Department of Pediatric Hematology-Oncology, Assistance Publique-Hôpitaux de Marseille, La Timone Hospital, Aix-Marseille University, Marseille, France; Department of Public Health, Laboratoire de Santé Publique (EA 3279) Research Unit, Marseille University Hospital, Aix-Marseille University, Marseille, France;
Department of Pediatric Hematology-Oncology, Assistance Publique-Hôpitaux de Marseille, La Timone Hospital, Aix-Marseille University, Marseille, France;
Blood. 2016 Jun 30;127(26):3450-7. doi: 10.1182/blood-2016-01-694349. Epub 2016 Apr 20.
Transplantation of 2 unrelated cord blood (UCB) units instead of 1 has been proposed to increase the cell dose. We report a prospective randomized study, designed to compare single- vs double-UCB transplantation in children and young adults with acute leukemia in remission or myelodysplasia. Eligible patients had at least two 4-6 HLA-identical UCBs with >3 × 10(7) nucleated cells/kg for the first and >1.5 × 10(7) for the second. The primary end point was the 2-year cumulative incidence of transplantation strategy failure, a composite end point including transplant-related mortality (TRM), engraftment failure, and autologous recovery. Randomized patients who did not proceed to transplantation due to refractory disease were considered transplantation failures. A total of 151 patients were randomized and included in the intent-to-treat analysis; 137 were transplanted. Double-UCB transplantation did not decrease transplantation strategy failure (23.4% ± 4.9% vs 14.9% ± 4.2%). Two-year posttransplant survival, disease-free survival, and TRM were 68.8% ± 6.0%, 67.6% ± 6.0%, and 5.9% ± 2.9% after single-unit transplantation compared with 74.8% ± 5.5%, 68.1% ± 6.0%, and 11.6% ± 3.9% after double-unit transplantation. The final relapse risk did not significantly differ, but relapses were delayed after double-unit transplantation. Overall incidences of graft-versus-host disease (GVHD) were similar, but chronic GVHD was more frequently extensive after double-UCB transplantation (31.9% ± 5.7% vs 14.7% ± 4.3%, P = .02). In an exploratory subgroup analysis, we found a significantly lower relapse risk after double-unit transplantation in patients receiving total body irradiation without antithymocyte globulin (ATG), whereas the relapse risk was similar in the group treated with busulfan, cyclophosphamide, and ATG. Single-UCB transplantation with adequate cell dose remains the standard of care and leads to low TRM. Double-unit transplantation should be reserved for patients who lack such units. This trial was registered at www.clinicaltrials.gov as #NCT01067300.
移植 2 份非相关脐带血(UCB)而不是 1 份已被提议增加细胞剂量。我们报告了一项前瞻性随机研究,旨在比较缓解期或骨髓增生异常的儿童和年轻成人中,单份与双份 UCB 移植的疗效。符合条件的患者至少有 2 份 4-6 个 HLA 完全匹配的 UCB,第 1 份 UCB 细胞数≥3×107/kg,第 2 份 UCB 细胞数≥1.5×107/kg。主要终点是移植策略失败的 2 年累积发生率,这是一个复合终点,包括移植相关死亡率(TRM)、植入失败和自体恢复。由于难治性疾病而未进行移植的随机患者被认为是移植失败。共纳入 151 例患者进行意向治疗分析;137 例患者接受了移植。双份 UCB 移植并未降低移植策略失败率(23.4%±4.9% vs. 14.9%±4.2%)。单份 UCB 移植后 2 年的移植后存活率、无病存活率和 TRM 分别为 68.8%±6.0%、67.6%±6.0%和 5.9%±2.9%,双份 UCB 移植后分别为 74.8%±5.5%、68.1%±6.0%和 11.6%±3.9%。最终复发风险无显著差异,但双份 UCB 移植后复发时间延迟。总体移植物抗宿主病(GVHD)发生率相似,但双份 UCB 移植后慢性 GVHD 更广泛(31.9%±5.7% vs. 14.7%±4.3%,P=0.02)。在探索性亚组分析中,我们发现未接受抗胸腺细胞球蛋白(ATG)的全身照射患者双份 UCB 移植后复发风险显著降低,而接受白消安、环磷酰胺和 ATG 治疗的患者复发风险相似。具有足够细胞剂量的单份 UCB 移植仍然是标准治疗方法,导致 TRM 低。双份 UCB 移植应保留给缺乏此类 UCB 的患者。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT01067300。