Texas Children's Cancer Center, Texas Children's Hospital, Houston, Texas, USA.
Department of Pediatrics, Division of Pediatric Hematology and Oncology, Baylor College of Medicine, Houston, Texas, USA.
Br J Haematol. 2024 May;204(5):1888-1893. doi: 10.1111/bjh.19376. Epub 2024 Mar 19.
Over 50% of patients with systemic LCH are not cured with front-line therapies, and data to guide salvage options are limited. We describe 58 patients with LCH who were treated with clofarabine. Clofarabine monotherapy was active against LCH in this cohort, including heavily pretreated patients with a systemic objective response rate of 92.6%, higher in children (93.8%) than adults (83.3%). BRAF variant allele frequency in peripheral blood is correlated with clinical responses. Prospective multicentre trials are warranted to determine optimal dosing, long-term efficacy, late toxicities, relative cost and patient-reported outcomes of clofarabine compared to alternative LCH salvage therapy strategies.
超过 50%的全身性 LCH 患者无法通过一线治疗治愈,且可供指导挽救治疗选择的数据有限。我们描述了 58 例接受克拉屈滨治疗的 LCH 患者。在该队列中,克拉屈滨单药治疗对 LCH 具有活性,包括接受过多线治疗的患者,全身客观缓解率为 92.6%,儿童(93.8%)高于成人(83.3%)。外周血 BRAF 变异等位基因频率与临床反应相关。需要开展前瞻性多中心试验,以确定与其他 LCH 挽救治疗策略相比,克拉屈滨的最佳剂量、长期疗效、迟发性毒性、相对成本和患者报告结局。