首页> 美国卫生研究院文献>Frontiers in Oncology >Feasibility of Induction Docetaxel Cisplatin 5-Fluorouracil Cetuximab (TPF-C) Followed by Concurrent Cetuximab Radiotherapy for Locally Advanced Head and Neck Squamous Cell Carcinoma
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Feasibility of Induction Docetaxel Cisplatin 5-Fluorouracil Cetuximab (TPF-C) Followed by Concurrent Cetuximab Radiotherapy for Locally Advanced Head and Neck Squamous Cell Carcinoma

机译:诱导多西他赛顺铂5-氟尿嘧啶西妥昔单抗(TPF-C)继之以西妥昔单抗同期放疗治疗局部晚期头颈部鳞状细胞癌的可行性

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摘要

>Purpose: To report our experience with a sequential regimen of induction TPF-C followed by radioimmunotherapy with cetuximab in patients with locally advanced head and neck squamous cell carcinoma (HNSCC).>Patients and Methods: Toxicity and outcome was retrospectively analyzed in 22 patients receiving sequential therapy with induction TPF-C followed by radioimmunotherapy between October 2008 and December 2011. Outcome was estimated using Kaplan–Meier analyses. In addition, we performed mutation analysis for PIK3CA genes and high risk HPV DNA detection using PCR.>Results: Mean time of follow-up was 16 months. Six patients were TNM Stage III, 15 patients IV (IVA or IVB), and one patient Stage II with bulky disease. During TPF-C, Grade 3 and 4 toxicities occurred in eight patients, dose modifications in seven, delays in one, and unplanned admissions in five. Clinical tumor response was documented in 18 of the 21 patients who completed at least three cycles of TPF-C with three patients developing complete response and 15 partial responses. Grade 3/4 mucositis was observed in six patients. At a median follow-up of 19 months, 13 patients were alive and nine had died including seven patients as a result of disease persistence or recurrence and two as a result of unrelated causes. PIK3CA mutations were not identified and our two oropharynx cases were HPV negative.>Conclusion: The combination of induction TPF-C with concurrent cetuximab radioimmunotherapy in patients with locally advanced HNSCC is tolerable, with encouraging efficacy.
机译:>目的:要报告我们在局部晚期头颈部鳞状细胞癌(HNSCC)患者中采用TPF-C诱导顺序疗法和西妥昔单抗放射免疫疗法的经验。>患者和方法:< / strong>回顾性分析了2008年10月至2011年12月接受序贯诱导TPF-C放射免疫治疗的22例患者的毒性和预后。结果采用Kaplan-Meier分析评估。此外,我们对PIK3CA基因进行了突变分析,并使用PCR检测了高危HPV DNA。>结果:平均随访时间为16个月。 6例患者为TNM III期,15例IV(IVA或IVB),1例II期大体积疾病。在TPF-C期间,八名患者发生了3级和4级毒性,七名患者发生了剂量调整,一例出现延误,五例发生了计划外入院。在至少完成三个TPF-C周期的21例患者中,有18例记录了临床肿瘤反应,其中3例出现了完全缓解和15例部分缓解。六例患者观察到3/4级粘膜炎。在19个月的中位随访中,有13例患者存活,9例死亡,其中7例由于疾病持续或复发而死亡,2例因不相关原因而死亡。未发现PIK3CA突变,我们的两个口咽部病例均为HPV阴性。

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