Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Blood Adv. 2023 Jul 11;7(13):3225-3231. doi: 10.1182/bloodadvances.2022009323.
Outcomes for children and adolescents with relapsed and refractory Hodgkin lymphoma (HL) are poor, with ∼50% of patients experiencing a subsequent relapse. The anti-CD30 antibody-drug conjugate brentuximab vedotin improved progression-free survival (PFS) when used as consolidation after autologous stem cell transplantation (ASCT) in adults with high-risk relapsed/refractory HL. Data on brentuximab vedotin as consolidative therapy after ASCT in pediatric patients with HL are extremely limited, with data of only 11 patients reported in the literature. We performed a retrospective analysis of 67 pediatric patients who received brentuximab vedotin as consolidation therapy after ASCT for the treatment of relapsed/refractory HL to describe the experience of this regimen in the pediatric population. This is the largest cohort reported to date. We found that brentuximab vedotin was well tolerated with a safety profile similar to that of adult patients. With a median follow-up of 37 months, the 3-year PFS was 85%. These data suggest a potential role for the use of brentuximab vedotin as consolidation therapy after ASCT for children with relapsed/refractory HL.
对于复发和难治性霍奇金淋巴瘤(HL)患儿和青少年患者,其预后较差,约有 50%的患者会随后复发。抗 CD30 抗体药物偶联物 Brentuximab vedotin 在接受自体干细胞移植(ASCT)后作为巩固治疗,可改善高危复发/难治性 HL 成人患者的无进展生存期(PFS)。在 HL 儿科患者中,ASCT 后使用 Brentuximab vedotin 作为巩固治疗的数据极其有限,文献中仅报道了 11 例患者的数据。我们对 67 例接受 Brentuximab vedotin 作为 ASCT 后巩固治疗复发/难治性 HL 的儿科患者进行了回顾性分析,以描述该方案在儿科人群中的应用经验。这是迄今为止报告的最大队列。我们发现 Brentuximab vedotin 具有良好的耐受性,其安全性与成人患者相似。中位随访 37 个月,3 年 PFS 为 85%。这些数据表明,Brentuximab vedotin 作为复发/难治性 HL 儿童 ASCT 后巩固治疗的一种潜在方法具有一定作用。