Grim Jiří, Hroch Miloš, Chládek Jaroslav, Petera Jiří, Martínková Jiřina
Department of Oncology and Radiotherapy, University Hospital, Sokolská Street, 500 05, Hradec Králové, Czech Republic,
Clin Pharmacokinet. 2015 May;54(5):503-15. doi: 10.1007/s40262-014-0216-4.
This study estimated patients' early response following neoadjuvant chemoradiotherapy (CHRT) of locally advanced rectal cancer based on 5-fluorouracil (5-FU). The target was to achieve pathological complete response (pCR; residual disease-free stage) and toxicities of grade ≤2, using individual dosing predicted according to the steady-state plasma concentration (C ss) and pharmacokinetic parameters of 5-FU: the area under the time-concentration curve at steady state (AUC) and clearance (CL).
This open-label prospective study enrolled 33 adult patients treated with 5-FU administered as a continuous intravenous infusion over 4-5 weeks, as follows: in Group 1a (N = 6), the patients received a standard dose of 300 mg/m(2)/24 h. In Group 1b (N = 7), the patients were treated with an escalated dose of 400-1,000 mg/m(2)/24 h. In Group 2 (N = 20), the patients were given dosing kinetically guided in order to reach the target range of 5-FU C ss 50-100 µg/L. Tolerability was tested according to Common Terminology Criteria for Adverse Events v3.0 (CTCAE). Radiotherapy was delivered with 10-15 MV photon beams at 1.8 Gy/fraction up to 50.4 Gy in 28 daily fractions for 5 days a week. Surgery followed 4-6 weeks after the completion of CHRT and clinical restaging. The pCR and residual tumour stage were evaluated using preoperative tumour downstaging in magnetic resonance, postoperative histopathological staging and tumour regression rate (residual disease).
The cumulative AUC of 5-FU (total exposure to the drug) correlated with cumulative 5-FU dose (r = 0.61; p < 0.001) and residual disease (r s = -0.53; p < 0.005). A higher target pCR rate was reached in patients individually treated (Group 2) who finished the whole 5-week CHRT. The individual daily dose needed to reach the target C ss should be >350 mg/m(2) (up to 600 mg/m(2)) provided that 5-FU metabolic ratio is within the range of 2.5-6 and the cumulative AUC5wks is within 50-100 mg·h/L.
本研究基于5-氟尿嘧啶(5-FU)评估局部晚期直肠癌患者新辅助放化疗(CHRT)后的早期反应。目标是实现病理完全缓解(pCR;无残留病灶阶段)且毒性≤2级,采用根据5-FU的稳态血浆浓度(C ss)及药代动力学参数预测的个体化给药:稳态时的时间-浓度曲线下面积(AUC)和清除率(CL)。
这项开放标签的前瞻性研究纳入了33例成年患者,接受5-FU持续静脉输注治疗4 - 5周,具体如下:在1a组(N = 6),患者接受300 mg/m²/24 h的标准剂量。在1b组(N = 7),患者接受400 - 1000 mg/m²/24 h的递增剂量治疗。在2组(N = 20),患者接受动力学指导给药,以达到5-FU C ss 50 - 100 μg/L的目标范围。根据不良事件通用术语标准v3.0(CTCAE)测试耐受性。放疗采用10 - 15 MV光子束,每次1.8 Gy,每周5天,共28次,总剂量达50.4 Gy。在CHRT完成及临床重新分期后4 - 6周进行手术。使用术前磁共振肿瘤降期、术后组织病理学分期及肿瘤退缩率(残留病灶)评估pCR和残留肿瘤分期。
5-FU的累积AUC(药物总暴露量)与5-FU累积剂量相关(r = 0.61;p < 0.001),与残留病灶相关(r s = -0.53;p < 0.005)。完成整个5周CHRT的个体化治疗患者(2组)达到了更高的目标pCR率。若5-FU代谢率在2.5 - 6范围内且5周累积AUC在50 - 100 mg·h/L内,达到目标C ss所需的个体化每日剂量应>350 mg/m²(最高600 mg/m²)。