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Recovery of polyclonal immunoglobulins one year after autologous stem cell transplantation as a long-term predictor marker of progression and survival in multiple myeloma

机译:自体干细胞移植一年后多克隆免疫球蛋白的恢复是多发性骨髓瘤进展和生存的长期预测指标

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Immunoparesis or suppression of polyclonal immunoglobulins is a very common condition in newly diagnosed myeloma patients. However, the recovery of polyclonal immunoglobulins in the setting of immune reconstitution after autologous stem cell transplantation and its effect on outcome has not yet been explored. We conducted this study in a cohort of 295 patients who had undergone autologous transplantation. In order to explore the potential role of immunoglubulin recovery as a dynamic predictor of progression or survival after transplantation, conditional probabilities of progression-free survival and overall survival were estimated according to immunoglobulin recovery at different time points using a landmark approach. One year after transplant, when B-cell reconstitution is expected to be completed, among 169 patients alive and progression free, 88 patients (52%) showed immunoglobulin recovery and 81 (48%) did not. Interestingly, the group with immunoglobulin recovery had a significantly longer median progression-free survival than the group with persistent immunoparesis (median 60.4 vs. 27.9 months, respectively; Hazard Ratio: 0.45, 95%Confidence Interval: 0.31–0.66; P <0.001), and improved overall survival (11.3 vs. 7.3 years; Hazard Ratio: 0.45, 95%Confidence Interval: 0.27–0.74; P =0.002). Furthermore, the percentage of normal plasma cells detected by flow cytometry in the bone marrow assessed at day 100 after transplantation was associated with the immunoglobulin recovery at that time and may predict immunoglobulin recovery in the subsequent months: nine months and one year. In conclusion, the recovery of polyclonal immunoglobulins one year after autologous transplantation in myeloma patients is an independent long-term predictor marker for progression and survival.
机译:在新诊断的骨髓瘤患者中,免疫抑制或多克隆免疫球蛋白的抑制是非常普遍的疾病。然而,尚未探索自体干细胞移植后免疫重建环境中多克隆免疫球蛋白的恢复及其对预后的影响。我们在295名接受自体移植的患者中进行了这项研究。为了探索免疫球蛋白恢复作为移植后进展或生存的动态预测指标的潜在作用,使用里程碑式方法根据免疫球蛋白在不同时间点的恢复情况,估算了无进展生存和总体生存的条件概率。移植后一年,预计B细胞重构将完成,在169例存活且无进展的患者中,有88例(52%)表现出免疫球蛋白恢复,而81例(48%)没有。有趣的是,具有免疫球蛋白恢复的组的中位无进展生存期比具有持续性免疫轻瘫的组要长得多(分别为中位数60.4和27.9个月;危险比:0.45,95%;置信区间:0.31-0.66; P <0.001) ,并提高了整体生存率(11.3年与7.3年;危险比:0.45,95%置信区间:0.27–0.74; P = 0.002)。此外,在移植后第100天通过流式细胞术检测到的骨髓中正常浆细胞的百分比与当时的免疫球蛋白恢复有关,并且可以预测随后的9个月和一年的免疫球蛋白恢复。总之,骨髓瘤患者自体移植一年后多克隆免疫球蛋白的恢复是进展和生存的独立长期预测指标。

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