Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, 9500 Euclid Ave, Cleveland, Ohio 44195.
Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio, 44195, USA.
Am J Hematol. 2017 Oct;92(10):989-996. doi: 10.1002/ajh.24819. Epub 2017 Jul 19.
International prognostic index (IPI) has remained the primary prognostic tool in diffuse large B cell lymphoma (DLBCL) for more than 20 years. Even though the disease is more common in older population, the impact of comorbidities, dose reductions, and treatment-related adverse events (TAEs) on the outcome in elderly DLBCL patients has not been well established. We studied 413 consecutive patients aged ≥ 60 years who were treated at the Cleveland Clinic. The median age at diagnosis was 69 years, 58% of patients had high IPI score, and 85% had low Charlson comorbidity index (CCI). Forty percent of patients required dose reductions during treatment, 78% achieved CR, and 70% experienced at least one grade II-IV TAE. High IPI score, high CCI, reduced dose chemotherapy, TAE, and hospitalization were significant predictors of death and relapse. In multivariable analysis, high IPI and CCI were independent predictors of overall and progression free survival. A simple model combining IPI and CCI could reliably distinguish three prognostically separate risk groups. Our results suggest that incorporation of CCI in current prognostic models can improve prognostication of older DLBCL patients and CCI might be a valuable tool in evaluating the eligibility of older patients for clinical trial enrollment.
国际预后指数(IPI)在弥漫性大 B 细胞淋巴瘤(DLBCL)中已经作为主要的预后工具超过 20 年。尽管该疾病在老年人群中更为常见,但合并症、剂量减少和与治疗相关的不良事件(TAE)对老年 DLBCL 患者结局的影响尚未得到充分证实。我们研究了在克利夫兰诊所治疗的 413 例连续的年龄≥60 岁的患者。诊断时的中位年龄为 69 岁,58%的患者具有高 IPI 评分,85%的患者具有低 Charlson 合并症指数(CCI)。40%的患者在治疗过程中需要减少剂量,78%的患者达到完全缓解,70%的患者经历至少 II-IV 级 TAE。高 IPI 评分、高 CCI、减少剂量化疗、TAE 和住院是死亡和复发的显著预测因素。多变量分析显示,高 IPI 和 CCI 是总生存和无进展生存的独立预测因素。一个简单的将 IPI 和 CCI 结合起来的模型可以可靠地区分三个预后不同的风险组。我们的研究结果表明,CCI 纳入目前的预后模型可以改善老年 DLBCL 患者的预后判断,CCI 可能是评估老年患者入组临床试验资格的有用工具。