Strocchio Luisa, Locatelli Franco
Department of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children's Hospital, Piazza S Onofrio, 4, Roma 00165, Italy.
Department of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children's Hospital, Piazza S Onofrio, 4, Roma 00165, Italy; Department of Pediatric Science, University of Pavia, Viale Brambilla 74, Pavia, Italy.
Hematol Oncol Clin North Am. 2018 Apr;32(2):317-328. doi: 10.1016/j.hoc.2017.11.011.
Although recent advances in gene therapy are expected to increase the chance of disease cure in thalassemia major, at present hematopoietic stem cell transplantation (HSCT) remains the only consolidated curative approach for this disorder. The widest experience has been obtained in the HLA-matched family donor (MFD) setting, with probabilities of overall and thalassemia-free survival exceeding 90% and 85%, respectively. As for most patients a suitable MFD is not available, alternative donors (HLA-matched unrelated donor, unrelated cord blood, HLA-haploidentical relative) have been increasingly explored, translating into the expansion of the number of patients treatable with HSCT.
尽管基因治疗的最新进展有望增加重型地中海贫血疾病治愈的机会,但目前造血干细胞移植(HSCT)仍然是这种疾病唯一经过验证的治愈方法。在人类白细胞抗原(HLA)匹配的家族供体(MFD)情况下积累了最广泛的经验,总体生存率和无地中海贫血生存率分别超过90%和85%。由于大多数患者没有合适的MFD,因此越来越多地探索替代供体(HLA匹配的无关供体、无关脐血、HLA单倍体相同的亲属),这使得可接受HSCT治疗的患者数量有所增加。