Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Acta Pharmacol Sin. 2021 Apr;42(4):641-647. doi: 10.1038/s41401-020-0479-2. Epub 2020 Jul 31.
For follicular lymphoma (FL) with grade 1/2, the complete response (CR) rate of the first-line R-CHOP treatment was significantly low. In this study, we assessed the rationality of the administration of rituximab for FL patients with grade 1/2 based on concentration-response relationship analyses. Thus, we conducted a prospective pharmacokinetic (PK) study in 68 FL patients with grades 1-3 treated with R-CHOP at 21-day intervals. Plasma rituximab concentrations were quantified using ELISA and the population PK modeling was established with Phoenix NLME. The first cycle trough concentration (C) of rituximab was a significant independent risk factor for achieving CR in matched-pair logistic regression analysis, rather than the concentrations in later cycles; the recommendatory minimum optimal C was 13.60 μg/mL. Patients with grade 1/2 had significantly lower C compared with grade 3 (12.21 μg/mL vs. 23.45 μg/mL, P < 0.001), only 30% patients with grade 1/2 could reach 13.60 μg/mL, compared with 91.67% in patients with grade 3, which was in accord with its unsatisfactory CR rates (43.33% vs. 76.32%). The stage indicating the tumor burden (the target) was a crucial influence factor for C, accounting for 40.70% of its variability, 70% patients with grade 1/2 were stage IV in this study, since the systemic therapy only started at the disseminated disease stage. The initial dose of 1800 mg was recommended by Monte Carlo simulation for patients with grade 1/2. In summary, low C accounted for low-grade FL's unsatisfactory CR rate, designing the first dosage of rituximab should be a very important component of individualized therapy for FL.
对于 1/2 级滤泡性淋巴瘤 (FL),一线 R-CHOP 治疗的完全缓解 (CR) 率明显较低。在这项研究中,我们基于浓度-反应关系分析评估了给予 1/2 级 FL 患者利妥昔单抗的合理性。因此,我们对 68 例 1-3 级接受 21 天间隔 R-CHOP 治疗的 FL 患者进行了前瞻性药代动力学 (PK) 研究。采用 ELISA 定量检测利妥昔单抗的血浆浓度,并采用 Phoenix NLME 建立群体 PK 模型。在配对逻辑回归分析中,第一个周期的谷浓度 (C) 是 CR 的独立显著危险因素,而不是后续周期的浓度;推荐的最小最佳 C 为 13.60μg/ml。1/2 级患者的 C 明显低于 3 级(12.21μg/ml 比 23.45μg/ml,P<0.001),只有 30%的 1/2 级患者可达到 13.60μg/ml,而 3 级患者的比例为 91.67%,这与其 CR 率不理想(43.33%比 76.32%)相符。肿瘤负荷(靶器官)分期是 C 的关键影响因素,占其变异性的 40.70%,本研究中 70%的 1/2 级患者为 IV 期,因为只有在出现全身性疾病时才开始进行系统治疗。蒙特卡罗模拟推荐对 1/2 级患者给予 1800mg 的初始剂量。综上所述,低 C 导致低级别 FL 的 CR 率不理想,设计利妥昔单抗的初始剂量应该是 FL 个体化治疗的一个非常重要组成部分。