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作为新诊断多发性骨髓瘤患者生存预测指标的平台期时间。

Time to plateau as a predictor of survival in newly diagnosed multiple myeloma.

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Division of Hematology, Mayo Clinic, Rochester, Minnesota.

出版信息

Am J Hematol. 2018 Jul;93(7):889-894. doi: 10.1002/ajh.25113.

Abstract

Response rates in newly diagnosed multiple myeloma have improved dramatically with the introduction of highly effective novel therapies. However, survival in patients achieving optimal responses to initial treatment can vary significantly, and new prognostic indicators are required to improve risk stratification. We investigated the relationship between time to plateau (T ) and survival in 1099 newly diagnosed patients treated with novel agents at our institution from 2005 to 2015. T was defined as time from initiation of first-line therapy to best response to first-line therapy. The median T was 4.9 months (0.7-58.6) and plateau duration was 1.8 years (0.2-11.0). Patients who required > 120 days to achieve a plateau had longer modified overall survival (mOS) and progression free survival (mPFS) calculated from a landmark of best response (P < .001 for both comparisons). Statistically significant improvement in mOS was retained in subgroup analysis based on age and whether patients received upfront autologous hematopoietic stem cell transplantation (ASCT) (P < .001 for all comparisons). Our results suggest that patients who respond more gradually to initial therapy (T  > 120 days) experience longer survival compared to more rapid responders. Patients with a prolonged T could represent an "ongoing responder" phenotype that portends a survival advantage independent of treatment with upfront ASCT, depth of response, and biologic markers such as ISS stage and cytogenetic risk.

摘要

新诊断多发性骨髓瘤患者的缓解率随着高效新型疗法的引入而显著提高。然而,初始治疗达到最佳反应的患者的生存情况可能有很大差异,需要新的预后指标来改善风险分层。我们研究了本机构 2005 年至 2015 年接受新型药物治疗的 1099 例新诊断患者的平台期时间(T)与生存之间的关系。T 定义为从一线治疗开始到一线治疗最佳反应的时间。中位 T 为 4.9 个月(0.7-58.6),平台期持续时间为 1.8 年(0.2-11.0)。达到平台期需要>120 天的患者,从最佳反应的里程碑开始计算,其改良总生存期(mOS)和无进展生存期(mPFS)更长(两者比较均 P<.001)。基于年龄和患者是否接受 upfront 自体造血干细胞移植(ASCT)的亚组分析中,mOS 统计学上显著改善(所有比较均 P<.001)。我们的结果表明,与快速应答者相比,初始治疗(T>120 天)应答更缓慢的患者的生存时间更长。T 延长的患者可能代表一种“持续应答”表型,与 upfront ASCT、应答深度以及 ISS 分期和细胞遗传学风险等生物学标志物独立预示着生存优势。

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