Gao Hongye, Liu Yanfei, Xu Yanfeng, Mi Lan, Zhang Chen, Wang Xiaopei, Song Yuqin, Zhu Jun, Liu Weiping
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, No. 52 Fucheng Road, Haidian District, Beijing 100142, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, No. 52 Fucheng Road, Haidian District, Beijing 100142, China.
J Formos Med Assoc. 2022 Dec;121(12):2556-2565. doi: 10.1016/j.jfma.2022.06.003. Epub 2022 Jul 1.
The actual relative dose intensity (RDI) of the attenuated R-CCOP regimen (rituximab, cytoxan, pegylated liposomal doxorubicin [PLD], vincristine, and prednisone) has not been fully investigated in Chinese geriatric patients with diffuse large B-cell lymphoma (DLBCL). In particular, the optimum dose for PLD remains unclear.
We retrospectively collected clinical data from patients with untreated DLBCL aged 65-80 years subsequently treated with the R-CCOP. The restricted cubic spline model (RCS) was used to test the non-linear relationship between the predictors and outcomes.
Eighty-four patients were enrolled, with a median age of 73.5 years. More than half of the patients (54.8%) received at least 6 cycles. The median dose per cycle of cytoxan and PLD were 605.5 and 19.9 mg/m. The 5-year progression-free survival (PFS), overall survival rate, and disease-specific survival rates were 38.7%, 44.8%, and 57.2%, respectively. The RDI of PLD (PLD-RDI, <70% vs ≥ 70%) was only significant in the univariate analysis (P = 0.002) but not in the multivariate analysis. The RCS model showed a decreasing trend of hazards with an increasing PLD dose per cycle after adjustment. No significant difference was observed between the low- and high-risk groups with PLD-RDI ≥ 70% (P = 0.548). However, patients in the high-risk group had unfavorable PFS with PLD-RDI < 70% (P = 0.006).
The optimal dose of PLD for elderly patients with DLBCL in China remains to be determined. Evaluating the tolerance and identifying risk categories are critical for clinical decision-making in this population.
在中国老年弥漫性大B细胞淋巴瘤(DLBCL)患者中,尚未充分研究减量化R-CCOP方案(利妥昔单抗、环磷酰胺、聚乙二醇化脂质体阿霉素[PLD]、长春新碱和泼尼松)的实际相对剂量强度(RDI)。特别是,PLD的最佳剂量仍不清楚。
我们回顾性收集了65-80岁未经治疗的DLBCL患者随后接受R-CCOP治疗的临床数据。采用受限立方样条模型(RCS)检验预测因素与结局之间的非线性关系。
共纳入84例患者,中位年龄73.5岁。超过一半的患者(54.8%)接受了至少6个周期的治疗。环磷酰胺和PLD的中位每周期剂量分别为605.5和19.9mg/m。5年无进展生存期(PFS)、总生存率和疾病特异性生存率分别为38.7%、44.8%和57.2%。PLD的RDI(PLD-RDI,<70% vs≥70%)仅在单因素分析中有显著性(P = 0.002),而在多因素分析中无显著性。RCS模型显示,调整后每周期PLD剂量增加,风险呈下降趋势。PLD-RDI≥70%的低风险组和高风险组之间未观察到显著差异(P = 0.548)。然而,PLD-RDI<70%的高风险组患者的PFS较差(P = 0.006)。
中国老年DLBCL患者的PLD最佳剂量仍有待确定。评估耐受性和识别风险类别对于该人群的临床决策至关重要。