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系统性轻链淀粉样变性患者接受风险调整美法仑和自体干细胞移植后的长期无事件生存率和总生存率。

Long-term event-free and overall survival after risk-adapted melphalan and SCT for systemic light chain amyloidosis.

作者信息

Landau H, Smith M, Landry C, Chou J F, Devlin S M, Hassoun H, Bello C, Giralt S, Comenzo R L

机构信息

Department of Medicine, New York-Presbyterian Hospital/Weill Cornell Medical College, New York, NY, USA.

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Leukemia. 2017 Jan;31(1):136-142. doi: 10.1038/leu.2016.229. Epub 2016 Aug 18.

Abstract

Stem cell transplantation (SCT), an effective therapy for amyloid light chain (AL) amyloidosis patients, is associated with low treatment-related mortality (TRM) with appropriate patient selection and risk-adapted dosing of melphalan (RA-SCT). Consolidation after SCT increases hematologic complete response (CR) rates and may improve overall survival (OS) for patients with <CR. We retrospectively analyzed outcomes for 143 patients who underwent RA-SCT with or without consolidation. Melphalan was administered at 100 (14%), 140 (52%) and 200 (34%) mg/m. The TRM rate at 100 days was 5%. RA-SCT resulted in CR in 24% (3 months) and 48% (12 months) of patients. The CR rate was particularly high (62%) in patients offered bortezomib consolidation. With a median follow-up among survivors of 7.7 years, median event-free survival (EFS) with RA-SCT was 4.04 years (95% confidence interval (CI): 3.41-5.01 years); median OS was 10.4 years (95% CI: 7.3-not achieved). Patients with CR at 12 months after SCT had significantly longer EFS (P=0.01) and OS (P=0.04). In a multivariate analysis, melphalan dose had no impact on EFS (P=0.26) or OS (P=0.11). For selected patients, RA-SCT was safe and was associated with extended long-term survival. With the availability of novel agents for consolidation, RA-SCT remains a very effective and important backbone treatment for AL amyloidosis.

摘要

干细胞移植(SCT)是治疗淀粉样轻链(AL)淀粉样变性患者的一种有效疗法,在进行适当的患者选择和马法兰风险适应性给药(RA-SCT)时,与较低的治疗相关死亡率(TRM)相关。SCT后的巩固治疗可提高血液学完全缓解(CR)率,并可能改善未达到CR的患者的总生存期(OS)。我们回顾性分析了143例行RA-SCT(无论是否进行巩固治疗)患者的结局。马法兰的给药剂量为100(14%)、140(52%)和200(34%)mg/m。100天时的TRM率为5%。RA-SCT使24%(3个月)和48%(12个月)的患者达到CR。接受硼替佐米巩固治疗的患者CR率特别高(62%)。在幸存者中,中位随访7.7年,RA-SCT的中位无事件生存期(EFS)为4.04年(95%置信区间(CI):3.41-5.01年);中位OS为10.4年(95%CI:7.3-未达到)。SCT后12个月达到CR的患者EFS(P=0.01)和OS(P=0.04)显著更长。在多变量分析中,马法兰剂量对EFS(P=0.26)或OS(P=0.11)无影响。对于选定的患者,RA-SCT是安全的,且与长期生存延长相关。随着新型巩固治疗药物的出现,RA-SCT仍然是AL淀粉样变性一种非常有效且重要的基础治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb02/5220129/714aaf63b2d6/leu2016229f1.jpg

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