Emory University Winship Cancer Institute, Atlanta, GA.
Department of Radiology and.
Blood. 2021 Mar 11;137(10):1318-1326. doi: 10.1182/blood.2020007400.
Pembrolizumab, a humanized IgG4 monoclonal antibody targeting programmed death-1 protein, has demonstrated efficacy in relapsed/refractory classical Hodgkin lymphoma (cHL). To assess the complete metabolic response (CMR) rate and safety of pembrolizumab monotherapy in newly diagnosed cHL, we conducted a multicenter, single-arm, phase 2 investigator-initiated trial of sequential pembrolizumab and doxorubicin, vinblastine, and dacarbazine (AVD) chemotherapy. Patients ≥18 years of age with untreated, early, unfavorable, or advanced-stage disease were eligible for treatment. Thirty patients (early unfavorable stage, n = 12; advanced stage, n = 18) were treated with 3 cycles of pembrolizumab monotherapy followed by AVD for 4 to 6 cycles, depending on stage and bulk. Twelve had either large mediastinal masses or bulky disease (>10 cm). After pembrolizumab monotherapy, 11 patients (37%) demonstrated CMRs, and an additional 7 of 28 (25%) patients with quantifiable positron emission tomography computed tomography scans had >90% reduction in metabolic tumor volume. All patients achieved CMR after 2 cycles of AVD and maintained their responses at the end of treatment. With a median follow-up of 22.5 months (range, 14.2-30.6) there were no changes in therapy, progressions, or deaths. No patients received consolidation radiotherapy, including those with bulky disease. Therapy was well tolerated. The most common immune-related adverse events were grade 1 rash (n = 6) and grade 2 infusion reactions (n = 4). One patient had reversible grade 4 transaminitis and a second had reversible Bell's palsy. Brief pembrolizumab monotherapy followed by AVD was both highly effective and safe in patients with newly diagnosed cHL, including those with bulky disease. This trial was registered at www.clinicaltrials.gov as #NCT03226249.
派姆单抗是一种针对程序性死亡-1 蛋白的人源化 IgG4 单克隆抗体,已被证明在复发/难治性经典霍奇金淋巴瘤(cHL)中有效。为了评估派姆单抗单药治疗新诊断的 cHL 的完全代谢缓解(CMR)率和安全性,我们开展了一项多中心、单臂、研究者发起的 2 期临床试验,在该试验中,患者接受序贯派姆单抗和多柔比星、长春新碱和达卡巴嗪(AVD)化疗。适合治疗的患者为未经治疗、早期、不良或晚期疾病且年龄≥18 岁。30 例患者(早期不良预后 12 例,晚期 18 例)接受 3 个周期的派姆单抗单药治疗,然后根据分期和肿块大小接受 4-6 个周期的 AVD 化疗。12 例患者有大纵隔肿块或大肿块(>10cm)。派姆单抗单药治疗后,11 例(37%)患者达到 CMR,28 例可定量正电子发射断层扫描计算机断层扫描患者中,有 7 例(25%)患者的代谢肿瘤体积减少了>90%。所有患者在 AVD 治疗 2 个周期后均达到 CMR,并在治疗结束时维持缓解。中位随访时间为 22.5 个月(范围 14.2-30.6),没有改变治疗方案、进展或死亡。没有患者接受巩固性放疗,包括大肿块患者。治疗耐受性良好。最常见的免疫相关不良事件为 1 级皮疹(n=6)和 2 级输液反应(n=4)。1 例患者出现可逆性 4 级转氨酶升高,另 1 例患者出现可逆性贝尔氏面瘫。新诊断的 cHL 患者,包括大肿块患者,接受短暂的派姆单抗单药治疗后序贯 AVD 治疗,疗效高且安全性好。该试验在 www.clinicaltrials.gov 注册,编号为 #NCT03226249。