Middeke Jan Moritz, Herbst Regina, Parmentier Stefani, Bug Gesine, Hänel Mathias, Stuhler Gernot, Schäfer-Eckart Kerstin, Rösler Wolf, Klein Stefan, Bethge Wolfgang, Bitz Ulrich, Büttner Bozena, Knoth Holger, Alakel Nael, Schaich Markus, Morgner Anke, Kramer Michael, Sockel Katja, von Bonin Malte, Stölzel Friedrich, Platzbecker Uwe, Röllig Christoph, Thiede Christian, Ehninger Gerhard, Bornhäuser Martin, Schetelig Johannes
Universitätsklinikum Carl Gustav Carus der TU Dresden, Medizinische Klinik und Poliklinik I, Dresden, Germany.
Medizinische Klinik III, Klinikum Chemnitz, Chemnitz, Germany.
Biol Blood Marrow Transplant. 2017 Sep;23(9):1491-1497. doi: 10.1016/j.bbmt.2017.05.014. Epub 2017 May 17.
In patients with relapsed or refractory (r/r) acute myeloid leukemia (AML), allogeneic hematopoietic stem cell transplantation (HSCT) is considered to be the only treatment providing long-term disease control. The BRIDGE trial studied the safety and efficacy of a clofarabine-based salvage therapy before HSCT in patients with r/r AML. Here, we report the long-term follow-up of this phase II multicenter trial and exploratory analyses on the impact of comorbidity on outcome. Eighty-four patients with a median age of 61 years (range, 40 to 75) were enrolled. Patients were scheduled for at least 1 cycle of salvage therapy with CLARA (clofarabine 30 mg/m; cytarabine 1 g/m, days 1 to 5). Chemo-responsive patients with a donor received HSCT after first CLARA. The conditioning regimen consisted of clofarabine 30 mg/m, day -6 to -3, and melphalan 140 mg/m day -2. The Eastern Cooperative Oncology Group (ECOG) score, the hematopoietic cell transplantation-specific comorbidity index (HCT-CI), and the Cumulative Illness Rating Scale were obtained at study enrollment as well as before HSCT. Sixty-seven percent of the patients received HSCT within the trial. After a median follow up of 40 months, the estimated 3-year overall survival (OS) for all enrolled patients and those with HSCT within the trial was 40% and 55%, respectively. Relapse-free survival for patients who underwent transplantation with a complete remission afterwards (n = 50) was 48%, calculated from the day of transplantation. In multivariate analysis, both the HCT-CI and ECOG score had a statistically significant impact on OS with a hazard ratio of 1.22 (P = .025)and 1.72 (P = .001), respectively. Using a clofarabine-based salvage therapy combined with early allogeneic HSCT, we were able to achieve good long-term results for patients with r/r AML. In this cohort, both the HCT-CI and the ECOG scores gave prognostic information on OS, showing the feasibility and clinical relevance of comorbidity evaluation at the time of diagnosis of r/r AML patients.
在复发或难治性(r/r)急性髓系白血病(AML)患者中,异基因造血干细胞移植(HSCT)被认为是唯一能提供长期疾病控制的治疗方法。BRIDGE试验研究了以氯法拉滨为基础的挽救疗法在r/r AML患者HSCT前的安全性和疗效。在此,我们报告这项II期多中心试验的长期随访情况以及关于合并症对预后影响的探索性分析。84例患者入组,中位年龄61岁(范围40至75岁)。患者计划接受至少1周期的CLARA挽救治疗(氯法拉滨30mg/m²;阿糖胞苷1g/m²,第1至5天)。化疗反应良好且有供者的患者在首次CLARA治疗后接受HSCT。预处理方案包括氯法拉滨30mg/m²,第-6至-3天,美法仑140mg/m²第-2天。在研究入组时以及HSCT前获取东部肿瘤协作组(ECOG)评分、造血细胞移植特异性合并症指数(HCT-CI)和累积疾病评定量表。67%的患者在试验期间接受了HSCT。中位随访40个月后,所有入组患者以及试验期间接受HSCT患者的估计3年总生存期(OS)分别为40%和55%。移植后达到完全缓解的患者(n = 50)的无复发生存期从移植日起计算为48%。在多变量分析中,HCT-CI和ECOG评分对OS均有统计学显著影响,风险比分别为1.22(P = 0.025)和1.72(P = 0.001)。使用以氯法拉滨为基础的挽救疗法联合早期异基因HSCT,我们能够为r/r AML患者取得良好的长期结果。在这个队列中,HCT-CI和ECOG评分均给出了关于OS的预后信息,显示了在r/r AML患者诊断时进行合并症评估的可行性和临床相关性。