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Treatment Outcome of Pharmacokinetics-Based Dosing of Docetaxel and Fluorouracil in Advanced Head and Neck Cancer Patients

机译:基于药代动力学的多西他赛和氟尿嘧啶在晚期头颈癌患者中的治疗结果

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Introduction: Docetaxel, Cisplatin and 5-Fluorouracil (DPF) became the standard induction chemotherapy in advanced Head and Neck Cancer (HNC) but associated with high toxicity rate. Several studies reported higher response rates with better tolerability when chemotherapy dose is calculated based on Pharmacokinetics (PK) versus conventional Body Surface Area (BSA). Patients and Methods: Thirty nine patients with stage III and IV HNC who received induction DPF were included in the study. Dose of cycle 1 was BSA-based then Docetaxel and 5-FU doses were PK-adjusted starting from cycle 2 whereas Cisplatin dose was BSA-based throughout the study. Results: After median follow up period of 14 months the overall survival (OS) and progression free survival (PFS) were 15.1 and 10.6 months respectively. Twenty nine patients were available for response assessment. Seven patients (23.3%) achieved complete response while partial response encountered in 20 patients (66.7%) with and Overall response rate of 89.6%. Both treatment related side effects and mortality significantly decreased after the application of PK dose adjustments (p-value 0.007 and 0.01 respectively). Conclusion: PK-guided dose adjustments of 5-FU and Docetaxel in DPF regimen can significantly decrease the treatment related side effects and mortality without compromising the tumor response rate. A randomized clinical trial is needed to compare the PK-guided dose adjustment with the standard BSA based protocol.
机译:简介:多西他赛,顺铂和5-氟尿嘧啶(DPF)成为晚期头颈癌(HNC)的标准诱导化疗,但毒性高。几项研究报告说,根据药代动力学(PK)相对常规体表面积(BSA)计算化疗剂量时,更高的反应率和更好的耐受性。 患者和方法:39例接受诱导DPF的III期和IV期HNC患者被纳入研究。周期1的剂量基于BSA,然后从周期2开始对多西他赛和5-FU剂量进行PK调整,而在整个研究中,顺铂剂量基于BSA。 结果:中位随访期为14个月后,总生存期(OS)和无进展生存期(PFS)分别为15.1和10.6个月。二十九名患者可用于反应评估。 7名患者(23.3%)达到完全缓解,而20例患者(66.7%)达到部分缓解,总缓解率为89.6%。应用PK剂量调整后,治疗相关的副作用和死亡率均显着降低(p值分别为0.007和0.01)。 结论:DPF方案中PK指导的5-FU和多西他赛剂量调整可以显着降低治疗相关的副作用和死亡率,而不会影响肿瘤的缓解率。需要一项随机临床试验来比较PK指导的剂量调整与基于标准BSA的方案。

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