Department of Oncology and Radiotherapy, Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru; Centro de Medicina de Precisión, Universidad de San Martin de Porres, Lima, Peru.
Department of Oncology and Radiotherapy, Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru.
Clin Lymphoma Myeloma Leuk. 2019 Sep;19(9):e551-e557. doi: 10.1016/j.clml.2019.06.005. Epub 2019 Jun 15.
The red blood cell distribution width (RDW) is an easy-to-obtain laboratory value that has emerged as a potential prognostic factor in solid and hematologic malignancies.
We evaluated 121 patients with de novo diffuse large B-cell lymphoma (DLBCL) treated with standard chemoimmunotherapy at our institution between 2010 and 2012. We categorized patients with high RDW (> 14.6%) and normal RDW (11.6%-14.6%). We fitted multivariate regression models for complete response (CR) and overall survival (OS).
Patients with high RDW were less likely to achieve CR to chemoimmunotherapy than patients with normal RDW (48% vs. 83%; P < .001). The 5-year OS rate for patients with high RDW was lower than in patients with normal RDW (51% vs. 79%; P = .001). In multivariate regression models, high RDW was independently associated with lower odds of achieving CR (odds ratio, 0.32; 95% confidence interval [CI], 0.12-0.83; P = .02) and with higher risk of death from any cause (hazard ratio [HR], 2.04; 95% CI, 1.03-4.02; P = .04) than normal RDW in patients with DLBCL treated with chemoimmunotherapy. High RDW remained an independent adverse factor for OS after adjustment for the International Prognostic Index and the National Comprehensive Cancer Network-International Prognostic Index scores with HR 2.20 (95% CI, 1.12-4.31; P = .02) and HR 2.67 (95% CI 1.28-5.59; P = .009), respectively.
High RDW appears to be an adverse predictive and prognostic factor in patients with de novo DLBCL treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone).
红细胞分布宽度(RDW)是一种易于获得的实验室值,已成为实体瘤和血液恶性肿瘤的潜在预后因素。
我们评估了 2010 年至 2012 年在我院接受标准化疗免疫治疗的 121 例新发弥漫性大 B 细胞淋巴瘤(DLBCL)患者。我们将 RDW 高(> 14.6%)和 RDW 正常(11.6%-14.6%)的患者进行分类。我们为完全缓解(CR)和总生存(OS)拟合了多变量回归模型。
与 RDW 正常的患者相比,RDW 高的患者对化疗免疫治疗更不可能达到 CR(48% vs. 83%;P <.001)。RDW 高的患者 5 年 OS 率低于 RDW 正常的患者(51% vs. 79%;P =.001)。在多变量回归模型中,RDW 与较低的 CR 几率(比值比,0.32;95%置信区间 [CI],0.12-0.83;P =.02)和更高的任何原因死亡风险(风险比 [HR],2.04;95% CI,1.03-4.02;P =.04)独立相关。在调整国际预后指数和国家综合癌症网络-国际预后指数评分后,RDW 仍然是 DLBCL 患者化疗免疫治疗后 OS 的独立不良因素,HR 为 2.20(95% CI,1.12-4.31;P =.02)和 HR 为 2.67(95% CI,1.28-5.59;P =.009)。
RDW 似乎是接受 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松)治疗的新发 DLBCL 患者的不良预测和预后因素。