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低氧放射增敏剂尼莫唑在头颈部鳞状细胞癌(HNSCC)患者治疗中的依从性和毒性

Compliance and toxicity of the hypoxic radiosensitizer nimorazole in the treatment of patients with head and neck squamous cell carcinoma (HNSCC).

作者信息

Metwally Mohamed A Hassan, Frederiksen Katrine Diemer, Overgaard Jens

机构信息

Department of Experimental Clinical Oncology, Aarhus University Hospital , Aarhus , Denmark.

出版信息

Acta Oncol. 2014 May;53(5):654-61. doi: 10.3109/0284186X.2013.864050. Epub 2013 Dec 13.

Abstract

PURPOSE

To evaluate the compliance and toxicity of the hypoxic radiosensitizer nimorazole in head and neck cancer patients.

METHODS

A retrospective study of patients with head and neck squamous cell carcinoma (HNSCC), treated in Denmark between 1990 and 2013. All patients treated with radical radiotherapy (± chemotherapy) [66-70 Gy; 33-35 fractions; 2 Gy/fraction; 5-6 fractions/week] concomitant with the hypoxic radiosensitizer nimorazole. Nimorazole was administered as oral tablets in doses of approximately 1.2 g/m(2) body surface area in connection with the first of each daily radiation treatment. A second daily dose of 1 g was given in connection with the second radiotherapy fraction in the accelerated fractionation regimen. The compliance was estimated as the percentage of the initially prescribed dose, which was received by each patient. The main side effects were recorded.

RESULTS

A total of 1049 patients were investigated. The tolerance to nimorazole was fair: 58% of patients received the full prescribed total dose. Nausea and vomiting were the major complaints: among the 260 patients with dose reductions due to known side effects, (87%) were due to nausea/vomiting. All side effects ceased when treatment was interrupted, and neither severe nor long lasting side effects were observed. Female patients were significantly more likely to have dose reduction (OR 2.02; 95% CI 1.50-2.70), and nausea/vomiting. Patients aged more than 70 years were significantly more likely to have dose reduction. Patients who received less than 1100 mg/m(2) were significantly less likely to have dose reduction (OR 0.58; CI 0.44-0.78), and nausea/vomiting, compared to those who received 1100-1300 mg/m(2). The tolerance was also less in the group of patients received accelerated chemoradiotherapy (OR 1.70; CI 1.20-2.50) with more association with nausea/vomiting (OR 2.09; CI 1.40-3.10).

CONCLUSION

The compliance to nimorazole is fair, with tolerable acute, but neither persistent nor late, toxicity. It can be administered with chemotherapy and different radiotherapy fractionation schedules.

摘要

目的

评估乏氧放射增敏剂尼莫唑在头颈癌患者中的依从性和毒性。

方法

对1990年至2013年在丹麦接受治疗的头颈鳞状细胞癌(HNSCC)患者进行回顾性研究。所有患者均接受根治性放疗(±化疗)[66 - 70 Gy;33 - 35次分割;2 Gy/次分割;5 - 6次分割/周],同时使用乏氧放射增敏剂尼莫唑。尼莫唑以口服片剂形式给药,剂量约为1.2 g/m²体表面积,与每日第一次放射治疗同时进行。在加速分割方案中,与第二次放疗分割同时给予每日第二次剂量1 g。依从性以每位患者接受的初始规定剂量的百分比来估计。记录主要副作用。

结果

共调查了1049例患者。尼莫唑的耐受性尚可:58%的患者接受了全部规定的总剂量。恶心和呕吐是主要主诉:在因已知副作用而减少剂量的260例患者中,(87%)是由于恶心/呕吐。治疗中断时所有副作用均停止,未观察到严重或长期副作用。女性患者更有可能减少剂量(比值比2.02;95%置信区间1.50 - 2.70),且更易出现恶心/呕吐。70岁以上患者更有可能减少剂量。与接受1100 - 1300 mg/m²的患者相比,接受剂量低于1100 mg/m²的患者减少剂量(比值比0.58;置信区间0.44 - 0.78)以及出现恶心/呕吐的可能性显著更低。接受加速放化疗的患者组耐受性也较差(比值比1.70;置信区间1.20 - 2.50),且与恶心/呕吐的关联更强(比值比2.09;置信区间1.40 - 3.10)。

结论

尼莫唑的依从性尚可,急性毒性可耐受,但无持续性或晚期毒性。它可与化疗及不同的放疗分割方案联合使用。

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