Division of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Division of Biostatistics, City of Hope, Duarte, CA.
Blood. 2023 Oct 19;142(16):1359-1370. doi: 10.1182/blood.2023020485.
This phase 1 study evaluated the addition of vorinostat to pembrolizumab in patients with relapsed/refractory (RR) classical Hodgkin lymphoma (cHL), diffuse large B-cell lymphoma, and follicular lymphoma. We report the results in cases of cHL. Adult patients with RR cHL who had received ≥1 prior lines of therapy and were ineligible for transplantation were treated in a dose-escalation cohort with 2 dose levels (DLs) and then on an expansion cohort at the recommended phase 2 dose (RP2D) in 21-day cycles. Vorinostat 100 mg twice a day (DL1) and 200 mg twice a day (DL2) was administered orally from days 1 to 5 and 8 to 12; all patients received pembrolizumab 200 mg IV every 3 weeks. The primary end point was safety and determination of RP2D. In total, 32 patients with cHL were enrolled, including 30 at DL2 (RP2D); 78% had received prior anti-programmed cell death 1 (anti-PD-1) therapy, and 56% were PD-1 refractory. Grade ≥3 adverse events (AEs) included hypertension (9%), neutropenia (9%), hypophosphatemia (9%), thrombocytopenia (6%), and lymphopenia (6%). Immune-related AEs included grade 1 or 2 thyroiditis (13%), grade 1 rash (6%), and grade 3 esophagitis/duodenitis (3%). The overall response rate (ORR) was 72% and complete response (CR) rate was 34%. Patients refractory to prior PD-1 blockade (n = 18) had ORR and CR rates of 56% and 11%, respectively. Pembrolizumab and vorinostat was well tolerated with a high ORR rate in RR cHL including in anti-PD-1-refractory disease. This trial was registered at www.clinicaltrials.gov as #NCT03150329.
这项 1 期研究评估了沃里诺他汀联合帕博利珠单抗治疗复发/难治性(RR)经典霍奇金淋巴瘤(cHL)、弥漫性大 B 细胞淋巴瘤和滤泡性淋巴瘤患者的效果。我们报告了 cHL 的结果。接受过≥1 线治疗且不符合移植条件的 RR cHL 成年患者在剂量递增队列中接受 2 个剂量水平(DL)治疗,然后在 21 天周期的推荐 2 期剂量(RP2D)扩展队列中接受治疗。DL1 组患者口服沃里诺他汀 100mg,每日 2 次;DL2 组患者口服沃里诺他汀 200mg,每日 2 次,从第 1 天至第 5 天和第 8 天至第 12 天给药;所有患者均接受帕博利珠单抗 200mg,静脉输注,每 3 周 1 次。主要终点是安全性和确定 RP2D。共纳入 32 例 cHL 患者,其中 30 例在 DL2(RP2D);78%的患者曾接受过抗程序性死亡 1(抗 PD-1)治疗,56%的患者对 PD-1 治疗耐药。≥3 级不良事件(AE)包括高血压(9%)、中性粒细胞减少症(9%)、低磷血症(9%)、血小板减少症(6%)和淋巴细胞减少症(6%)。免疫相关 AE 包括 1 级或 2 级甲状腺炎(13%)、1 级皮疹(6%)和 3 级食管炎/十二指肠炎(3%)。总缓解率(ORR)为 72%,完全缓解率(CR)为 34%。先前对 PD-1 阻断剂耐药的患者(n=18)的 ORR 和 CR 率分别为 56%和 11%。帕博利珠单抗联合沃里诺他汀在 RR cHL 患者中具有良好的耐受性,ORR 率较高,包括对 PD-1 耐药的疾病。该试验在 www.clinicaltrials.gov 注册,编号为 #NCT03150329。