Department of Hematology, Anhui Provincial Hospital, the First Affiliated Hospital of USTC, Hefei, Anhui 230002.
Department of Hematology, Jiangsu Province Hospital and Nanjing Medical University First Affiliated Hospital, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Personalized Cancer Medicine, Nanjing Medical University, Nanjing, Jiangsu 210029.
Haematologica. 2023 Aug 1;108(8):2146-2154. doi: 10.3324/haematol.2022.282266.
Although classic Hodgkin lymphoma (cHL) is highly curable with current treatment paradigms, therapy fails in 10-25% of patients. This prospective multicenter phase II study attempted to investigate the efficacy and safety of the combination of tislelizumab with gemcitabine and oxaliplatin (T-GemOx) in relapsed or refractory cHL. Participants received six to eight courses of gemcitabine (1 g/m2 on day 1) and oxaliplatin (100 mg/m2 on day 1) combined with tislelizumab (200 mg on day 2) at 21-day intervals, followed by tislelizumab maintenance (every 2 months for 2 years). The main outcome measure was the best complete remission rate. As of August 2022, a total of 30 patients had been consecutively enrolled and given induction therapy. The best overall response rate and complete remission rate were 100% (95% confidence interval [CI]: 88.4-100%) and 96.7% (95% CI: 82.8-99.9%), respectively. The median duration of follow-up after initiation of T-GemOx was 15.8 months. The 12-month progression-free survival rate without autologous stem cell transplant was 96% (95% CI: 74.8-99.4%). There were 122 adverse events recorded, of which 93.4% were grade 1 or 2. Thrombocytopenia (10%) and anemia (6.7%) were the most common grade 3 or 4 adverse events. Overall, T-GemOx demonstrated promising antitumor activity with manageable toxicities as a salvage treatment for relapsed or refractory cHL. A longer follow-up duration is required to determine whether maintenance therapy with tislelizumab rather than transplantation can be curative following such a highly active regimen. This trial was registered with the Chinese Clinical Trials Registry (http://www.chictr.org.cn) on June 1, 2020, identifier ChiCTR2000033441.
尽管目前的治疗方案可使经典霍奇金淋巴瘤(cHL)的治愈率达到很高水平,但仍有 10-25%的患者治疗失败。本前瞻性多中心 II 期研究旨在探讨替雷利珠单抗联合吉西他滨和奥沙利铂(T-GemOx)在复发或难治性 cHL 患者中的疗效和安全性。参与者接受六个或八个疗程的吉西他滨(第 1 天 1 g/m2)和奥沙利铂(第 1 天 100 mg/m2)联合替雷利珠单抗(第 2 天 200 mg),每 21 天一次,随后进行替雷利珠单抗维持治疗(每 2 个月一次,持续 2 年)。主要终点为最佳完全缓解率。截至 2022 年 8 月,共有 30 例患者连续入组并接受诱导治疗。总体最佳缓解率和完全缓解率分别为 100%(95%可信区间[CI]:88.4-100%)和 96.7%(95%CI:82.8-99.9%)。T-GemOx 起始后中位随访时间为 15.8 个月。未进行自体干细胞移植的 12 个月无进展生存率为 96%(95%CI:74.8-99.4%)。记录到 122 例不良事件,其中 93.4%为 1 级或 2 级。血小板减少症(10%)和贫血症(6.7%)是最常见的 3 级或 4 级不良事件。总体而言,T-GemOx 作为复发或难治性 cHL 的挽救治疗方法,具有有前景的抗肿瘤活性和可管理的毒性。需要更长的随访时间来确定在如此高活性方案后,替雷利珠单抗维持治疗而非移植是否具有治愈作用。该试验于 2020 年 6 月 1 日在中国临床试验注册中心(http://www.chictr.org.cn)注册,注册号 ChiCTR2000033441。