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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >The Effect of Bone Marrow Plasma Cell Burden on Survival in Patients with Light Chain Amyloidosis Undergoing High-Dose Melphalan and Autologous Stem Cell Transplantation
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The Effect of Bone Marrow Plasma Cell Burden on Survival in Patients with Light Chain Amyloidosis Undergoing High-Dose Melphalan and Autologous Stem Cell Transplantation

机译:大剂量美法兰和自体干细胞移植对轻链淀粉样变性病患者骨髓浆细胞负荷的影响

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摘要

The prognosis in light chain (AL) amyloidosis has been linked to several variables, which are primarily related to end-organ damage. Recently, bone marrow plasma cell (BMPC) burden >10% has also been described as an adverse prognostic factor. We reviewed data pertaining to 546 patients with AL amyloidosis who underwent high-dose melphalan (HDM) and stem cell transplantation (SCT) to determine if BMPC> 10% was a negative prognostic factor. Of these patients, 445 had a BMPC burden 5 10% and 101 had a BMPC burden > 10%. Patients with BMPC > 30% were excluded from the study. The median overall survival (OS) was 7.86 years (95% confidence interval [CI], 6.69 to 9.83) in patients with BMPC <= 10% and 6.8 years (95% CI, 5.75 to 10.17) for those with BMPC >10% (hazard ratio, 1.106; 95% CI, .78 to 1.45; P = .70) after HDM/SCT. Of the 101 patients with a BMPC burden > 10%, 25 received induction therapy. The median OS was 7.78 years (95% CI, 5.4 to 13.4) for those without induction therapy and 5.75 years (95% CI, 3.94 to not available; P=.28) for those with induction therapy. Furthermore, hematologic response and relapse rates did not differ in these 2 groups after HDM/SCT. We conclude that BMPC > 10% and < 30% is not a poor prognostic factor with respect to survival in patients with AL amyloidosis treated with HDM/SCT and that induction therapy in this group does not impact OS. (C) 2016 American Society for Blood and Marrow Transplantation.
机译:轻链(AL)淀粉样变性的预后与几个变量有关,这些变量主要与终末器官损害有关。最近,> 10%的骨髓浆细胞(BMPC)负担也被描述为不良预后因素。我们回顾了546例接受大剂量美法仑(HDM)和干细胞移植(SCT)的AL淀粉样变性患者的数据,以确定BMPC> 10%是否为阴性预后因素。在这些患者中,445的BMPC负担为5 10%,而101的BMPC负担> 10%。 BMPC> 30%的患者被排除在研究之外。 BMPC <= 10%的患者的中位总体生存期(OS)为7.86年(95%置信区间[CI],从6.69至9.83),而BMPC> 10%的患者的中位总体生存期(OS)为6.8年(95%CI,5.75至10.17) (危险比1.106; 95%CI:0.78至1.45; P = 0.70)。在BMPC负担> 10%的101例患者中,有25例接受了诱导治疗。没有诱导治疗的患者的中位OS为7。78年(95%CI,5.4-13.4),有诱导治疗的患者的中位OS为5。75年(95%CI,3.94(无资料); P = .28)。此外,HDM / SCT后两组的血液学反应和复发率无差异。我们得出的结论是,对于接受HDM / SCT治疗的AL淀粉样变性患者,BMPC> 10%和<30%并非生存不良的预后因素,并且该组的诱导治疗不会影响OS。 (C)2016美国血液和骨髓移植学会。

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