González-Cao M, Arance A, Piulats J M, Marquez-Rodas I, Manzano J L, Berrocal A, Crespo G, Rodriguez D, Perez-Ruiz E, Berciano M, Soria A, Castano A G, Espinosa E, Montagut C, Alonso L, Puertolas T, Aguado C, Royo M A, Blanco R, Rodríguez J F, Muñoz E, Mut P, Barron F, Martin-Algarra S
Translational Cancer Research Unit, Dr. Rosell Oncology Institute, Quiron Dexeus University Hospital, 08028, Barcelona, Spain.
Hospital Clinic I Provincial, Barcelona, Spain.
Clin Transl Oncol. 2017 Jun;19(6):761-768. doi: 10.1007/s12094-016-1602-1. Epub 2017 Jan 4.
The programmed death (PD-1) inhibitor pembrolizumab has been recently approved for the treatment of advanced melanoma. We evaluated the clinical activity of pembrolizumab in melanoma patients treated under the Spanish Expanded Access Program.
Advanced melanoma patients who failed to previous treatment lines were treated with pembrolizumab 2 mg/kg every three weeks. Patients with brain metastases were not excluded if they were asymptomatic. Data were retrospectively collected from 21 centers in the Spanish Melanoma Group.
Sixty-seven advanced melanoma patients were analyzed. Most patients were stage M1c (73.1%), had high LDH levels (55.2%) and had ECOG PS 1 or higher (59.7%). For cutaneous melanoma patients, median overall survival was 14.0 months; the 18-month overall survival rate was 47.1%. Overall response rate was 27%, including three patients with complete responses (6.5%). Median response duration was not reached, with 83.3% of responses ongoing (3.5 m+ to 20.4 m+). From ten patients included with brain metastases, four (40%) had an objective response, two (20%) of them achieved a complete response. Significant prognostic factors for overall survival were LDH level, ECOG PS and objective response. There were no serious adverse events.
Although this was a heavily pretreated cohort, pembrolizumab activity at the approved dose and schedule was confirmed in the clinical setting with long-term responders, also including patients with brain metastases.
程序性死亡(PD-1)抑制剂帕博利珠单抗最近已被批准用于治疗晚期黑色素瘤。我们评估了帕博利珠单抗在西班牙扩大使用计划下治疗的黑色素瘤患者中的临床活性。
既往治疗线失败的晚期黑色素瘤患者接受每三周一次2mg/kg帕博利珠单抗治疗。脑转移患者如果无症状则不被排除。数据从西班牙黑色素瘤研究组的21个中心进行回顾性收集。
分析了67例晚期黑色素瘤患者。大多数患者为M1c期(73.1%),乳酸脱氢酶(LDH)水平高(55.2%),东部肿瘤协作组(ECOG)体能状态评分为PS 1或更高(59.7%)。对于皮肤黑色素瘤患者,中位总生存期为14.0个月;18个月总生存率为47.1%。总缓解率为27%,包括3例完全缓解患者(6.5%)。中位缓解持续时间未达到,83.3%的缓解仍在持续(3.5个月至20.4个月以上)。纳入的10例脑转移患者中,4例(40%)有客观缓解,其中2例(20%)达到完全缓解。总生存期的显著预后因素为LDH水平、ECOG PS和客观缓解。无严重不良事件。
尽管这是一个接受过大量预处理的队列,但在临床环境中,帕博利珠单抗在批准的剂量和给药方案下的活性在长期缓解者中得到证实,也包括脑转移患者。