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Paraproteinaemia after allo-SCT, association with alemtuzumab-based conditioning and CMV reactivation.

机译:异基因SCT后的副蛋白血症,与基于阿仑单抗的调节和CMV激活相关。

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Paraproteinaemia following allo-SCT is common. We analysed 91 consecutive patients undergoing allo-SCT; conditioning included alemtuzumab in 42% of the patients. Paraproteinaemia incidence at 2 years was 32%. In univariate analysis paraproteinaemia was associated with unrelated donor, age, recipient seropositivity for CMV and alemtuzumab conditioning (hazard ratio (HR) 3.93, P=0.0006). Paraproteinaemia was not associated with haematological diagnosis; disease status at transplant; varicella zoster, herpes simplex or EBV serology; reduced-intensity vs myeloablative conditioning or GVHD. CMV reactivation-more frequent in alemtuzumab recipients-was associated with paraproteinaemia (HR 7.52, P<0.0001). In multivariate analysis, only increasing age (HR 1.04 per year, P=0.048) and CMV reactivation (HR 5.74, P=0.001) were significantly associated with paraproteinaemia. Alemtuzumab without CMV reactivation, however, resulted in significantly more paraproteinaemia, suggesting an effect that is independent of CMV reactivation. OS was poorer in patients with paraproteinaemia (HR 2.54, P=0.04) and relapse increased (HR 2.38, P=0.087). Paraproteinaemia was not significantly independently associated with decreased survival on multivariate analysis. Post transplant paraproteinaemia is associated with CMV reactivation, is more frequent in alemtuzumab-conditioned transplants and is not associated with improved OS.
机译:异源SCT后的副蛋白血症很常见。我们分析了连续91例接受allo-SCT的患者。在42%的患者中,调理包括alemtuzumab。 2年时副蛋白血症的发生率为32%。在单变量分析中,副蛋白血症与无关的供体,年龄,接受者的CMV血清阳性和Alemtuzumab调节相关(危险比(HR)3.93,P = 0.0006)。副蛋白血症与血液学诊断无关。移植时的疾病状况;水痘带状疱疹,单纯疱疹或EBV血清学;强度降低与清髓调理或GVHD相比。 CMV激活-在Alemtuzumab受体中更频繁-与副蛋白血症相关(HR 7.52,P <0.0001)。在多变量分析中,仅年龄增长(每年HR 1.04,P = 0.048)和CMV激活(HR 5.74,P = 0.001)与副蛋白血症显着相关。但是,没有CMV激活的Alemtuzumab导致明显更高的副蛋白血症,提示这种作用独立于CMV激活。副蛋白血症患者的OS较差(HR 2.54,P = 0.04),复发率增加(HR 2.38,P = 0.087)。在多因素分析中,副蛋白血症与存活率降低并没有显着独立相关。移植后蛋白血症与CMV激活有关,在以阿仑单抗为条件的移植物中更常见,并且与OS改善无关。

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