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在首次分子缓解的成人低危和中危急性髓细胞白血病患者中,无关供者与自体移植的比较。

Unrelated matched versus autologous transplantation in adult patients with good and intermediate risk acute myelogenous leukemia in first molecular remission.

机构信息

Department of Hematology and Cell Therapy and EBMT Paris Office, Hôpital Saint-Antoine APHP, INSERM U 938, Université Pierre et Marie Curie UPMC, Paris, France.

Department of Oncology, University Hospital Bern, 3010, Bern, Switzerland.

出版信息

Am J Hematol. 2017 Dec;92(12):1318-1323. doi: 10.1002/ajh.24904. Epub 2017 Sep 28.

Abstract

Patients with Acute Myelogenous Leukemia have a better outcome if reaching molecular remission. We compared the outcome of 373 patients autografted and 335 patients allografted with a 10/10 compatible unrelated donor in first molecular remission. Patients were stratified using the ELN European Leukemia Net classification. ELN favorable group: (234 auto and 70 unrelated transplants). By univariate analysis, in the auto group, the Non Relapse Mortality (NRM) was lower (3.7% versus 19%; P < 10 ), Relapse Incidence (RI) higher (29% versus 17%, P < 10 ), Leukemia Free Survival (LFS) identical (67% versus 64%) and Overall Survival (OS) better than in the allogeneic group (83% versus 62%; P = .008). By multivariate analysis, autologous transplantation was associated with a lower NRM (HR: 4, P = .01) and a better OS (HR: 2.08, P = .04). ELN intermediate group 1: (87 autologous and 172 unrelated transplants). By univariate analysis, in the auto group, NRM was lower (2.5% versus 11.8%; P = .03), RI higher (59% versus 18%, P < 10 ), LFS lower (39% versus 70%; P < 10 ) and OS lower than in the unrelated donor group (61% versus 74%; P = .005). By multivariate analysis, unrelated donor was superior to autologous transplantation for LFS (HR: 0.36, P < 10 and OS (HR: 0.53, P = .01). ELN intermediate group 2: (52 autologous and 93 unrelated donors). The outcome was identical. We conclude that good risk patients get higher benefit from autologous transplantation. Intermediate risk 2 patients have the same outcome and Intermediate risk 1 patients get higher benefit from unrelated donor transplants.

摘要

如果急性髓系白血病患者达到分子缓解,其预后会更好。我们比较了 373 例接受自体移植和 335 例接受 10/10 相容非亲缘供体异基因移植的处于首次分子缓解期患者的结果。患者使用欧洲白血病网(ELN)分类进行分层。ELN 预后良好组:(234 例自体和 70 例非亲缘移植)。单因素分析显示,在自体组中,非复发死亡率(NRM)较低(3.7%对 19%;P<0.01),复发率(RI)较高(29%对 17%;P<0.01),无白血病生存率(LFS)相同(67%对 64%),总生存率(OS)优于异基因组(83%对 62%;P=0.008)。多因素分析显示,自体移植与较低的 NRM 相关(HR:4,P=0.01)和更好的 OS(HR:2.08,P=0.04)。ELN 中危 1 组:(87 例自体和 172 例非亲缘移植)。单因素分析显示,在自体组中,NRM 较低(2.5%对 11.8%;P=0.03),RI 较高(59%对 18%;P<0.01),LFS 较低(39%对 70%;P<0.01),OS 低于非亲缘供体组(61%对 74%;P=0.005)。多因素分析显示,非亲缘供体在 LFS(HR:0.36,P<0.01)和 OS(HR:0.53,P=0.01)方面优于自体移植。ELN 中危 2 组:(52 例自体和 93 例非亲缘供体)。结果相同。我们得出结论,低危患者从自体移植中获益更高。中危 2 组患者的结果相同,而中危 1 组患者从非亲缘供体移植中获益更高。

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