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高剂量化疗联合早期自体造血干细胞移植与标准剂量化疗或延迟移植治疗初诊多发性骨髓瘤的系统评价和荟萃分析。

High-Dose Chemotherapy with Early Autologous Stem Cell Transplantation Compared to Standard Dose Chemotherapy or Delayed Transplantation in Patients with Newly Diagnosed Multiple Myeloma: A Systematic Review and Meta-Analysis.

机构信息

Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona.

Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona.

出版信息

Biol Blood Marrow Transplant. 2019 Feb;25(2):239-247. doi: 10.1016/j.bbmt.2018.09.021. Epub 2018 Sep 20.

DOI:10.1016/j.bbmt.2018.09.021
PMID:30244101
Abstract

Autologous stem cell transplantation (SCT) is the standard of care for all transplantation-eligible patients diagnosed with multiple myeloma (MM). Various studies have compared clinical outcomes with frontline SCT ("early SCT") versus standard-dose therapy (SDT) alone, with or without salvage SCT ("SDT/late SCT"). In this meta-analysis, we compare overall survival (OS) and progression-free survival (PFS) outcomes between these 2 treatment approaches. Twelve studies were identified, including a total of 3633 patients, of whom 1811 received early SCT and 1822 received SDT/late SCT. In our analysis of all 12 studies, OS was not significantly different between the 2 groups (hazard ratio [HR], .86; 95% confidence interval [CI], .70 to 1.04), but PFS was better with early SCT (HR, .67; 95% CI, .54 to .82). In a subgroup analysis of 3 studies in which novel agents were used for induction, OS again was similar in the 2 groups, and PFS was favorable with early SCT (HR, .50; 95% CI, .36 to .70). This analysis shows that over the years, early SCT has been associated with prolonged PFS, but this did not consequently translate into prolonged OS in patients with newly diagnosed MM. The benefit of early SCT in terms of OS is less clear in the era of novel agents, given the limited follow-up of these studies.

摘要

自体干细胞移植(SCT)是所有符合移植条件的多发性骨髓瘤(MM)患者的标准治疗方法。多项研究比较了一线 SCT(“早期 SCT”)与单独标准剂量治疗(SDT),或与挽救性 SCT(“SDT/晚期 SCT”)联合治疗的临床结局。在这项荟萃分析中,我们比较了这两种治疗方法的总生存(OS)和无进展生存(PFS)结局。确定了 12 项研究,共纳入 3633 例患者,其中 1811 例接受早期 SCT,1822 例接受 SDT/晚期 SCT。在对所有 12 项研究的分析中,两组之间 OS 无显著差异(风险比[HR],0.86;95%置信区间[CI],0.70 至 1.04),但早期 SCT 的 PFS 更好(HR,0.67;95% CI,0.54 至 0.82)。在纳入新方案诱导的 3 项研究的亚组分析中,两组之间的 OS 再次相似,早期 SCT 的 PFS 更有利(HR,0.50;95% CI,0.36 至 0.70)。这项分析表明,多年来,早期 SCT 与延长的 PFS 相关,但这并没有导致新诊断 MM 患者的 OS 延长。鉴于这些研究的随访时间有限,在新型药物时代,早期 SCT 对 OS 的获益不太明确。

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