Grimbergen M C M, van Swol C F P, Jonges T G N, Boon T A, van Moorselaar R J A
Department of Biomedical Engineering, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA Utrecht, The Netherlands.
Eur Urol. 2003 Jul;44(1):51-6. doi: 10.1016/s0302-2838(03)00210-0.
Photodynamic diagnosis (PDD) for the detection of bladder cancer has become a diagnostic tool in several hospitals. Several studies have reported different rates of false positive biopsies using 5-aminolevulinic acid induced fluorescence. In this study we evaluated the effect of previous intravesical therapy on the false positive biopsy rate.
Two hours prior to endoscopy 1.5g ALA dissolved in 50ml 1.4% NaHCO(3) solution was instilled intravesically. For fluorescence excitation a blue light source (D-light, Karl Storz) was used. Under white and fluorescence light guidance, tumor locations were recorded, cold cup biopsies were taken and tumors were resected. Patients were divided into 3 groups, last intravesical therapy (IVT) less than 6 months prior to PDD, last IVT longer than 6 months before PDD and no previous IVT.
In total 917 biopsies were taken in 249 procedures of fluorescent and non-fluorescent areas. White light endoscopy revealed 270 and PDD 378 of in total 390 tumors, resulting in a sensitivity of 97% and specificity of 49% for PDD. Pathologic evaluation considered 270 fluorescent biopsies as false positive. The rate of false positive biopsies was 25.7% in the group No IVT, 30.6% in the group PDD-IVT >6 months, whereas in the group "within 6 months after intravesical therapy" the rate was 39.6% (p<0.025). When premalignant lesions such as dysplasia II are considered tumor the difference between the groups is even more significant (p<0.001).
The procedure has a high sensitivity for superficial bladder cancer and decreases the number of overlooked lesions. Recent intravesical therapy results in significantly more false positive fluorescent biopsies. Since patient outcome might predominantly be determined by the early detection and subsequent treatment of (pre)malignant tissue we suggest that PDD is justified even shortly after intravesical therapy.
光动力诊断(PDD)用于膀胱癌检测已成为多家医院的一种诊断工具。多项研究报告了使用5-氨基酮戊酸诱导荧光进行活检时不同的假阳性率。在本研究中,我们评估了既往膀胱内治疗对活检假阳性率的影响。
在内镜检查前两小时,将1.5g 5-氨基酮戊酸溶解于50ml 1.4%碳酸氢钠溶液中膀胱内灌注。使用蓝光光源(D-light,Karl Storz)进行荧光激发。在白光和荧光引导下,记录肿瘤位置,进行冷杯活检并切除肿瘤。患者分为3组,PDD前最后一次膀胱内治疗(IVT)少于6个月,PDD前最后一次IVT超过6个月,以及既往无IVT。
在249例荧光和非荧光区域的操作中,共进行了917次活检。白光内镜检查发现390个肿瘤中的270个,PDD发现378个,PDD的敏感性为97%,特异性为49%。病理评估将270次荧光活检视为假阳性。无IVT组的活检假阳性率为25.7%,PDD-IVT>6个月组为30.6%,而“膀胱内治疗后6个月内”组的假阳性率为39.6%(p<0.025)。当将发育异常II等癌前病变视为肿瘤时,各组之间的差异更为显著(p<0.001)。
该方法对浅表性膀胱癌具有高敏感性,减少了漏诊病变的数量。近期膀胱内治疗导致荧光活检假阳性显著增多。由于患者的预后可能主要取决于(癌)前组织的早期检测和后续治疗,我们建议即使在膀胱内治疗后不久,PDD也是合理的。