Kottschade Lisa A, McWilliams Robert R, Markovic Svetomir N, Block Matthew S, Villasboas Bisneto Jose, Pham Anthony Q, Esplin Brandt L, Dronca Roxana S
Departments of aOncology bHematology cImmunology, Mayo Clinic, Rochester, Minnesota, USA.
Melanoma Res. 2016 Jun;26(3):300-3. doi: 10.1097/CMR.0000000000000242.
Uveal melanoma is a rare type of melanoma, with only five to seven cases per one million persons diagnosed each year. Patients with metastatic melanoma of uveal origin tend to have lower response rates on traditional therapies. Herein we report our experience with 10 patients with metastatic uveal melanoma (MUM) who received pembrolizumab. Eligible patients were more than or equal to 18 years old, had unresectable MUM, progressed on prior ipilimumab therapy, had good performance status (Eastern Cooperative Oncology Group of 0 or 1), and adequate organ and marrow function. Patients could have central nervous system disease, but needed to be clinically stable. Patients were treated with 2 mg/kg pembrolizumab intravenously over 30 min every 3 weeks until disease progression, unacceptable toxicity, or for up to 2 years. Between April 2014 and October 2014, we treated a total of 10 patients with MUM with pembrolizumab. Median age was 65 years, with 70% being female. As of the data cutoff date of 14 May 2015, median progression-free survival was 18 weeks (range 3.14-49.3 weeks), with four patients still currently receiving therapy. Of eight evaluable patients, there was one complete response, two partial responses, and one patient with stable disease. Four patients had rapidly progressive disease. Toxicities were as expected and were usually grade 1/2 in nature. Although this cohort of patients was small, to our knowledge this is the first such report of outcomes in uveal melanoma patients being treated with anti-PD1 therapy. In the absence of a clinical trial, treatment with pembrolizumab appears to be a viable option for patients with MUM.
葡萄膜黑色素瘤是一种罕见的黑色素瘤类型,每年每百万人口中仅有5至7例被诊断出来。葡萄膜来源的转移性黑色素瘤患者对传统疗法的反应率往往较低。在此,我们报告了10例接受派姆单抗治疗的转移性葡萄膜黑色素瘤(MUM)患者的治疗经验。符合条件的患者年龄大于或等于18岁,患有不可切除的MUM,先前接受伊匹单抗治疗后病情进展,体能状态良好(东部肿瘤协作组0或1级),且器官和骨髓功能正常。患者可能患有中枢神经系统疾病,但需要临床稳定。患者每3周静脉注射2mg/kg派姆单抗,持续30分钟,直至疾病进展、出现不可接受的毒性反应或长达2年。在2014年4月至2014年10月期间,我们共对10例MUM患者使用派姆单抗进行了治疗。中位年龄为65岁,70%为女性。截至2015年5月14日的数据截止日期,中位无进展生存期为18周(范围为3.14 - 49.3周),有4例患者目前仍在接受治疗。在8例可评估的患者中,有1例完全缓解,2例部分缓解,1例病情稳定。4例患者疾病迅速进展。毒性反应如预期,通常为1/2级。尽管该患者队列规模较小,但据我们所知,这是首例关于使用抗PD - 1疗法治疗葡萄膜黑色素瘤患者疗效的此类报告。在缺乏临床试验的情况下,对于MUM患者,使用派姆单抗治疗似乎是一种可行的选择。