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用于治疗头颈部癌症患者同期放化疗后放射性黏膜炎相关疼痛综合征的加巴喷丁。

Gabapentin for the treatment of pain syndrome related to radiation-induced mucositis in patients with head and neck cancer treated with concurrent chemoradiotherapy.

机构信息

Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

出版信息

Cancer. 2010 Sep 1;116(17):4206-13. doi: 10.1002/cncr.25274.

Abstract

BACKGROUND

This retrospective study evaluated the efficacy of gabapentin for the treatment of pain syndromes related to radiation-induced mucositis in patients with head and neck cancers treated with concurrent chemoradiation.

METHODS

Data from 42 patients with head and neck malignancies treated with concurrent chemoradiotherapy using an intensity-modulated radiotherapy technique were analyzed. Gabapentin was initiated in the second week of radiotherapy. Opiates were prescribed in addition to gabapentin as clinically indicated to obtain adequate pain control.

RESULTS

At a median dose of 2700 mg/day of gabapentin, only 33% and 55% of patients required additional low-dose narcotic medications for pain control during the third and fourth week of treatment, respectively, despite exhibiting a grade 2 or higher mucositis in 71% and 86% of the patients, respectively. Furthermore, during the last weeks of treatment, 71% of the patients required additional low-dose opiates for adequate pain control, despite the presence of grade 2 or higher mucositis in 95% and 100% of patients at Weeks 5 and 6, respectively. Only 1 patient had a treatment-related interruption of >3 days during chemoradiotherapy.

CONCLUSIONS

Gabapentin appears to be promising in reducing the need for high total doses of opioids and avoiding unplanned treatment interruptions for patients with head and neck malignancies treated with concurrent chemoradiotherapy and should be further evaluated prospectively in controlled clinical trials.

摘要

背景

本回顾性研究评估了加巴喷丁治疗头颈部癌症患者同期放化疗后放射性黏膜炎相关疼痛综合征的疗效。

方法

分析了 42 例采用调强放疗技术同期放化疗的头颈部恶性肿瘤患者的数据。在放射治疗的第二周开始使用加巴喷丁。根据临床需要,除加巴喷丁外还开了阿片类药物,以获得充分的疼痛控制。

结果

在中位数剂量为 2700 mg/天的加巴喷丁治疗下,尽管分别有 71%和 86%的患者在第 3 周和第 4 周出现 2 级或更高的黏膜炎,但仍分别有 33%和 55%的患者需要额外使用低剂量的麻醉性药物来控制疼痛。此外,在治疗的最后几周,尽管分别有 95%和 100%的患者在第 5 周和第 6 周出现 2 级或更高的黏膜炎,但仍有 71%的患者需要额外使用低剂量的阿片类药物来获得充分的疼痛控制。只有 1 例患者在同期放化疗期间因治疗相关原因中断治疗>3 天。

结论

加巴喷丁似乎可以减少头颈部恶性肿瘤患者同期放化疗后对高总剂量阿片类药物的需求,并避免因黏膜炎而计划外中断治疗,应在前瞻性对照临床试验中进一步评估。

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