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个体合并症对异基因造血干细胞移植后非复发死亡率的影响。

The impact of individual comorbidities on non-relapse mortality following allogeneic hematopoietic stem cell transplantation.

机构信息

Hematology and Bone Marrow Transplantation Division, Chaim Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel.

Service d'Hématologie Clinique et de Thérapie Cellulaire, Hôpital Saint-Antoine, Paris, France.

出版信息

Leukemia. 2018 Aug;32(8):1787-1794. doi: 10.1038/s41375-018-0185-y. Epub 2018 Jun 27.

Abstract

Comorbidity burden is a well-established risk factor for non-relapse mortality (NRM) following allogeneic stem cell transplantation (allo-SCT). We evaluated whether individual comorbidities could better characterize NRM risk. Furthermore, given differing toxicity profiles of conditioning agents, we hypothesized that the hazard of comorbidities is exerted in a regimen-specific manner. This retrospective study included 875 adults treated with an allo-SCT. Six conditioning regimens were considered. Across the entire cohort and within each regimen, the hazard ratio (HR) for NRM associated with individual comorbidities was assessed using multivariable Cox regressions. In the overall population, renal dysfunction, hypoalbuminemia, and severe hepatic disease were associated with the highest risk of NRM (HR 2.1, HR 1.9, HR 1.7, respectively). The risk associated with specific comorbidities was modified by the conditioning regimen and was not correlated with intensity. In patients conditioned with fludarabine/busulfan (Flu/Bu4), NRM risk was increased with cardiac disease (HR 5.54). Severe pulmonary disease and a pre-existing infection were associated with increased NRM risk in patients receiving fludarabine/melphalan (HR 4.9) and fludarabine/treosulfan (HR 3.6), respectively. Comorbidities may exert effects unique to particular conditioning regimens, suggesting that regimen selection should be driven in part by specific comorbidities.

摘要

合并症负担是异基因干细胞移植(allo-SCT)后非复发死亡率(NRM)的一个既定危险因素。我们评估了个体合并症是否可以更好地描述 NRM 风险。此外,鉴于预处理方案的毒性特征不同,我们假设合并症的危害以方案特异性的方式发挥作用。这项回顾性研究纳入了 875 名接受 allo-SCT 治疗的成年人。考虑了六种预处理方案。在整个队列和每个方案中,使用多变量 Cox 回归评估与个体合并症相关的 NRM 的风险比(HR)。在整个人群中,肾功能不全、低白蛋白血症和严重肝疾病与 NRM 的风险最高(HR 分别为 2.1、1.9 和 1.7)。特定合并症的风险受预处理方案的影响,并与强度无关。在接受氟达拉滨/白消安(Flu/Bu4)预处理的患者中,心脏病(HR 5.54)与 NRM 风险增加相关。在接受氟达拉滨/美法仑(HR 4.9)和氟达拉滨/替莫唑胺(HR 3.6)预处理的患者中,严重肺部疾病和先前存在的感染与 NRM 风险增加相关。合并症可能对特定预处理方案产生独特的影响,这表明方案选择部分应受特定合并症的驱动。

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