Study to evaluate the acute toxicities and response to concurrent chemoradiotherapy with weekly cisplatin versus cisplatin and paclitaxel in locally advanced head-and-neck cancer

T. Jacob, Sandesh Rao, D. Fernandes, Lanisha Sequeira, HKrishna Raj
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Abstract

Objective: The objective of this study is to assess the acute toxicities and locoregional response rates in patients with locally advanced head-and-neck squamous cell carcinomas with intensity-modulated radiotherapy (IMRT) and weekly cisplatin versus weekly cisplatin and paclitaxel. Methodology: Fifty-four patients with histologically proven squamous cell carcinoma of the head and neck at the department of radiotherapy, at our hospital, were taken up for this study. Patients were allotted to the study and control arm and results were analyzed. All patients were treated with IMRT 70 Gy along with weekly injection cisplatin 35 mg/m2 (control arm) versus IMRT 70 Gy along with weekly injection paclitaxel 30 mg/m2 and injection cisplatin 20 mg/m2 (study arm). The toxicity profile was assessed weekly during treatment and then monthly for 3 months postchemoradiotherapy with Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. The immediate locoregional response rates were assessed clinically postchemoradiotherapy and then monthly for 3 months after concurrent chemoradiotherapy. Results: In this study, oropharyngeal cancer dominated with 52% of patients in the study arm and 47% in the control arm. Most of the patients were in Stage IV a (69%). Toxicities were observed more in the study arm with 59% of patients with Grade 3 mucositis and 52% of patients with Grade 3 dermatitis. Eighty-one percent of patients in the study arm and 70% of patients in the control arm had Grade 3 dysphagia. Grade 2 leukocytopenia was seen in 44% of patients in the study arm and 19% in the control arm. Complete and partial responses at the end of follow-up were 70% and 30% in the study arm and 48% and 52% in the control arm, respectively. Conclusion: Concurrent chemoradiotherapy with injection cisplatin and paclitaxel in locally advanced squamous cell carcinoma of the head and neck has a higher complete response rate with manageable toxicities.
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评估每周顺铂与顺铂和紫杉醇同步放化疗对局部晚期头颈癌的急性毒性和反应的研究
目的:本研究的目的是评估局部晚期头颈部鳞状细胞癌患者接受调强放疗(IMRT)和每周一次顺铂治疗与每周一次顺铂和紫杉醇治疗的急性毒性和局部区域反应率。方法:选取我院放疗科54例经组织学证实的头颈部鳞状细胞癌患者作为研究对象。将患者分为研究组和对照组,并对结果进行分析。所有患者均接受IMRT治疗70 Gy,每周注射顺铂35 mg/m2(对照组),而IMRT治疗70 Gy,每周注射紫杉醇30 mg/m2,注射顺铂20 mg/m2(研究组)。在治疗期间每周评估毒性概况,然后在放化疗后3个月内每月评估一次,使用不良事件通用术语标准(CTCAE) 5.0版本。在放化疗后临床评估即时局部反应率,然后在同步放化疗后每月评估3个月。结果:在本研究中,口咽癌占主导地位,研究组患者占52%,对照组患者占47%。大多数患者处于IV期a(69%)。在研究组中,59%的3级黏膜炎患者和52%的3级皮炎患者观察到更多的毒性。研究组81%的患者和对照组70%的患者患有3级吞咽困难。研究组44%的患者出现2级白细胞减少症,对照组19%。随访结束时,研究组的完全缓解率和部分缓解率分别为70%和30%,对照组为48%和52%。结论:顺铂联合紫杉醇同步放化疗治疗局部晚期头颈部鳞状细胞癌完全缓解率高,毒副反应可控。
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27
审稿时长
11 weeks
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