Rabitsch Werner, Böhm Alexandra, Bojic Marija, Schellongowski Peter, Wöhrer Stefan, Sliwa Thamer, Keil Felix, Worel Nina, Greinix Hildegard, Hauswirth Alexander, Kalhs Peter, Jaeger Ulrich, Valent Peter, Sperr Wolfgang R
Bone Marrow Transplantation Unit, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria; Intensive Care Unit, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
Eur J Clin Invest. 2014 Aug;44(8):775-83. doi: 10.1111/eci.12294.
Allogeneic haematopoietic stem cell transplantation (HSCT) is the only curative rescue therapy for patients (pts) with chemotherapy-refractory acute leukaemia. Disease control prior to HSCT is essential for long-term disease-free survival after HSCT.
We have retrospectively analysed the outcome of 20 pts aged 21-64 years with refractory leukaemia (acute myeloid leukaemia, n = 16; acute lymphatic leukaemia, n = 4) who received debulking therapy with clofarabine (10 mg/m², days 1-4) and cyclophosphamide (200 mg/m², days 1-4; ClofCy) prior to HSCT.
Clofarabine/cyclophosphamide (1-4 cycles) was well tolerated and resulted in a substantial reduction of leukaemic cells in all pts. HSCT was performed in 15 of 20 pts. After HSCT (myeloablative, n = 9; dose-reduced, n = 6), all pts showed engraftment and full donor chimerism (related donors, n = 4 or unrelated donors, n = 11) and all pts achieved complete haematologic remission (CR). The median survival after HSCT is 531 days (range: 48-1462 days), and six pts are still alive after a median of 1245 days. Seven pts died after they had relapsed between days +152 and +1496. One patient died from acute graft-versus-host disease (day +48) and one from systemic fungal infection (day +87).
Clofarabine/cyclophosphamide is a novel effective treatment approach for pts with chemotherapy-refractory acute leukaemia prior to HSCT. Whether this novel debulking protocol leads to improved long-term outcome in pts with refractory leukaemias remains to be determined in forthcoming clinical studies.
异基因造血干细胞移植(HSCT)是化疗难治性急性白血病患者唯一的根治性挽救治疗方法。HSCT前的疾病控制对于HSCT后的长期无病生存至关重要。
我们回顾性分析了20例年龄在21 - 64岁的难治性白血病患者(急性髓系白血病,n = 16;急性淋巴细胞白血病,n = 4)的治疗结果,这些患者在HSCT前接受了氯法拉滨(10 mg/m²,第1 - 4天)和环磷酰胺(200 mg/m²,第1 - 4天;ClofCy)的减瘤治疗。
氯法拉滨/环磷酰胺(1 - 4个周期)耐受性良好,所有患者的白血病细胞均显著减少。20例患者中有15例接受了HSCT。HSCT后(清髓性,n = 9;剂量降低,n = 6),所有患者均实现植入和完全供体嵌合(相关供体,n = 4或无关供体,n = 11),所有患者均实现完全血液学缓解(CR)。HSCT后的中位生存期为531天(范围:48 - 1462天),6例患者在中位1245天后仍存活。7例患者在+152天至+1496天之间复发后死亡。1例患者死于急性移植物抗宿主病(第48天),1例死于系统性真菌感染(第87天)。
氯法拉滨/环磷酰胺是HSCT前化疗难治性急性白血病患者的一种新型有效治疗方法。这种新型减瘤方案是否能改善难治性白血病患者的长期预后仍有待在即将开展的临床研究中确定。