Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Nat Med. 2020 Aug;26(8):1280-1284. doi: 10.1038/s41591-020-0918-0. Epub 2020 Jun 2.
An increasing fraction of patients with metastatic cancer develop leptomeningeal dissemination of disease (LMD), and survival is dismal. We conducted a single-arm, phase 2 study of pembrolizumab in patients with solid tumor malignancies and LMD (NCT02886585). Patients received 200 mg of pembrolizumab intravenously every 3 weeks until definitive progression or unacceptable toxicity. The primary endpoint was rate of overall survival at 3 months (OS3). Secondary objectives included toxicity, response rate and time to intracranial or extracranial disease progression. A Simon two-stage design was used to compare a null hypothesis OS3 of 18% against an alternative of 43%. Twenty patients-17 with breast cancer, two with lung cancer and one with ovarian cancer-were enrolled into the pre-specified evaluation group having received at least one dose of pembrolizumab. The median follow-up of surviving patients was 6.3 months (range, 2.2-12.5 months). The percentage of patients who experienced one (or more) grade 3 or higher adverse events at least possibly related to treatment was 40%, the most frequent being hyperglycemia (n = 6), nausea (n = 7) and vomiting (n = 7). The study met the primary endpoint, as 12 of 20 (OS3, 0.60; 90% confidence interval, 0.39-0.78) patients were alive at 3 months after enrollment. Pembrolizumab is safe and feasible and displays promising activity in patients with LMD. Further investigations are needed to identify which patients with LMD can benefit from pembrolizumab.
越来越多的转移性癌症患者出现脑膜疾病(LMD)的疾病扩散,且生存率较低。我们开展了一项单臂、2 期临床试验,评估派姆单抗在患有实体瘤恶性肿瘤和 LMD 的患者中的应用(NCT02886585)。患者接受 200mg 派姆单抗静脉输注,每 3 周一次,直到疾病进展或出现不可耐受的毒性。主要终点为 3 个月总生存率(OS3)。次要目标包括毒性、缓解率和颅内或颅外疾病进展时间。采用 Simon 两阶段设计,将 3 个月 OS3 的零假设(18%)与替代假设(43%)进行比较。20 名患者(17 名乳腺癌患者、2 名肺癌患者和 1 名卵巢癌患者)入组预设定评估组,至少接受了一剂派姆单抗治疗。生存患者的中位随访时间为 6.3 个月(范围 2.2-12.5 个月)。至少有 1 例(或更多)3 级或更高级别的不良事件发生且可能与治疗相关的患者比例为 40%,最常见的是高血糖(n=6)、恶心(n=7)和呕吐(n=7)。研究达到了主要终点,20 名患者中有 12 名(OS3,0.60;90%置信区间,0.39-0.78)在入组后 3 个月存活。派姆单抗安全可行,对 LMD 患者具有有前景的疗效。需要进一步的研究来确定哪些 LMD 患者可以从派姆单抗中获益。