Zeidner Joshua F, Zahurak Marianna, Rosner Gary L, Gocke Christopher D, Jones Richard J, Smith B Douglas
Division of Hematologic Malignancies, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine , Baltimore, MD , USA.
Leuk Lymphoma. 2015 Jan;56(1):128-34. doi: 10.3109/10428194.2014.910868. Epub 2014 Jun 16.
The optimal treatment for chronic myeloid leukemia (CML) relapsing following allogeneic bone marrow transplant (alloBMT) is unknown. We performed a single-center retrospective analysis of 71 consecutive patients undergoing alloBMT for CML from 1995 to 2008. A multi-state model was used to quantify cumulative incidences of complete molecular response (CMR) and death following alloBMT. The primary analysis was comparison of three treatment interventions (tyrosine kinase inhibitor: TKI, donor lymphocyte infusion: DLI, and TKI + DLI) for relapsed disease post-alloBMT. Forty-five (63%) patients relapsed post-alloBMT (molecular relapse: n = 16, cytogenetic relapse: n = 20, hematologic relapse: n = 2, advanced phase relapse: n = 7) and 40 patients underwent one of three treatments: TKI-only (n = 13), DLI-only (n = 11) or TKI + DLI (n = 16). Although not statistically significant, the TKI-only group had the highest cumulative incidence of CMR and lowest cumulative incidence of death compared to DLI and TKI + DLI. These data support the finding that TKI therapy is active in the post-alloBMT setting.
异基因骨髓移植(alloBMT)后复发的慢性髓性白血病(CML)的最佳治疗方法尚不清楚。我们对1995年至2008年期间连续71例接受alloBMT治疗CML的患者进行了单中心回顾性分析。使用多状态模型来量化alloBMT后完全分子反应(CMR)和死亡的累积发生率。主要分析是比较alloBMT后复发疾病的三种治疗干预措施(酪氨酸激酶抑制剂:TKI、供体淋巴细胞输注:DLI和TKI + DLI)。45例(63%)患者alloBMT后复发(分子复发:n = 16,细胞遗传学复发:n = 20,血液学复发:n = 2,晚期复发:n = 7),40例患者接受了三种治疗之一:仅TKI(n = 13)、仅DLI(n = 11)或TKI + DLI(n = 16)。与DLI和TKI + DLI相比,仅TKI组的CMR累积发生率最高,死亡累积发生率最低,尽管无统计学意义。这些数据支持TKI治疗在alloBMT后环境中有效的发现。