Mehta J, Powles R, Singhal S, Horton C, Middleton G, Eisen T, Meller S, Pinkerton C R, Treleaven J
Leukaemia Unit. Royal Marsden Hospital, Surrey, UK.
Bone Marrow Transplant. 1997 Feb;19(4):349-55. doi: 10.1038/sj.bmt.1700657.
Allograft recipients are often unwell with significant organ dysfunction by the time delayed or failed engraftment is diagnosed. We attempted to identify factors associated with graft failure, or death due to infection, hemorrhage or graft failure in 712 patients undergoing allogeneic BMT. Low leukocyte counts between days 12 and 22 were strongly associated with subsequent graft failure or death. In multivariate analysis, a leukocyte count of < or = 0.2 x 10(9)/l on day 16 was the most powerful predictor of graft failure or death. Transplants from HLA-mismatched and unrelated donors were also associated with increased risk of both, and T cell depletion with increased risk of graft failure. On the basis of these findings, it may be possible to define graft failure in functional terms as early as 2 weeks after BMT rather than at 3 or 4 weeks. The use of growth factors can then be limited to patients most likely to benefit from them, and it may be possible to salvage patients at risk of complications of low counts early before their clinical condition deteriorates. We suggest that patients with leukocyte counts of 0.2 x 10(9)/l or less 14-16 days after BMT should be started on G-CSF or GM-CSF even if they are clinically well, and consideration should be given to a second infusion of cells.
在诊断出移植延迟或失败时,同种异体移植受者往往身体不适且伴有严重的器官功能障碍。我们试图在712例接受异基因骨髓移植的患者中确定与移植失败、或因感染、出血或移植失败导致死亡相关的因素。第12天至第22天白细胞计数低与随后的移植失败或死亡密切相关。多因素分析显示,第16天白细胞计数≤0.2×10⁹/L是移植失败或死亡的最强预测因素。来自HLA不匹配和无关供者的移植也与两者风险增加相关,而T细胞清除与移植失败风险增加相关。基于这些发现,有可能早在骨髓移植后2周而不是3或4周就从功能角度定义移植失败。然后,生长因子的使用可以仅限于最可能从中受益的患者,并且有可能在临床状况恶化之前尽早挽救有低细胞计数并发症风险的患者。我们建议,骨髓移植后14 - 16天白细胞计数为0.2×10⁹/L或更低的患者,即使临床状况良好,也应开始使用G - CSF或GM - CSF,并应考虑再次输注细胞。