German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Department of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Eur J Haematol. 2022 Dec;109(6):728-735. doi: 10.1111/ejh.13859. Epub 2022 Oct 3.
Patients with classical Hodgkin lymphoma (cHL) relapsing after second-line therapy have a dismal prognosis and novel approaches are required for this patient group. Based on promising (pre-)clinical data and the favourable toxicity profile, we performed a phase II clinical trial with the JAK inhibitor ruxolitinib in patients with relapsed or refractory cHL (r/r cHL).
Patients ≥18 years with histologically confirmed r/r cHL who failed second-line treatment were included. Ruxolitinib was given orally at a dose of 25 mg twice daily in continuous 28-day cycles until progression or unacceptable toxicity. Primary endpoint was the PET/CT-based overall response rate (ORR; complete response (CR) or partial response (PR)) after 2 cycles; secondary endpoints included progression-free (PFS) and overall survival (OS) as well as feasibility. The Jericho Trial adopted a 2-stage phase 2 design (Simon 1989).
Among the 12 included patients in stage 1, 2 had a PR, 3 had a stable disease (SD) and 6 had progressive disease (PD) after two treatment cycles (ORR: 2/12 evaluable patients, 16.7%). Median PFS was 3.6 months, the 1-year OS estimate was 50.6% (median not reached). The toxicity profile was favourable with only one grade IV adverse event (7.1%) reported.
Ruxolitinib exhibited a favourable side effect profile but modest activity in r/r cHL. Although the formal stopping criterion after stage 1 was not met, the trial did not continue to stage 2 due to the low response and PFS rates observed in stage 1.
二线治疗后复发的经典霍奇金淋巴瘤(cHL)患者预后较差,需要为这一患者群体开发新的治疗方法。基于有前景的(临床前)数据和良好的毒性特征,我们在复发/难治性 cHL(r/r cHL)患者中开展了一项 II 期临床试验,评估 JAK 抑制剂芦可替尼的疗效。
纳入组织学证实的 r/r cHL 患者,这些患者二线治疗失败。芦可替尼口服,剂量为 25mg,每日 2 次,28 天为一个周期,持续给药,直至疾病进展或出现不可耐受的毒性。主要终点是 2 个周期后基于 PET/CT 的总缓解率(ORR;完全缓解(CR)或部分缓解(PR));次要终点包括无进展生存期(PFS)和总生存期(OS)以及可行性。Jericho 试验采用 Simon 1989 提出的两阶段 II 期设计。
在第 1 阶段的 12 例可评估患者中,2 例患者有部分缓解,3 例患者疾病稳定,6 例患者疾病进展(ORR:2/12 例可评估患者,16.7%)。中位 PFS 为 3.6 个月,1 年 OS 估计值为 50.6%(中位未达到)。毒性特征良好,仅报告 1 例 4 级不良事件(7.1%)。
芦可替尼在 r/r cHL 中具有良好的副作用特征和适度的疗效。尽管第 1 阶段后正式的停止标准未达到,但由于第 1 阶段观察到的缓解率和 PFS 率较低,试验未进入第 2 阶段。