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首页> 外文期刊>Journal of Clinical Oncology >CD6+ donor marrow T-cell depletion as the sole form of graft-versus-host disease prophylaxis in patients undergoing allogeneic bone marrow transplant from unrelated donors.
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CD6+ donor marrow T-cell depletion as the sole form of graft-versus-host disease prophylaxis in patients undergoing allogeneic bone marrow transplant from unrelated donors.

机译:CD6 +供体骨髓T细胞耗竭是预防从无关供体接受同种异体骨髓移植的患者的移植物抗宿主疾病的唯一形式。

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PURPOSE: The role of donor marrow T-cell depletion (TCD) in preventing graft-versus-host disease (GVHD) after transplantation of unrelated allogeneic marrow remains undefined. Because different TCD methodologies differ in the degree and specificity with which T cells are removed, it is likely that transplant outcomes would depend on which technique is used. Herein, we report results in the first 48 recipients of unrelated marrow using CD6+ TCD as the sole form of GVHD prophylaxis. PATIENTS AND METHODS: Median age of patients was 46 years (20 to 58 years). Donors were matched at A/B HLA loci. Ablation consisted of cyclophosphamide and fractionated total-body irradiation (TBI; 14 Gy). To facilitate engraftment, patients also received 7.5 Gy (22 points) or 4.5 Gy (26 points) of total lymphoid irradiation (TLI) before admission. No additional immune suppressive prophylaxis was administered. Granulocyte colony-stimulating factor was administered daily from day +1 to engraftment. RESULTS: All 48 patients demonstrated neutrophil engraftment. An absolute neutrophil count of 500 x 10(6)/L was achieved at a median of 12 days (range, 9 to 23 days). There were no cases of late graft failure. The number of CD34+ cells infused/kg was associated with speed of platelet and neutrophil recovery. The dose of TLI did not influence engraftment. Grades 2-4 acute GVHD occurred in 42% of patients (95% confidence interval [CI], 0.28 to 0.57). Mortality at day 100 was 19%. There have been only five relapses. Estimated 2-year survival was 44% (95% CI, 0.28 to 0.59) for the entire group, 58% for patients less than 50 years of age. In multivariable analysis, age less than 50 years (P =.002), cytomegalovirus seronegative status (P =.04), and early disease status at bone marrow transplant (P =.05) were associated with superior survival. CONCLUSION: CD6+ TCD does not impede engraftment of unrelated bone marrow after low-dose TLI, cyclophosphamide, and TBI. CD6+ TCD as the sole form of GVHD prophylaxis results in an incidence of GVHD that compares favorably with many adult studies of unrelated transplantation using unmanipulated marrow and immune-suppressive medications, especially in light of the median age of our patients (46 years). Although event-free survival in patients less than 50 years of age is very encouraging, older patients experience frequent transplantation-related complications despite TCD.
机译:目的:供体骨髓T细胞耗竭(TCD)在预防无关的异体骨髓移植后预防移植物抗宿主病(GVHD)中的作用尚不清楚。由于不同的TCD方法在去除T细胞的程度和特异性上不同,因此移植结果可能取决于所使用的技术。在本文中,我们报告了使用CD6 + TCD作为预防GVHD的唯一形式的无关骨髓的前48位接受者的结果。患者与方法:患者的中位年龄为46岁(20至58岁)。在A / B HLA基因座处配对供体。消融包括环磷酰胺和全身照射(TBI; 14 Gy)。为了促进植入,患者在入院前还接受了7.5 Gy(22分)或4.5 Gy(26分)的总淋巴照射(TLI)。没有额外的免疫抑制预防措施。从第+1天到植入,每天给予粒细胞集落刺激因子。结果:全部48例患者均出现中性粒细胞植入。中位数为12天(范围为9到23天),中性粒细胞绝对计数为500 x 10(6)/ L。没有晚期移植失败的情况。输注的CD34 +细胞数量/ kg与血小板和中性粒细胞恢复的速度有关。 TLI的剂量不影响植入。 42%的患者发生2-4级急性GVHD(95%置信区间[CI],0.28至0.57)。第100天的死亡率为19%。只有五次复发。整个组的2年生存率估计为44%(95%CI,0.28至0.59),小于50岁的患者为58%。在多变量分析中,年龄小于50岁(P = .002),巨细胞病毒血清阴性状态(P = .04)和骨髓移植早期疾病状态(P = .05)与较高的生存率相关。结论:低剂量TLI,环磷酰胺和TBI后,CD6 + TCD不会阻止无关骨髓的植入。作为预防GVHD的唯一形式,CD6 + TCD导致GVHD的发生率,与许多成人使用未经处理的骨髓和免疫抑制药物进行的不相关移植的研究相比,尤其是根据我们患者的中位年龄(46岁)来进行研究。尽管50岁以下患者的无事件存活率非常令人鼓舞,但尽管有TCD,老年患者仍会发生与移植相关的并发症。

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