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使用 HLA 配型相合同胞以外的供者进行白血病异基因骨髓移植的结果。

Results of allogeneic bone marrow transplants for leukemia using donors other than HLA-identical siblings.

作者信息

Szydlo R, Goldman J M, Klein J P, Gale R P, Ash R C, Bach F H, Bradley B A, Casper J T, Flomenberg N, Gajewski J L, Gluckman E, Henslee-Downey P J, Hows J M, Jacobsen N, Kolb H J, Lowenberg B, Masaoka T, Rowlings P A, Sondel P M, van Bekkum D W, van Rood J J, Vowels M R, Zhang M J, Horowitz M M

机构信息

International Bone Marrow Transplant Registry, Health Policy Institute, Medical College of Wisconsin, Milwaukee, USA.

出版信息

J Clin Oncol. 1997 May;15(5):1767-77. doi: 10.1200/JCO.1997.15.5.1767.

Abstract

PURPOSE

To compare outcomes of bone marrow transplants for leukemia from HLA-identical siblings, haploidentical HLA-mismatched relatives, and HLA-matched and mismatched unrelated donors.

PATIENTS

A total of 2,055 recipients of allogeneic bone marrow transplants for chronic myelogenous leukemia (CML), acute myelogenous leukemia (AML), and acute lymphoblastic leukemia (ALL) were entered onto the study. Transplants were performed between 1985 and 1991 and reported to the International Bone Marrow Transplant Registry (IBMTR). Donors were HLA-identical siblings (n = 1,224); haploidentical relatives mismatched for one (n = 238) or two (n = 102) HLA-A, -B, or -DR antigens; or unrelated persons who were HLA-matched (n = 383) or mismatched for one HLA-A, -B, or -DR antigen (n = 108). HLA typing was performed using serologic techniques.

RESULTS

Transplant-related mortality was significantly higher after alternative donor transplants than after HLA-identical sibling transplants. Among patients with early leukemia (CML in chronic phase or acute leukemia in first remission), 3-year transplant-related mortality (+/-SE) was 21% +/- 2% after HLA-identical sibling transplants and greater than 50% after all types of alternative donor transplants studied. Among patients with early leukemia, relative risks of treatment failure (inverse of leukemia-free survival), using HLA-identical sibling transplants as the reference group, were 2.43 (P < .0001) with 1-HLA-antigen-mismatched related donors, 3.79 (P < .0001) with 2-HLA-antigen-mismatched related donors, 2.11 (P < .0001) with HLA-matched unrelated donors, and 3.33 (P < .0001) with 1-HLA-antigen-mismatched unrelated donors. For patients with more advanced leukemia, differences in treatment failure were less striking: 1-HLA-antigen-mismatched relatives, 1.22 (P = not significant [NS]); 2-HLA-antigen-mismatched relatives, 1.81 (P < .0001); HLA-matched unrelated donors, 1.39 (P = .002); and 1-HLA-antigen-mismatched unrelated donors, 1.63 (P = .002).

CONCLUSION

Although transplants from alternative donors are effective in some patients with leukemia, treatment failure is higher than after HLA-identical sibling transplants. Outcome depends on leukemia state, donor-recipient relationship, and degree of HLA matching. In early leukemia, alternative donor transplants have a more than twofold increased risk of treatment failure compared with HLA-identical sibling transplants. This difference is less in advanced leukemia.

摘要

目的

比较来自 HLA 全相合同胞、单倍型 HLA 不相合亲属以及 HLA 相合和不相合非血缘供者的白血病骨髓移植结果。

患者

共有 2055 例接受异基因骨髓移植治疗慢性粒细胞白血病(CML)、急性髓细胞白血病(AML)和急性淋巴细胞白血病(ALL)的受者纳入本研究。移植于 1985 年至 1991 年间进行,并报告给国际骨髓移植登记处(IBMTR)。供者为 HLA 全相合同胞(n = 1224);单倍型 HLA 不相合亲属,其中一个(n = 238)或两个(n = 102)HLA - A、-B 或 -DR 抗原不相合;或 HLA 相合(n = 383)或一个 HLA - A、-B 或 -DR 抗原不相合(n = 108)的非血缘供者。采用血清学技术进行 HLA 分型。

结果

替代供者移植后的移植相关死亡率显著高于 HLA 全相合同胞移植。在早期白血病患者(慢性期 CML 或首次缓解期急性白血病)中,HLA 全相合同胞移植后 3 年移植相关死亡率(±SE)为 21%±2%,而在所研究的所有类型替代供者移植后均超过 50%。在早期白血病患者中,以 HLA 全相合同胞移植作为参照组,治疗失败(无白血病生存的倒数)的相对风险在 1 个 HLA 抗原不相合的相关供者中为 2.43(P <.0001),在 2 个 HLA 抗原不相合的相关供者中为 3.79(P <.0001),在 HLA 相合的非血缘供者中为 2.11(P <.0001),在 1 个 HLA 抗原不相合的非血缘供者中为 3.33(P <.0001)。对于病情较晚期的白血病患者,治疗失败的差异不那么显著:1 个 HLA 抗原不相合的亲属,1.22(P = 无显著性差异[NS]);2 个 HLA 抗原不相合的亲属,1.81(P <.0001);HLA 相合的非血缘供者,1.39(P =.002);1 个 HLA 抗原不相合的非血缘供者,1.63(P =.002)。

结论

尽管来自替代供者的移植对一些白血病患者有效,但治疗失败率高于 HLA 全相合同胞移植。结果取决于白血病状态、供受者关系以及 HLA 匹配程度。在早期白血病中,替代供者移植的治疗失败风险比 HLA 全相合同胞移植增加两倍多。在晚期白血病中这种差异较小。

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