Lee Jung-Min, Cimino-Mathews Ashley, Peer Cody J, Zimmer Alexandra, Lipkowitz Stanley, Annunziata Christina M, Cao Liang, Harrell Maria I, Swisher Elizabeth M, Houston Nicole, Botesteanu Dana-Adriana, Taube Janis M, Thompson Elizabeth, Ogurtsova Aleksandra, Xu Haiying, Nguyen Jeffers, Ho Tony W, Figg William D, Kohn Elise C
Jung-Min Lee, Cody J. Peer, Alexandra Zimmer, Stanley Lipkowitz, Christina M. Annunziata, Liang Cao, Nicole Houston, Dana-Adriana Botesteanu, Jeffers Nguyen, William D. Figg, and Elise C. Kohn, Center for Cancer Research, National Cancer Institute, Bethesda; Ashley Cimino-Mathews, Janis M. Taube, Elizabeth Thompson, Aleksandra Ogurtsova, and Haiying Xu, The Johns Hopkins Medical Institution, Baltimore; and Tony W. Ho, AstraZeneca, Gaithersburg, MD; and Maria I. Harrell and Elizabeth M. Swisher, University of Washington, Seattle, WA.
J Clin Oncol. 2017 Jul 1;35(19):2193-2202. doi: 10.1200/JCO.2016.72.1340. Epub 2017 May 4.
Purpose Data suggest that DNA damage by poly (ADP-ribose) polymerase inhibition and/or reduced vascular endothelial growth factor signaling by vascular endothelial growth factor receptor inhibition may complement antitumor activity of immune checkpoint blockade. We hypothesize the programmed death-ligand 1 (PD-L1) inhibitor, durvalumab, olaparib, or cediranib combinations are tolerable and active in recurrent women's cancers. Patients and Methods This phase I study tested durvalumab doublets in parallel 3 + 3 dose escalations. Durvalumab was administered at 10 mg/kg every 2 weeks or 1,500 mg every 4 weeks with either olaparib tablets twice daily or cediranib on two schedules. The primary end point was the recommended phase II dose (RP2D). Response rate and pharmacokinetic analysis were secondary end points. Results Between June 2015 and May 2016, 26 women were enrolled. The RP2D was durvalumab 1,500 mg every 4 weeks with olaparib 300 mg twice a day, or cediranib 20 mg, 5 days on/2 days off. No dose-limiting toxicity was recorded with durvalumab plus olaparib. The cediranib intermittent schedule (n = 6) was examined because of recurrent grade 2 and non-dose-limiting toxicity grade 3 and 4 adverse events (AEs) on the daily schedule (n = 8). Treatment-emergent AEs included hypertension (two of eight), diarrhea (two of eight), pulmonary embolism (two of eight), pulmonary hypertension (one of eight), and lymphopenia (one of eight). Durvalumab plus intermittent cediranib grade 3 and 4 AEs were hypertension (one of six) and fatigue (one of six). Exposure to durvalumab increased cediranib area under the curve and maximum plasma concentration on the daily, but not intermittent, schedules. Two partial responses (≥15 months and ≥ 11 months) and eight stable diseases ≥ 4 months (median, 8 months [4 to 14.5 months]) were seen in patients who received durvalumab plus olaparib, yielding an 83% disease control rate. Six partial responses (≥ 5 to ≥ 8 months) and three stable diseases ≥ 4 months (4 to ≥ 8 months) were seen in 12 evaluable patients who received durvalumab plus cediranib, for a 50% response rate and a 75% disease control rate. Response to therapy was independent of PD-L1 expression. Conclusion To our knowledge, this is the first reported anti-PD-L1 plus olaparib or cediranib combination therapy. The RP2Ds of durvalumab plus olaparib and durvalumab plus intermittent cediranib are tolerable and active. Phase II studies with biomarker evaluation are ongoing.
目的 数据表明,聚(ADP - 核糖)聚合酶抑制导致的DNA损伤和/或血管内皮生长因子受体抑制引起的血管内皮生长因子信号传导减少可能补充免疫检查点阻断的抗肿瘤活性。我们假设程序性死亡配体1(PD - L1)抑制剂度伐利尤单抗、奥拉帕利或西地尼布联合用药在复发性妇科癌症中耐受性良好且具有活性。患者与方法 这项I期研究采用平行的3 + 3剂量递增试验测试度伐利尤单抗联合用药方案。度伐利尤单抗每2周以10 mg/kg给药或每4周以1500 mg给药,同时联合每日两次口服奥拉帕利片或两种给药方案的西地尼布。主要终点是推荐的II期剂量(RP2D)。缓解率和药代动力学分析为次要终点。结果 在2015年6月至2016年5月期间,纳入了26名女性患者。RP2D为度伐利尤单抗每4周1500 mg联合奥拉帕利每日300 mg两次,或西地尼布20 mg,给药5天/停药2天。度伐利尤单抗联合奥拉帕利未记录到剂量限制性毒性。由于每日给药方案(n = 8)出现复发性2级以及非剂量限制性毒性3级和4级不良事件(AE),对西地尼布间歇给药方案(n = 6)进行了研究。治疗中出现的AE包括高血压(8例中的2例)、腹泻(8例中的2例)、肺栓塞(8例中的2例)、肺动脉高压(8例中的1例)和淋巴细胞减少(8例中的1例)。度伐利尤单抗联合间歇给药西地尼布的3级和4级AE为高血压(6例中的1例)和疲劳(6例中的1例)。每日给药方案下,度伐利尤单抗的暴露增加了西地尼布的曲线下面积和最大血浆浓度,但间歇给药方案下未增加。接受度伐利尤单抗联合奥拉帕利治疗的患者中观察到2例部分缓解(分别≥15个月和≥11个月)以及8例疾病稳定≥4个月(中位数8个月[4至14.5个月]),疾病控制率为83%。在12例可评估的接受度伐利尤单抗联合西地尼布治疗的患者中观察到6例部分缓解(≥5至≥8个月)和3例疾病稳定≥4个月(4至≥8个月),缓解率为50%,疾病控制率为75%。治疗反应与PD - L1表达无关。结论 据我们所知,这是首次报道的抗PD - L1联合奥拉帕利或西地尼布的联合治疗。度伐利尤单抗联合奥拉帕利和度伐利尤单抗联合间歇给药西地尼布的RP2D耐受性良好且具有活性。正在进行有生物标志物评估的II期研究。