Leblanc B, Duclos A J, Bénard F, Valiquette L, Paquin J M, Lapointe S, Mauffette F, Pharand D, Faucher R, Drouin G, Perreault J P
CHUM - Campus St-Luc, Université de Montréal, Québec.
Can J Urol. 2000 Feb;7(1):944-8.
OBJECTIVE: To review the long-term follow-up, in terms of recurrence and progression, of transitional cell carcinoma of the bladder treated with intravesical BCG with the following indications: CIS, Ta and T1. MATERIALS AND METHODS: Ninety-two patients who had received complete course of BCG between 1987 and 1993 were included in the study and followed for an average of 59 months (range 12 to 102). RESULTS: The recurrence and progression were looked at. Patients treated with BCG for Carcinoma in situ, 11 of 19 (53%) remained tumor-free after 1 or 2 courses of BCG for the duration of the follow-up (mean 4.9 years, range 1.5 to 8.5 years). For patients treated for recurring tumors, 17 of 50 (34%) had no recurrences after 1 or 2 courses of BCG with the same follow-up. When facing multiple tumors, 10 of 23 (43%) patients did not experience recurrences. Therefore, in the 92 patients treated, 38 presented no recurrences after 1 or 2 courses of BCG, for a success rate of 41%. In terms of progression, of the 19 patients treated with BCG for CIS, 4 (21%) went on to develop muscle invasive disease. Of the 50 patients treated for recurrent tumors, 2 (4%) eventually developed lamina propria invasion (initial lesion was a Ta tumor), 4 (8%) carcinoma in situ and 7 (14%) muscle invasive disease, for an overall progression rate of 26% in this group. Of the 25 patients treated for multiple tumors, 1 (4%) developed CIS and 3 (12%) presented with muscle invasive disease, for an overall progression rate of 16% for the duration of the follow-up. Therefore, 21 of 92 (23%) patients had progression of their disease following BCG therapy. No prognostic factors for recurrence or progression could be identified in these tumors. CONCLUSION: When indications warrant its use, BCG is effective in reducing recurrences and limiting progression in TCC of the bladder. Recurrence within 2 years of treatment is, however, a sign of poor prognosis and other therapeutic options should be sought.
目的:回顾膀胱灌注卡介苗治疗膀胱移行细胞癌(CIS、Ta和T1期)后的长期随访情况,重点关注复发和进展情况。 材料与方法:本研究纳入了1987年至1993年间接受卡介苗完整疗程治疗的92例患者,平均随访59个月(范围12至102个月)。 结果:观察了复发和进展情况。原位癌患者接受卡介苗治疗后,19例中有11例(53%)在1或2个疗程的卡介苗治疗后至随访结束(平均4.9年,范围1.5至8.5年)期间无肿瘤复发。复发性肿瘤患者中,50例中有17例(34%)在相同随访期内接受1或2个疗程卡介苗治疗后无复发。对于多发肿瘤患者,23例中有10例(43%)未出现复发。因此,在接受治疗的92例患者中,38例在1或2个疗程卡介苗治疗后未复发,成功率为41%。在进展方面,19例原位癌接受卡介苗治疗的患者中,4例(21%)进展为肌层浸润性疾病。50例复发性肿瘤患者中,2例(4%)最终出现固有层浸润(初始病变为Ta肿瘤),4例(8%)出现原位癌,7例(14%)出现肌层浸润性疾病,该组总体进展率为26%。25例多发肿瘤患者中,1例(4%)出现原位癌,3例(12%)出现肌层浸润性疾病,随访期间总体进展率为16%。因此,92例患者中有21例(23%)在卡介苗治疗后病情进展。在这些肿瘤中未发现复发或进展的预后因素。 结论:在适应证允许时,卡介苗可有效减少膀胱移行细胞癌的复发并限制其进展。然而,治疗后2年内复发是预后不良的迹象,应寻求其他治疗选择。
World J Urol. 2010-11-28