Schwalb M D, Herr H W, Sogani P C, Russo P, Sheinfeld J, Fair W R
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
J Urol. 1994 Aug;152(2 Pt 1):382-7. doi: 10.1016/s0022-5347(17)32744-1.
The pattern of disease recurrence was examined in 75 patients with clinically undetectable positive urinary cytology results following a complete response to intravesical bacillus Calmette-Guerin (BCG) therapy for superficial bladder cancer. A complete response was defined as negative cystoscopy and biopsy findings, urine cytology and flow cytometry (when available) for at least 1 year following therapy. Urinary cytology was positive in the absence of clinical disease at a median of 25 months (range 12 to 96) after BCG administration. Clinically recognizable disease (defined by a positive biopsy or visible papillary tumor) developed at a median of 6 months (range 2 to 60) after positive cytology was detected in 62 patients (83%), while 13 (17%) had persistently positive cytology results without an obvious source at a median of 6 months (range 2 to 29). The bladder was the single most common site of recurrence, with 39 recurrences developing in 36 patients (58%, 3 of whom had recurrent cancer after a complete response to each of 2 separate courses of BCG): 30 (77%) were superficial (stages Ta in 2, Tis in 25, Tis/T1 in 2 and T1 in 1) and 9 (23%) were invasive (stage T2+). Median interval to the detection of bladder recurrence following a positive cytology result was 6 months (range 2 to 50). Upper urinary tract disease developed at a median of 7 months (range 2 to 41) in 11 patients (18%), while 7 (11%) had a prostatic recurrence at a median of 5 months (range 2 to 60). There were 9 synchronous bladder and prostate (5) or upper tract (4) recurrences in 8 patients (13%) at a median of 22 months (range 2 to 40) in the former group and 15.5 months (range 3 to 20) in the latter group. Overall, of 75 sites of recurrence in 62 patients 48 (64%) were in the bladder, 15 (20%) in the upper urinary tract and 12 (16%) in the prostate. High risk patients with superficial bladder cancer who have clinically unconfirmed positive urinary cytology results following a complete response to intravesical BCG therapy require aggressive evaluation of intravesical and extravesical sites to detect the presence of persistent or progressive in situ or invasive disease.
对75例浅表性膀胱癌患者进行了疾病复发模式的研究,这些患者在接受膀胱内卡介苗(BCG)治疗完全缓解后,尿液细胞学检查结果呈临床不可检测的阳性。完全缓解定义为治疗后至少1年膀胱镜检查和活检结果为阴性、尿液细胞学检查和流式细胞术(如有)结果为阴性。卡介苗给药后,尿液细胞学在无临床疾病的情况下呈阳性,中位时间为25个月(范围12至96个月)。62例患者(83%)在检测到尿液细胞学阳性后,临床可识别的疾病(由活检阳性或可见乳头状肿瘤定义)在中位时间6个月(范围2至60个月)出现,而13例患者(17%)在中位时间6个月(范围2至29个月)尿液细胞学结果持续阳性且无明显来源。膀胱是最常见的复发部位,36例患者中有39例复发(58%,其中3例在对2个单独疗程的卡介苗治疗均完全缓解后发生复发性癌症):30例(77%)为浅表性(Ta期2例、Tis期25例、Tis/T1期2例、T1期1例),9例(23%)为浸润性(T2+期)。尿液细胞学阳性结果后检测到膀胱复发的中位间隔时间为6个月(范围2至50个月)。11例患者(18%)上尿路疾病在中位时间7个月(范围2至41个月)出现,7例患者(11%)前列腺复发在中位时间5个月(范围2至60个月)出现。8例患者(13%)有9例膀胱和前列腺(5例)或上尿路(4例)同步复发,前者中位时间为22个月(范围2至40个月),后者为15.5个月(范围3至20个月)。总体而言,62例患者的75个复发部位中,48个(64%)在膀胱,15个(20%)在上尿路,12个(16%)在前列腺。浅表性膀胱癌高危患者在膀胱内卡介苗治疗完全缓解后尿液细胞学检查结果临床未确认阳性,需要对膀胱内和膀胱外部位进行积极评估,以检测是否存在持续性或进展性原位或浸润性疾病。