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急性白血病同基因造血干细胞移植的结果:首次完全缓解期接受移植的成人患者预后的危险因素

Results of syngeneic hematopoietic stem cell transplantation for acute leukemia: risk factors for outcomes of adults transplanted in first complete remission.

作者信息

Fouillard Loic, Labopin Myriam, Gratwohl Alois, Gluckman Eliane, Frassoni Francesco, Beelen Dietrich W, Willemze Roelof, Montserrat Emili, Blaise Didier, Atienza Arturo Iriondo, Sierra Jorge, Santos Moema, Gorin Norbert-Claude, Rocha Vanderson

机构信息

Department of Hematology, Hopital Saint-Antoine, AP-HP, 184 Rue du Faubourg Saint- Antoine, 75012 Paris, France.

出版信息

Haematologica. 2008 Jun;93(6):834-41. doi: 10.3324/haematol.11277. Epub 2008 May 10.

Abstract

BACKGROUND

The possibility of performing syngeneic hematopoietic stem cell transplantation is rare and there are concerns about the absence of a graft-versus-leukemia effect following such a strategy. We report the outcomes of a large series of adult patients who underwent syngeneic hematopoietic stem cell transplantation for acute myeloblastic leukemia or acute lymphoblastic leukemia.

DESIGN AND METHODS

The outcomes of all syngeneic transplants for acute myeloblastic or lymphoblastic leukemia reported to the European Group for Blood and Marrow Transplantation registry were analyzed; a study of prognostic factors was performed for those transplanted in first complete remission.

RESULTS

One hundred and sixty-two patients, 109 with acute myeloblastic leukemia and 53 with acute lymphoblastic leukemia, were identified; 116 were in first complete remission. Most of the patients did not receive prophylaxis against graft-versus-host disease. Nineteen patients developed acute graft-versus-host disease and only three patients developed chronic graft-versus-host disease. The median follow-up was 60 months. At 5 years the non-relapse mortality was 8 +/- 5%, the relapse incidence 49 +/- 8% and the leukemia-free survival 43 +/- 3%. The corresponding figures for patients in first complete remission were 7 +/- 2%, 40 +/- 4% and 53 +/- 5% at 5 years. Analysis of patients in first complete remission showed that the number of courses of chemotherapy required to induce first complete remission was the main risk factor: the leukemia-free survival at 5 years was 66 +/- 6% when first complete remission was reached after one induction course of chemotherapy and was only 20 +/- 9% when first complete remission was reached after at least two induction courses of chemotherapy (p = 0.0001); the relapse incidence was 30 +/- 6% and 54 +/- 10%, respectively (p = 0.007).

CONCLUSIONS

Outcomes were better for patients transplanted in first complete remission than in second complete remission or a more advanced phase of the disease. When a syngeneic donor is available for patients with high risk acute leukemia, allotransplantation should be performed as soon as the first complete remission has been achieved, ideally with one course of chemotherapy.

摘要

背景

进行同基因造血干细胞移植的可能性很小,且有人担心采用这种策略后会缺乏移植物抗白血病效应。我们报告了一大系列成年患者接受同基因造血干细胞移植治疗急性髓细胞白血病或急性淋巴细胞白血病的结果。

设计与方法

分析了向欧洲血液与骨髓移植组登记处报告的所有急性髓细胞或淋巴细胞白血病同基因移植的结果;对首次完全缓解期接受移植的患者进行了预后因素研究。

结果

共确定了162例患者,其中109例为急性髓细胞白血病,53例为急性淋巴细胞白血病;116例处于首次完全缓解期。大多数患者未接受移植物抗宿主病预防措施。19例患者发生了急性移植物抗宿主病,仅3例患者发生了慢性移植物抗宿主病。中位随访时间为60个月。5年时,非复发死亡率为8±5%,复发率为49±8%,无白血病生存率为43±3%。首次完全缓解期患者5年时的相应数据分别为7±2%、40±4%和53±5%。对首次完全缓解期患者的分析表明,诱导首次完全缓解所需的化疗疗程数是主要危险因素:化疗一个疗程后达到首次完全缓解时,5年无白血病生存率为66±6%,而至少两个疗程化疗后达到首次完全缓解时,5年无白血病生存率仅为20±9%(p = 0.0001);复发率分别为30±6%和54±10%(p = 0.007)。

结论

首次完全缓解期接受移植的患者比第二次完全缓解期或疾病更晚期的患者预后更好。当有同基因供体可用于高危急性白血病患者时,一旦达到首次完全缓解,应尽快进行异基因移植,理想情况是进行一个疗程的化疗。

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