Department of Hematology, Amsterdam UMC, University of Amsterdam, and LYMMCARE Amsterdam, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, The Netherlands.
Blood Adv. 2024 Jun 11;8(11):2740-2752. doi: 10.1182/bloodadvances.2023012145.
Several single-arm studies have explored the inclusion of brentuximab vedotin (BV) in salvage chemotherapy followed by autologous stem cell transplantation (ASCT) for relapsed/refractory (R/R) classical Hodgkin lymphoma (cHL). However, no head-to-head comparisons with standard salvage chemotherapy have been performed. This study presents a propensity score-matched analysis encompassing individual patient data from 10 clinical trials to evaluate the impact of BV in transplant-eligible patients with R/R cHL. We included 768 patients, of whom 386 were treated with BV with or without chemotherapy (BV cohort), whereas 382 received chemotherapy alone (chemotherapy cohort). Propensity score matching resulted in balanced cohorts of 240 patients each. No significant differences were observed in pre-ASCT complete metabolic response (CMR) rates (P = .69) or progression free survival (PFS; P = .14) between the BV and chemotherapy cohorts. However, in the BV vs chemotherapy cohort, patients with relapsed disease had a significantly better 3-year PFS of 80% vs 70%, respectively (P = .02), whereas there was no difference for patients with primary refractory disease (56% vs 62%, respectively; P = .67). Patients with stage IV disease achieved a significantly better 3-year PFS in the BV cohort (P = .015). Post-ASCT PFS was comparable for patients achieving a CMR after BV monotherapy and those receiving BV followed by sequential chemotherapy (P = .24). Although 3-year overall survival was higher in the BV cohort (92% vs 80%, respectively; P < .001), this is likely attributed to the use of other novel therapies in later lines for patients experiencing progression, given that studies in the BV cohort were conducted more recently. In conclusion, BV with or without salvage chemotherapy appears to enhance PFS in patients with relapsed disease but not in those with primary refractory cHL.
几项单臂研究探索了在挽救性化疗后加入 Brentuximab vedotin(BV)并进行自体干细胞移植(ASCT)治疗复发/难治性(R/R)经典霍奇金淋巴瘤(cHL)。然而,尚未与标准挽救性化疗进行头对头比较。本研究通过包含 10 项临床试验的个体患者数据进行了倾向评分匹配分析,以评估 BV 在适合移植的 R/R cHL 患者中的影响。我们纳入了 768 例患者,其中 386 例接受了 BV 联合或不联合化疗(BV 组)治疗,而 382 例仅接受了化疗(化疗组)。通过倾向评分匹配,两组各平衡了 240 例患者。在 ASCT 前完全代谢缓解(CMR)率(P=0.69)或无进展生存期(PFS;P=0.14)方面,BV 组和化疗组之间未观察到显著差异。然而,在 BV 与化疗组中,复发疾病患者的 3 年 PFS 分别为 80%和 70%,差异有统计学意义(P=0.02),而原发耐药疾病患者无差异(分别为 56%和 62%,P=0.67)。IV 期疾病患者在 BV 组中获得了显著更好的 3 年 PFS(P=0.015)。BV 单药治疗后达到 CMR 的患者和接受 BV 序贯化疗的患者的 ASCT 后 PFS 无差异(P=0.24)。尽管 BV 组的 3 年总生存率更高(分别为 92%和 80%,P<0.001),但这可能归因于在进展后患者使用了其他新型治疗方法,因为 BV 组中的研究是在最近进行的。总之,BV 联合或不联合挽救性化疗似乎可以提高复发疾病患者的 PFS,但不能提高原发耐药 cHL 患者的 PFS。