Division of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Division of Hematology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Tokyo, Japan.
Blood Adv. 2022 Jan 25;6(2):624-636. doi: 10.1182/bloodadvances.2021004607.
The standard treatment for adults with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) in Japan is imatinib-based chemotherapy followed by allogeneic hematopoietic stem cell transplantation (HSCT). However, ∼40% of patients cannot undergo HSCT in their first complete remission (CR1) because of chemotherapy-related toxicities or relapse before HSCT or older age. In this study, we evaluated dasatinib-based 2-step induction with the primary end point of 3-year event-free survival (EFS). The first induction (IND1) was dasatinib plus prednisolone to achieve CR, and IND2 was dasatinib plus intensive chemotherapy to achieve minimal residual disease (MRD) negativity. For patients who achieved CR and had an appropriate donor, HSCT during a consolidation phase later than the first consolidation, which included high-dose methotrexate, was recommended. Patients with pretransplantation MRD positivity were assigned to receive prophylactic dasatinib after HSCT. All 78 eligible patients achieved CR or incomplete CR after IND1, and 52.6% achieved MRD negativity after IND2. Nonrelapse mortality (NRM) was not reported. T315I mutation was detected in all 4 hematological relapses before HSCT. Fifty-eight patients (74.4%) underwent HSCT in CR1, and 44 (75.9%) had negative pretransplantation MRD. At a median follow-up of 4.0 years, 3-year EFS and overall survival were 66.2% (95% confidence interval [CI], 54.4-75.5) and 80.5% (95% CI, 69.7-87.7), respectively. The cumulative incidence of relapse and NRM at 3 years from enrollment were 26.1% and 7.8%, respectively. Dasatinib-based 2-step induction was demonstrated to improve 3-year EFS in Ph+ ALL. This study was registered in the UMIN Clinical Trial Registry as #UMIN000012173.
在日本,成人费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)的标准治疗是伊马替尼为基础的化疗,随后进行异基因造血干细胞移植(HSCT)。然而,由于化疗相关毒性或 HSCT 前复发或年龄较大,约 40%的患者无法在首次完全缓解(CR1)时进行 HSCT。在这项研究中,我们评估了基于达沙替尼的 2 步诱导,主要终点为 3 年无事件生存(EFS)。第 1 步诱导(IND1)为达沙替尼加泼尼松龙,以达到完全缓解(CR),第 2 步诱导(IND2)为达沙替尼加强化化疗,以达到微小残留病(MRD)阴性。对于达到 CR 且有合适供体的患者,建议在包括高剂量甲氨蝶呤的巩固期后进行移植后巩固期的 HSCT。在 HSCT 前 MRD 阳性的患者被分配接受预防性达沙替尼治疗。所有 78 名符合条件的患者在 IND1 后均达到 CR 或不完全 CR,52.6%的患者在 IND2 后达到 MRD 阴性。未报告非复发死亡率(NRM)。在 HSCT 前的所有 4 例血液学复发中均检测到 T315I 突变。58 名(74.4%)患者在 CR1 时进行了 HSCT,44 名(75.9%)患者在移植前 MRD 阴性。在中位随访 4.0 年后,3 年 EFS 和总生存率分别为 66.2%(95%CI,54.4-75.5)和 80.5%(95%CI,69.7-87.7)。从入组开始 3 年时,复发和 NRM 的累积发生率分别为 26.1%和 7.8%。基于达沙替尼的 2 步诱导被证明可提高 Ph+ALL 的 3 年 EFS。该研究在 UMIN 临床试验注册中心注册,编号为 #UMIN000012173。