Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Lancet Oncol. 2018 Mar;19(3):347-355. doi: 10.1016/S1470-2045(18)30062-7. Epub 2018 Jan 26.
Treatment options are limited for patients with thymic carcinoma. These aggressive tumours are not typically associated with paraneoplastic autoimmune disorders, and strong PD-L1 expression has been reported in thymic epithelial tumours. We aimed to assess the activity of pembrolizumab, a monoclonal antibody that targets PD-1, in patients with advanced thymic carcinoma.
We completed a single-arm phase 2 study of pembrolizumab in patients with recurrent thymic carcinoma who had progressed after at least one line of chemotherapy. This was a single-centre study performed at Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Key inclusion criteria were an Eastern Cooperative Oncology Group performance status of 0-2, no history of autoimmune disease or other malignancy requiring treatment or laboratory abnormality, and adequate organ function. Patients received 200 mg of pembrolizumab every 3 weeks for up to 2 years. The primary objective of the study was the proportion of patients who had achieved a response assessed with Response Evaluation Criteria in Solid Tumors version 1.1. Analysis was per protocol, in all eligible patients. The study is registered with ClinicalTrials.gov, number NCT02364076, and is closed to accrual; we report the final analysis.
41 patients were enrolled from March 12, 2015, to Dec 16, 2016, of whom 40 were eligible and evaluable and one was excluded because of elevated liver enzymes at screening. The median follow-up was 20 months (IQR 14-26). The proportion of patients who achieved a response was 22·5% (95% CI 10·8-38·5); one (3%) patient achieved a complete response, eight (20%) patients achieved partial responses, and 21 (53%) patients achieved stable disease. The most common grade 3 or 4 adverse events were increased aspartate aminotransferase and alanine aminotransferase (five [13%] patients each). Six (15%) patients developed severe autoimmune toxicity, including two (5%) patients with myocarditis. There were 17 deaths at the time of analysis, but no deaths due to toxicity.
Pembrolizumab is a promising treatment option in patients with thymic carcinoma. Because severe autoimmune disorders are more frequent in thymic carcinoma than in other tumour types, careful monitoring is essential.
Merck & Co.
胸腺癌患者的治疗选择有限。这些侵袭性肿瘤通常与副肿瘤自身免疫性疾病无关,并且在胸上皮性肿瘤中已报道有强烈的 PD-L1 表达。我们旨在评估 pembrolizumab(一种靶向 PD-1 的单克隆抗体)在晚期胸腺癌患者中的活性。
我们在 Lombardi 综合癌症中心(美国华盛顿特区乔治敦大学)进行了一项 pembrolizumab 治疗复发的胸腺癌患者的单臂 2 期研究,这些患者在至少一线化疗后进展。这是一项单中心研究,纳入标准为东部合作肿瘤学组(ECOG)体能状态为 0-2,无自身免疫性疾病或其他需要治疗的恶性肿瘤史或其他实验室异常,以及足够的器官功能。患者每 3 周接受 200mg pembrolizumab,最长 2 年。研究的主要目的是根据实体瘤反应评估标准 1.1 评估的缓解患者比例。分析是按方案进行的,适用于所有合格患者。该研究在 ClinicalTrials.gov 注册,编号为 NCT02364076,目前已关闭入组,我们报告最终分析结果。
2015 年 3 月 12 日至 2016 年 12 月 16 日期间共纳入 41 例患者,其中 40 例符合入组和评估标准,1 例因筛选时肝酶升高而被排除。中位随访时间为 20 个月(IQR 14-26)。缓解患者比例为 22.5%(95%CI 10.8-38.5);1 例(3%)患者达到完全缓解,8 例(20%)患者达到部分缓解,21 例(53%)患者达到稳定疾病。最常见的 3 级或 4 级不良事件为天门冬氨酸氨基转移酶和丙氨酸氨基转移酶升高(各 5 例[13%])。6 例(15%)患者发生严重自身免疫毒性,包括 2 例(5%)心肌炎患者。分析时共 17 例死亡,但无因毒性导致的死亡。
pembrolizumab 是胸腺癌患者有前途的治疗选择。由于胸腺癌比其他肿瘤类型更常发生严重的自身免疫性疾病,因此需要密切监测。
默克公司。