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氟康唑对头颈部肿瘤放疗患者口腔念珠菌病的预防作用:一项双盲安慰剂对照试验的结果

Effects of fluconazole in the prophylaxis of oropharyngeal candidiasis in patients undergoing radiotherapy for head and neck tumour: results from a double-blind placebo-controlled trial.

作者信息

Corvò R, Amichetti M, Ascarelli A, Arcangeli G, Buffoli A, Cellini N, Cionini L, De Renzis C, Emiliani E, Franchini P, Gabriele P, Gobitti C, Grillo Ruggieri F, Bertoni F, Magrini S M, Marmiroli L, Orsatti M, Panizza G M, Tordiglione M, Ziccarelli L, Gava A, Zorat P L, Ghelfi R, Serra G F, Vitale V

机构信息

University of Genoa, National Cancer Research Institute, Genoa, Italy.

出版信息

Eur J Cancer Care (Engl). 2008 May;17(3):270-7. doi: 10.1111/j.1365-2354.2007.00855.x.

Abstract

Fluconazole is recommended in the prophylaxis of oropharyngeal candidiasis (OPC) in patients undergoing radiotherapy for head-neck tumours; however, the actual effectiveness of fluconazole in this setting remains unclear. Adult patients with cervico-cephalic carcinoma submitted to radical or adjuvant radiotherapy were randomized to 100 mg fluconazole (n = 138) or matched placebo (n = 132) oral suspension once daily from the sixth session of radiotherapy up to the end of treatment. The final analysis of the investigation showed a higher rate of the OPC outbreak-free survival in the fluconazole compared with placebo (P = 0.008 in the log-rank test). The mean time (95% CI) to OPC outbreak was 56 (53-59) days in the fluconazole group and 47 (43-51) days with placebo. The mean duration of radiotherapy was 43.5 and 39.9 days, respectively in the two groups (P = 0.027). Adverse effects were reported in 70.3% of patients in the fluconazole group and in 67.4% with placebo. The results showed prophylaxis with fluconazole given in irradiated patients with head-neck tumours significantly reduces the rate and the time to development of OPC compared with placebo.

摘要

对于接受头颈部肿瘤放疗的患者,推荐使用氟康唑预防口腔念珠菌病(OPC);然而,氟康唑在这种情况下的实际疗效仍不明确。将接受根治性或辅助性放疗的成年头颈癌患者随机分为两组,一组每天口服100毫克氟康唑(n = 138),另一组口服匹配的安慰剂(n = 132),从放疗第六次开始直至治疗结束。该调查的最终分析显示,与安慰剂相比,氟康唑组无OPC爆发存活的比例更高(对数秩检验P = 0.008)。氟康唑组发生OPC爆发的平均时间(95%置信区间)为56(53 - 59)天,安慰剂组为47(43 - 51)天。两组的平均放疗持续时间分别为43.5天和39.9天(P = 0.027)。氟康唑组70.3%的患者报告有不良反应,安慰剂组为67.4%。结果表明,与安慰剂相比,对头颈部肿瘤放疗患者预防性使用氟康唑可显著降低OPC的发生率和发生时间。

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