tumor assessments were performed at baseline and following scans every 12 weeks. Patients were monitored throughout for adverse events. Best response to treatment was stable disease in four patients. Eight out of 15 (53%) patients received treatment until first tumor assessment. As of February 2016, median progression-free survival (PFS) is 3 months (range 0.75-6.75 months) and overall survival (OS) is 5 months (range 1-16 months). Eight out of 15 (53%) patients are still alive (two patients lost to follow-up) with one out of four patients is in ongoing disease control. Patients with multiple organ metastases and elevated serum lactate dehydrogenase did not respond well to treatment. No objective response to PD-1 Ab therapy was seen. Best response to treatment was stable disease in four patients. Treatment was well tolerated with manageable toxicity.
葡萄膜黑色素瘤(UMs)是一种罕见的癌症形式,其临床和病理特征与皮肤黑色素瘤不同。伊匹单抗已显示出在转移性UM治疗中的疗效和安全性。这为使用其他免疫检查点抑制剂进行治疗提供了理论依据。这是一项对2014年6月至2016年2月期间接受治疗的15例转移性UM患者的回顾性研究,这些患者接受了抗PD-1抗体帕博利珠单抗或纳武利尤单抗治疗。患者在两家德国大学医院接受治疗。治疗按照帕博利珠单抗2mg/kg每3周一次和纳武利尤单抗3mg/kg每2周一次的批准给药方案进行。治疗持续到首次肿瘤评估,如果肿瘤评估显示疾病得到控制则继续治疗。在基线时以及每12周扫描后进行肿瘤评估。在整个治疗过程中对患者进行不良事件监测。对治疗的最佳反应是4例患者病情稳定。15例患者中有8例(53%)接受治疗直至首次肿瘤评估。截至2016年2月,中位无进展生存期(PFS)为3个月(范围0.75 - 6.75个月),总生存期(OS)为5个月(范围1 - 16个月)。15例患者中有8例(53%)仍然存活(2例患者失访),4例患者中有1例疾病仍处于控制中。有多个器官转移且血清乳酸脱氢酶升高的患者对治疗反应不佳。未观察到对PD-1抗体治疗的客观反应。对治疗的最佳反应是4例患者病情稳定。治疗耐受性良好,毒性可控。