Blood. 2022 Dec 8;140(23):2514-2518. doi: 10.1182/blood.2022017960.
Lawal et al report on a 45-fold increase in secondary hematologic malignancy in 120 patients following hematopoietic stem cell transplantation (HSCT) for sickle cell disease (SCD), comparable to what has been reported following gene therapy. Notably, the cohort is enriched for older patients and for haploidentical transplant recipients with mixed chimerism following HSCT. These data further support the idea that pre-existing premalignant myeloid clones undergo clonal selection in the setting of nonmyeloablative HSCT and contribute to secondary malignancy.
Lawal 等人报告称,在 120 例因镰状细胞病(SCD)接受造血干细胞移植(HSCT)的患者中,继发性血液系统恶性肿瘤的发病率增加了 45 倍,与基因治疗后报告的情况相当。值得注意的是,该队列主要由老年患者和接受 HSCT 后嵌合状态为混合嵌合的单倍体异体移植受体组成。这些数据进一步支持了这样一种观点,即在非清髓性 HSCT 环境下,预先存在的恶性前髓细胞克隆经历克隆选择,并导致继发性恶性肿瘤。