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5-氨基酮戊酸诱导荧光膀胱镜检测膀胱癌及其临床转归:一项多中心、随机、双盲、安慰剂对照研究。

Detection and clinical outcome of urinary bladder cancer with 5-aminolevulinic acid-induced fluorescence cystoscopy : A multicenter randomized, double-blind, placebo-controlled trial.

机构信息

Medical Center of Eberhard Karls University, Department of Urology, Tübingen, Germany.

出版信息

Cancer. 2011 Mar 1;117(5):938-47. doi: 10.1002/cncr.25523. Epub 2010 Nov 8.

DOI:10.1002/cncr.25523
PMID:21351082
Abstract

BACKGROUND

The medical community lacks results from prospective controlled multicenter studies of the diagnostic efficacy of 5-aminolevulinic acid (5-ALA) cystoscopy on tumor recurrence in patients with superficial bladder tumors.

METHODS

A prospective randomized, double-blind, placebo-controlled study was conducted in 370 patients with nonmuscle-invasive urinary bladder carcinoma who received either 5-ALA (n = 187) or a placebo (n = 183) intravesically before cystoscopy. Each group underwent cystoscopy under visible white light and under fluorescent light followed by transurethral tumor resection. The primary study objective was to evaluate the 12-month recurrence-free survival.

RESULTS

Slightly more patients with tumors were detected by using 5-ALA than by using the placebo (88.5% vs 84.7%). The mean numbers of tumor specimens per patient were 1.8 (5-ALA) and 1.6 (placebo). Intrapatient comparison of fluorescent light versus white light cystoscopy in patients randomized to receive 5-ALA showed a higher tumor detection rate with fluorescent light than with white light cystoscopy. In patients receiving 5-ALA cystoscopy, the percentage of lesions that would not have been detected in these patients by white light cystoscopy ranged between 10.9% (pT1) and 55.9% (atypia). Progression-free survival was 89.4% (5-ALA) and 89.0% (placebo) (P = .9101), and recurrence-free survival 12 months after tumor resection was 64.0% (5-ALA) and 72.8% (placebo) (P = .2216).

CONCLUSIONS

In comparison to the placebo, 5-ALA cystoscopy did not increase the rates of recurrence-free or progression-free survival 12 months after tumor resection. Although more tumors per patient were detected in the 5-ALA group, the higher detection rate did not translate into differences in long-term outcome.

摘要

背景

医学领域缺乏关于 5-氨基酮戊酸(5-ALA)膀胱镜检查对浅表膀胱癌患者肿瘤复发的诊断疗效的前瞻性对照多中心研究结果。

方法

对 370 例非肌层浸润性膀胱癌患者进行了一项前瞻性随机、双盲、安慰剂对照研究,这些患者在膀胱镜检查前分别接受了 5-ALA(n=187)或安慰剂(n=183)腔内给药。两组均在可见白光和荧光光下进行膀胱镜检查,然后行经尿道肿瘤切除术。主要研究目的是评估 12 个月无复发生存率。

结果

使用 5-ALA 检测到的肿瘤患者略多于使用安慰剂(88.5% vs 84.7%)。每位患者的肿瘤标本平均数量为 1.8(5-ALA)和 1.6(安慰剂)。在接受 5-ALA 膀胱镜检查的患者中,荧光光与白光膀胱镜检查的患者比较,荧光光下肿瘤检出率更高。在接受 5-ALA 膀胱镜检查的患者中,白光膀胱镜检查可能会漏诊的病变比例在 10.9%(pT1)至 55.9%(非典型增生)之间。无进展生存率为 89.4%(5-ALA)和 89.0%(安慰剂)(P=0.9101),肿瘤切除后 12 个月无复发生存率为 64.0%(5-ALA)和 72.8%(安慰剂)(P=0.2216)。

结论

与安慰剂相比,肿瘤切除后 12 个月时,5-ALA 膀胱镜检查并未增加无复发生存率或无进展生存率。尽管 5-ALA 组每个患者检测到的肿瘤数量更多,但更高的检出率并未转化为长期结局的差异。

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