Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Department of Hematology, Imamura General Hospital, Kagoshima, Japan.
Ann Hematol. 2021 Jan;100(1):197-208. doi: 10.1007/s00277-020-04310-0. Epub 2020 Nov 5.
Retransplantation is the only curative treatment option for patients with acute lymphoblastic leukemia (ALL) that has relapsed after allogeneic hematopoietic cell transplantation (allo-HCT); however, data in this setting remain scant. Hence, this multicenter, retrospective study aims to determine outcome predictors after retransplantation in relapsed ALL. We examined 55 recipients who underwent multiple allo-HCTs during 2006-2018. The 2-year overall survival (OS), progression-free survival (PFS), and non-relapse mortality rates were 35.9%, 29.1%, and 23.6%, respectively. We observed a trend of better outcome in Ph + ALL (n = 22) patients compared with non-Ph ALL (n = 33) patients; the 2-year PFS was 40.9% versus 21.2%, indicating a beneficial effect of more potent second- or third-generation tyrosine kinase inhibitors. Univariate analysis revealed that late relapse after the previous transplant was the only significant predictor of better transplant outcome among Ph + ALL patients, whereas factors related to prolonged OS/PFS in non-Ph ALL patients were late relapse after the previous transplant, longer duration from disease relapse/progression to second or more allo-HCT, disease status at the transplantation, and good performance status. Nevertheless, further investigations are warranted to determine whether novel molecular-targeted agents with higher efficacy and fewer toxicities could exceed conventional chemotherapies as a bridging strategy to next allo-HCT and improve the outcomes of non-Ph ALL patients.
中文译文:
同种异体造血细胞移植(allo-HCT)后复发的急性淋巴细胞白血病(ALL)患者,唯一的治愈性治疗选择是再次移植;然而,该领域的数据仍然有限。因此,这项多中心、回顾性研究旨在确定复发 ALL 患者再次移植后的预后预测因素。我们研究了 55 名在 2006 年至 2018 年间接受多次 allo-HCT 的患者。2 年总生存率(OS)、无进展生存率(PFS)和非复发死亡率分别为 35.9%、29.1%和 23.6%。我们观察到 Ph+ALL(n=22)患者的结局优于非 Ph ALL(n=33)患者,有改善趋势;2 年 PFS 分别为 40.9%和 21.2%,表明更有效的第二代或第三代酪氨酸激酶抑制剂有获益作用。单因素分析显示,在前一次移植后晚期复发是 Ph+ALL 患者移植结局更好的唯一显著预测因素,而非 Ph ALL 患者与延长 OS/PFS 相关的因素是在前一次移植后晚期复发、从疾病复发/进展到第二次或更多次 allo-HCT 的时间较长、移植时疾病状态和良好的体能状态。然而,仍需要进一步研究,以确定是否有更高疗效和更少毒性的新型分子靶向药物可以超越传统化疗,作为桥接策略到下一次 allo-HCT,并改善非 Ph ALL 患者的结局。