Thomas Derek E, Kaimakliotis Hristos Z, Rice Kevin R, Pereira Jose A, Johnston Paul, Moore Marietta L, Reed Angela, Cregar Dylan M, Franklin Cindy, Loman Rhoda L, Koch Michael O, Bihrle Richard, Foster Richard S, Masterson Timothy A, Gardner Thomas A, Sundaram Chandru P, Powell Charles R, Beck Stephen D W, Grignon David J, Cheng Liang, Albany Costantine, Hahn Noah M
Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN; Department of Urology, Indiana University School of Medicine, Indianapolis, IN.
Clin Genitourin Cancer. 2017 Aug;15(4):479-486. doi: 10.1016/j.clgc.2016.11.009. Epub 2016 Nov 30.
Carcinoma in situ (CIS) is a poor prognostic finding in urothelial carcinoma. However, its significance in muscle-invasive urothelial carcinoma (MIUC) treated with neoadjuvant chemotherapy (NAC) is uncertain. We assessed the effect of CIS found in pretreatment transurethral resection of bladder tumor (TURBT) biopsies on the pathologic and clinical outcomes.
Subjects with MIUC treated with NAC before cystectomy were identified. The pathologic complete response (pCR) rates stratified by TURBT CIS status were compared. The secondary analyses included tumor response, progression-free survival (PFS), overall survival (OS), and an exploratory post hoc analysis of patients with pathologic CIS only (pTisN0) at cystectomy.
A total of 137 patients with MIUC were identified. TURBT CIS was noted in 30.7% of the patients. The absence of TURBT CIS was associated with a significantly increased pCR rate (23.2% vs. 9.5%; odds ratio, 4.08; 95% confidence interval, 1.19-13.98; P = .025). Stage pTisN0 disease was observed in 19.0% of the TURBT CIS patients. TURBT CIS status did not significantly affect the PFS or OS outcomes. Post hoc analysis of the pTisN0 patients revealed prolonged median PFS (104.5 vs. 139.9 months; P = .055) and OS (104.5 vs. 152.3 months; P = .091) outcomes similar to those for the pCR patients.
The absence of CIS on pretreatment TURBT in patients with MIUC undergoing NAC was associated with increased pCR rates, with no observed differences in PFS or OS. Isolated CIS at cystectomy was frequently observed, with lengthy PFS and OS durations similar to those for pCR patients. Further studies aimed at understanding the biology and clinical effect of CIS in MIUC are warranted.
原位癌(CIS)是尿路上皮癌预后不良的表现。然而,其在接受新辅助化疗(NAC)的肌层浸润性尿路上皮癌(MIUC)中的意义尚不确定。我们评估了在膀胱肿瘤经尿道切除术(TURBT)活检中发现的原位癌对病理和临床结果的影响。
确定接受膀胱切除术前行NAC治疗的MIUC患者。比较按TURBT原位癌状态分层的病理完全缓解(pCR)率。二次分析包括肿瘤反应、无进展生存期(PFS)、总生存期(OS),以及对膀胱切除术中仅存在病理原位癌(pTisN0)患者的探索性事后分析。
共确定137例MIUC患者。30.7%的患者在TURBT中发现原位癌。未发现TURBT原位癌与pCR率显著升高相关(23.2%对9.5%;优势比,4.08;95%置信区间,1.19 - 13.98;P = 0.025)。19.0%的TURBT原位癌患者观察到pTisN0期疾病。TURBT原位癌状态对PFS或OS结果无显著影响。对pTisN0患者的事后分析显示,中位PFS(104.5对139.9个月;P = 0.055)和OS(104.5对152.3个月;P = 0.091)结果与pCR患者相似。
接受NAC的MIUC患者术前TURBT未发现原位癌与pCR率升高相关,在PFS或OS方面未观察到差异。膀胱切除术中孤立性原位癌常见,其PFS和OS持续时间与pCR患者相似。有必要进一步开展研究以了解MIUC中原位癌的生物学特性和临床效应。