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卡介苗治疗膀胱原位癌后侵袭性癌的尿道复发

[Urethral recurrence of invasive carcinoma following BCG treatment for bladder Ca in situ].

作者信息

Ruoppolo M, Gozo M, Milesi R, Spina R, Fragapane G

机构信息

UO Urologia, Azienda Ospedaliera Ospedale Treviglio-Caravaggio (Bergamo), Italy.

出版信息

Urologia. 2010 Oct-Dec;77 Suppl 17:72-7.

Abstract

CIS is a flat, high-grade, non-invasive microscopic urothelial carcinoma. It is considered a precursor of invasive bladder cancer. CIS is classified as primary, secondary or concurrent, when occurred as isolated CIS without cuncurrent papillary tumors, or detected during the follow-up of patients with a previous papillary tumor, or finally in the presence of bladder neoplasm. BCG is widely established as the treatment of choice for CIS with a success rate of approximately 70%. BCG reduces the risk of progression of CIS into invasive carcinoma in 30 to 50% of cases. Direct and prolonged contact between the urothelium and BCG is a prerequisite for successful therapy. Discovery of CIS in the prostatic or membranous urethra represents an ominous sign. CIS may be present only in the epithelial lining of the prostatic urethra or in the ducts, or in the worst case it may be found in the prostatic tissue stroma. Urethral involvement by CIS is at high risk of tumor progression and development of metastases due to reduced thickness of lamina propria and absence of muscolaris mucosa. 83 patients, enrolled from 1/1996 to 12/2005 at our urological department with CIS: primary (focal and multifocal) in 25, secondary in 7 and cuncurrent in 51 (associated with T1bG3 cancer in 37 cases), and urethral CIS in 5 and conservatively treated by TUR and intravescical instillations of BCG, 4 developed afterwords only invasive cancer of the urethra in the absence of bladder involvement. In 2 cases cancer arised from the prostatic fossa after TURP, in 1 from membranous urethra and in the last from prostatic ducts. Among the 4 patients, 3 were treated by cystoprostatourethrectomy and Platinum-based chemotherapy, 1 refused surgical treatment. Two patients died for disseminated disease. 1 patient is alive at 60-month's follow-up. In the last patient cancer relapsed at 36-month's follow-up. We conclude that prostatic/urethral involvement during follow-up after successful intravesical treatment with BCG in CIS represents a high risk of developing invasive and incontrolled cancer. A careful watch is recommended in these patients.

摘要

原位癌是一种扁平的、高级别、非侵袭性的微观尿路上皮癌。它被认为是浸润性膀胱癌的前驱病变。原位癌可分为原发性、继发性或同时性,分别指孤立出现且无并发乳头状肿瘤的原位癌、在既往有乳头状肿瘤患者的随访过程中检测到的原位癌,或最终在存在膀胱肿瘤的情况下出现的原位癌。卡介苗(BCG)已被广泛确立为原位癌的首选治疗方法,成功率约为70%。卡介苗可使30%至50%的原位癌病例降低进展为浸润性癌的风险。尿路上皮与卡介苗的直接和长时间接触是成功治疗的前提条件。在前列腺或膜部尿道发现原位癌是一个不祥之兆。原位癌可能仅存在于前列腺尿道的上皮内衬或导管中,最坏的情况是在前列腺组织基质中发现。由于固有层厚度减小且缺乏黏膜肌层,原位癌累及尿道时肿瘤进展和发生转移的风险很高。1996年1月至2005年12月期间,我们泌尿外科收治了83例原位癌患者:原发性(局灶性和多灶性)25例,继发性7例,同时性51例(37例与T1bG3癌相关),5例为尿道原位癌,均接受经尿道切除术(TUR)和膀胱内灌注卡介苗保守治疗,其中4例后来仅出现尿道浸润性癌,而无膀胱受累。2例在经尿道前列腺电切术(TURP)后前列腺窝发生癌症,1例在膜部尿道发生癌症,最后1例在前列腺导管发生癌症。在这4例患者中,3例接受了膀胱前列腺尿道切除术和铂类化疗,1例拒绝手术治疗。2例患者因疾病播散死亡。1例患者在60个月的随访中存活。最后1例患者在36个月的随访中癌症复发。我们得出结论,卡介苗膀胱内成功治疗原位癌后的随访期间,前列腺/尿道受累意味着发生浸润性和失控性癌症的高风险。建议对这些患者进行密切观察。

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