Bolwell B, Pohlman B, Kalaycio M, Wise K, Goormastic M, Andresen S
Department of Hematology and Medical Oncology, and Transplant Center, Cleveland Clinic Foundation, OH, USA.
Bone Marrow Transplant. 1999 Jul;24(1):53-5. doi: 10.1038/sj.bmt.1701812.
We have anecdotally noted that serum LDH values rise after the infusion of autologous peripheral blood progenitor cells (PBPCs), presumably the result of cellular lysis. To further study this issue, we retrospectively reviewed 203 consecutive patients undergoing autologous PBPC transplant from August 1996 to December 1997. 194 patients were evaluable, having documented LDH values on day -1 to day +5 post-transplant. All patients received cytokine mobilization for PBPC collection, and 99% received a chemotherapy-only preparative regimen. 99% of patients had a rise in serum LDH after PBPC infusion. 76% had a normal LDH prior to PBPC infusion that became abnormally high after infusion; 22% began with an abnormally high value that became higher with the infusion of PBPCs. The LDH rose at least 50% in 91% of patients. 92% of the patients had their peak LDH value occur on day +1 post-transplant. The total dose of CD34+ cells infused negatively correlated with peak percentage change of LDH (P = 0.0007). This result was initially perplexing, as we believed that a higher number of infused cells would correlate with a higher LDH value as a result of in vivo cellular lysis. However, the total number of CD34+ cells also negatively correlated with the number of phereses required to collect our threshold of 2.0 x 10(6) CD34+ cells/kg (P = 0.0001). After adjusting for CD34+ cell dose, we found that the number of phereses correlated highly with a peak percentage of change of LDH (P = 0.001). We conclude that the serum LDH increases universally after autologous PBPC infusion, peaking on day +1. We believe that this rise in serum LDH is a result of cell lysis that occurs ex vivo, and correlates with the number of pheresis procedures required to collect an adequate number of CD34+ cells. This may be a result of increasing red blood cell contamination with more phereses, and resultant RBC hemolysis.
我们经观察发现,输注自体外周血祖细胞(PBPCs)后血清乳酸脱氢酶(LDH)值会升高,推测这是细胞裂解的结果。为进一步研究此问题,我们回顾性分析了1996年8月至1997年12月期间连续接受自体外周血祖细胞移植的203例患者。194例患者可进行评估,记录了移植后第 -1天至第 +5天的LDH值。所有患者均接受细胞因子动员以采集外周血祖细胞,99%的患者接受了仅含化疗的预处理方案。99%的患者在输注外周血祖细胞后血清LDH升高。76%的患者在输注外周血祖细胞前LDH正常,输注后变得异常升高;22%的患者开始时LDH值异常高,输注外周血祖细胞后更高。91%的患者LDH至少升高50%。92%的患者LDH峰值出现在移植后第 +1天。输注的CD34+细胞总剂量与LDH峰值变化百分比呈负相关(P = 0.0007)。这一结果最初令人困惑,因为我们认为输注细胞数量越多,由于体内细胞裂解,LDH值会越高。然而,CD34+细胞总数也与采集达到我们设定的每千克2.0×10(6)个CD34+细胞阈值所需的单采次数呈负相关(P = 0.0001)。在调整CD34+细胞剂量后,我们发现单采次数与LDH峰值变化百分比高度相关(P = 0.001)。我们得出结论,自体外周血祖细胞输注后血清LDH普遍升高,在第 +1天达到峰值。我们认为血清LDH的升高是体外发生的细胞裂解的结果,并且与采集足够数量的CD34+细胞所需的单采程序次数相关。这可能是由于更多次单采导致红细胞污染增加以及由此产生的红细胞溶血所致。