Instituto Nacional de Cancer, Bone Marrow Transplantation Department, Rio de Janeiro, Brazil.
Hospital Israelita Albert Einstein, Academic Research Organization, Guaramomis 480/64, São Paulo, 04076-010, Brazil.
Ann Hematol. 2024 Feb;103(2):603-607. doi: 10.1007/s00277-023-05532-8. Epub 2023 Nov 9.
Few studies have addressed the role of reduced-intensity conditioning (RIC) and non-myeloablative (NMA) regimens in older adults with Philadelphia acute lymphoblastic leukemia (Ph + ALL). The objective of this current study was to compare the outcomes of RIC/NMA versus TBI-based myeloablative (MAC) regimens in Ph + ALL patients older than 40 years old who underwent hematopoietic cell transplantation (HCT) in CR1. We used a freely available database from the CIBMTR. Transplants were performed between 2013 and 2017. With a median follow-up of 37.6 months, we have included 629 patients. We used propensity score weighting. Three-year OSs were 64% in the TBI-MAC group and 66% in the RIC/NMA group. OS was not different (HR = 0.92; p = 0.69). Three-year relapse incidences were 21.6% and 27.6% in the TBI-MAC and RIC/NMA groups. RIC/NMA was not associated with an increase in relapse rate (HR 1.02; p = 0.91). Three-year NRMs were 24.3% in the TBI-MAC group and 20.3% in the RIC/NMA group. RIC/NMA was not associated with superior NRM (HR 0.88; p = 0.57). In summary, we have shown that RIC/NMA regimens achieve outcomes comparable to TBI-based MAC in Ph+ ALL older patients in CR1 who may tolerate a TBI-based MAC regimen.
鲜有研究探讨减低强度预处理(RIC)和非清髓性(NMA)方案在老年费城染色体阳性急性淋巴细胞白血病(Ph+ ALL)患者中的作用。本研究旨在比较RIC/NMA 与基于全身照射(TBI)的清髓性(MAC)方案在初诊完全缓解(CR1)的老年 Ph+ ALL 患者行造血细胞移植(HCT)中的疗效。我们使用 CIBMTR 提供的一个免费数据库。移植于 2013 年至 2017 年期间进行。中位随访时间为 37.6 个月,共纳入 629 例患者。我们采用倾向评分加权法。TBI-MAC 组和 RIC/NMA 组的 3 年 OS 分别为 64%和 66%。两组 OS 无差异(HR=0.92,p=0.69)。TBI-MAC 组和 RIC/NMA 组的 3 年复发率分别为 21.6%和 27.6%。RIC/NMA 方案并未增加复发率(HR 1.02,p=0.91)。TBI-MAC 组和 RIC/NMA 组的 3 年非复发死亡率(NRM)分别为 24.3%和 20.3%。RIC/NMA 与 TBI-MAC 相比并未降低 NRM(HR 0.88,p=0.57)。综上所述,我们表明在初诊 CR1 的老年 Ph+ ALL 患者中,RIC/NMA 方案可取得与 TBI-MAC 方案相当的疗效,这些患者可能能够耐受 TBI-MAC 方案。