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Efficacy of cisplatin-based immunochemotherapy plus alloSCT in high-risk chronic lymphocytic leukemia: final results of a prospective multicenter phase 2 HOVON study

机译:基于顺铂的免疫化学疗法和alloSCT在高危慢性淋巴细胞性白血病中的疗效:一项前瞻性多中心2期HOVON研究的最终结果

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Allogeneic stem cell transplantation (alloSCT) remains the only curative option for CLL patients. Whereas active disease at the time of alloSCT predicts poor outcome, no standard remission-induction regimen exists. We prospectively assessed outcome after cisplatin-containing immune-chemotherapy (R-DHAP) followed by alloSCT in 46 patients (median age 58 years) fulfilling modified European Society for Blood and Marrow Transplantation (EBMT) CLL Transplant Consensus criteria being refractory to or relapsed (R/R) <1 year after fludarabine or <2 years after fludarabine-based immunochemotherapy or R/R with del(17p). Twenty-nine patients received. >= 3 cycles of R-DHAP and sixteen <3 cycles (4 because of disease progression, 8 for toxicity and 4 toxic deaths). Overall rate of response to R-DHAP was 58%, 31 (67%) proceeded to alloSCT after conditioning with fludarabine and 2 Gy TBI. Twenty (65%) remained free from progression at 2 years after alloSCT, including 17 without minimal residual disease. Intention-to-treat 2-year PFS and overall survival of the 46 patients were 42 and 51% (35.5 months median follow-up); del(17p) or fludarabine refractoriness had no impact. R-DHAP followed by alloSCT is a reasonable treatment to be considered for high-risk CLL patients without access or resistance to targeted therapies.
机译:同种异体干细胞移植(alloSCT)仍然是CLL患者的唯一治疗选择。 alloSCT发生时的活动性疾病预后较差,但不存在标准的缓解诱导方案。我们对46例患者(中位年龄58岁)进行了含顺铂的免疫化学疗法(R-DHAP)继之以alloSCT评估,其结果符合修改后的欧洲血液和骨髓移植(EBMT)CLL移植耐受性或复发性标准(氟达拉滨后<1年或基于氟达拉滨的免疫化学疗法后<2年或del(17p)进行R / R。接受了29位患者。 > = 3个周期的R-DHAP和16个<3个周期(4个由于疾病进展,8个毒性和4个中毒死亡)。用氟达拉滨和2 Gy TBI调理后,对R-DHAP的总缓解率为58%,其中31(67%)接受了alloSCT。 alloSCT术后2年,仍有20例(65%)无进展,包括17例无最小残留病。意向治疗的2年PFS和46例患者的总生存率分别为42%和51%(中位随访35.5个月); del(17p)或氟达拉滨的耐火度没有影响。 R-DHAP联合alloSCT是对没有靶向疗法或没有靶向疗法耐药的高危CLL患者应考虑的合理治疗方法。

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