T-cell depletion of HLA-identical transplants in leukemia.

T-cell depletion of HLA-identical transplants in leukemia.
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DOI:
10.1182/blood.v78.8.2120.2120
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发表时间:
1991-10
期刊:
影响因子:
20.3
通讯作者:
A. M. Marmont;M. Horowitz;R. Gale;K. Sobocinski;Robert;-C.;Ash;Dirk W. van Bekkum;Richard;-E.;Champlin;K. A. Dicke;J. Goldman;Robert A. Good;R. Herzig;Richard Hong;Tohru Masaoka;A. Rimm;Olle Ringdh;Bruno Wilhelm Speck;Roy;Weiner;M. Bortin
A. M. Marmont;M. Horowitz;R. Gale;K. Sobocinski;Robert;-C.;Ash;Dirk W. van Bekkum;Richard;-E.;Champlin;K. A. Dicke;J. Goldman;Robert A. Good;R. Herzig;Richard Hong;Tohru Masaoka;A. Rimm;Olle Ringdh;Bruno Wilhelm Speck;Roy;Weiner;M. Bortin
中科院分区:
医学1区
文献类型:
--
作者:
A. M. Marmont;M. Horowitz;R. Gale;K. Sobocinski;Robert;-C.;Ash;Dirk W. van Bekkum;Richard;-E.;Champlin;K. A. Dicke;J. Goldman;Robert A. Good;R. Herzig;Richard Hong;Tohru Masaoka;A. Rimm;Olle Ringdh;Bruno Wilhelm Speck;Roy;Weiner;M. Bortin

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我们通过比较731例T细胞耗竭移植和2,480例非T细胞耗竭移植,分析了T细胞耗竭对HLA相合同胞骨髓移植治疗白血病的结果的影响。T细胞耗竭降低急性移植物抗宿主病(GVHD)(相对危险度[RR] 0.45; P <0.0001)和慢性(GVHD)(RR 0.56; P <0.0001)。然而,它增加了移植失败(RR 9.29; P小于0.0001)。白血病复发率也增加。在首次缓解的急性白血病或慢性期慢性粒细胞白血病中,去除T细胞的移植后白血病复发的可能性是其他患者的2.75倍(P <0.0001)。T细胞耗竭增加了治疗失败的风险(RR 1.35; P <0.0003),并降低了无白血病生存率。我们还研究了与T细胞耗竭移植结果相关的可控变量。独特的发现是,在接受T细胞耗竭移植治疗早期白血病的受者中,辐射剂量大于或等于11戈伊,(RR 0.54; P小于.01),剂量率大于14 cGy/min(RR 0.56; P <0.002),以及单独使用环孢霉素的额外移植后免疫抑制(RR 0.53; P小于0.0006)或环孢霉素联合甲氨蝶呤(RR 0.36; P小于0.01)与较少的治疗失败相关。使用单克隆抗体而不是物理技术进行T细胞去除(RR 2.01; P小于0.03)和分次放疗(RR 1.69; P小于0.05)与治疗失败率增加和无白血病生存率降低相关。这些数据可能有助于设计策略,以改善T细胞耗竭移植的结果。
We analyzed the effects of T-cell depletion on the outcome of HLA-identical sibling bone marrow transplants for leukemia by comparing 731 T-cell-depleted transplants with 2,480 non-T-cell-depleted transplants. T-cell depletion decreased acute graft-versus-host disease (GVHD) (relative risk [RR] 0.45; P less than .0001) and chronic (GVHD) (RR 0.56; P less than .0001). However, it increased graft failure (RR 9.29; P less than .0001). Leukemia relapse also was increased. In first remission acute leukemia or chronic phase chronic myelogenous leukemia, leukemia relapse was 2.75 times more likely after T-cell-depleted transplants (P less than .0001). T-cell depletion increased the risk of treatment failure (RR 1.35; P less than .0003) and decreased leukemia-free survival. We also studied controllable variables associated with outcome of T-cell-depleted transplants. The unique findings were that among recipients of T-cell-depleted transplants for early leukemia, radiation doses greater than or equal to 11 Gy (RR 0.54; P less than .01), dose rates greater than 14 cGy/min (RR 0.56; P less than .002), and additional posttransplant immune suppression with cyclosporine alone (RR 0.53; P less than .0006) or cyclosporine plus methotrexate (RR 0.36; P less than .01) were associated with fewer treatment failures. Use of monoclonal antibodies rather than physical techniques for T-cell depletion (RR 2.01; P less than .03) and fractionated radiation (RR 1.69; P less than .05) were associated with increased treatment failure and lower leukemia-free survival. These data may be useful in designing strategies to improve results of T-cell-depleted transplants.