Outcome of relapse after allogeneic stem cell transplant in patients with acute myeloid leukemia

被引:46
作者
Devillier, Raynier [1 ]
Crocchiolo, Roberto [1 ]
Etienne, Anne [1 ]
Prebet, Thomas [1 ]
Charbonnier, Aude [1 ]
Fuerst, Sabine [1 ]
El-Cheikh, Jean [1 ]
D'Incan, Evelyne [1 ]
Rey, Jerome [1 ]
Faucher, Catherine [1 ]
Blaise, Didier [1 ,2 ]
Vey, Norbert [1 ,2 ]
机构
[1] Inst J Paoli I Calmettes, Dept Hematol, F-13009 Marseille, France
[2] Aix Marseille Univ, Marseille, France
关键词
Acute myeloid leukemia; allogeneic stem cell transplantation; relapse; BONE-MARROW TRANSPLANTATION; ACUTE MYELOGENOUS LEUKEMIA; INTERMEDIATE-DOSE CYTARABINE; GEMTUZUMAB OZOGAMICIN; THERAPY; AML; CHEMOTHERAPY; AZACITIDINE; RECOMMENDATIONS; DIAGNOSIS;
D O I
10.3109/10428194.2012.741230
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although allogeneic stem cell transplant (Allo-SCT) is an effective treatment for high-risk acute myeloid leukemia (AML), relapses remain a major cause of treatment failure. There is currently no standard of care for post-transplant relapse of AML, but the increasing numbers of investigational agents in this setting require a better knowledge of their outcome. We retrospectively evaluated the efficacy of salvage therapies in 54 patients with AML relapsing after Allo-SCT. Twenty-four patients received intensive salvage treatment (17 non-intensive chemotherapy, 13 supportive care). Complete remissions (CRs) were seen only in the group who received intensive salvage (CR rate: 17/24 [71%]). One-year overall survival was 19% (median: 3.4 months) in the whole study group and 33% in the intensive savage group (vs. 7% for patients without intensive salvage, p = 0.004). Factors influencing overall survival (OS) were: time to relapse after Allo-SCT (hazard ratio [HR]: 3.7 [1.6-8.8]) and performance status (PS) at relapse (HR: 2.2 [1.1-4.4]) by multivariate analysis. Our results confirm the poor prognosis of AML relapse after Allo-SCT. In selected patients salvage chemotherapy produces CRs, but these are short lived. Other strategies aiming at modulating immune antileukemic activity have to be developed.
引用
收藏
页码:1228 / 1234
页数:7
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