Center for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Department of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Front Immunol. 2023 Jul 31;14:1229558. doi: 10.3389/fimmu.2023.1229558. eCollection 2023.
Classical Hodgkin lymphoma (cHL) is the most common pediatric lymphoma. Approximately 10% of patients develop refractory or recurrent disease. These patients are treated with intensive chemotherapy followed by consolidation with radiotherapy or high-dose chemotherapy and autologous stem cell reinfusion. Although this treatment is effective, it comes at the cost of severe long-term adverse events, such as reduced fertility and an increased risk of secondary cancers. Recently, promising results of inducing remission with the immune checkpoint inhibitor nivolumab (targeting PD-1) and the anti-CD30 antibody-drug conjugate Brentuximab vedotin (BV) +/- bendamustine were published.
Here we describe a cohort of 10 relapsed and refractory pediatric cHL patients treated with nivolumab + BV +/- bendamustine to induce remission prior to consolidation with standard treatment.
All patients achieved complete remission prior to consolidation treatment and are in ongoing complete remission with a median follow-up of 25 months (range: 12 to 42 months) after end-of-treatment. Only one adverse event of CTCAE grade 3 or higher due to nivolumab + BV was identified. Based on these results we conclude that immunotherapy with nivolumab + BV +/- bendamustine is an effective and safe treatment to induce remission in pediatric R/R cHL patients prior to standard consolidation treatment. We propose to evaluate this treatment further to study putative long-term toxicity and the possibility to reduce the intensity of consolidation treatment.
经典型霍奇金淋巴瘤(cHL)是最常见的儿科淋巴瘤。约有 10%的患者出现难治或复发。这些患者接受强化化疗,随后用放疗或大剂量化疗和自体干细胞回输进行巩固治疗。尽管这种治疗有效,但会带来严重的长期不良事件,如生育能力降低和二次癌症风险增加。最近,免疫检查点抑制剂nivolumab(针对 PD-1)和抗 CD30 抗体药物偶联物 Brentuximab vedotin(BV)+/-苯达莫司汀诱导缓解的结果令人鼓舞。
在这里,我们描述了一组 10 例复发/难治性儿科 cHL 患者,在接受标准治疗前用 nivolumab + BV +/-苯达莫司汀诱导缓解。
所有患者在巩固治疗前均达到完全缓解,在治疗结束后中位随访 25 个月(范围:12 至 42 个月)时持续完全缓解。仅发生 1 例因 nivolumab + BV 导致的 CTCAE 3 级或更高的不良事件。基于这些结果,我们得出结论,nivolumab + BV +/-苯达莫司汀免疫治疗可有效且安全地诱导儿科 R/R cHL 患者在标准巩固治疗前缓解。我们建议进一步评估这种治疗方法,以研究潜在的长期毒性和降低巩固治疗强度的可能性。