Implications of micropapillary urothelial carcinoma variant on prognosis following radical cystectomy: A multi-institutional investigation

被引:20
|
作者
Mitra, Anirban P. [1 ]
Fairey, Adrian S. [2 ]
Skinner, Eila C. [3 ]
Boorjian, Stephen A. [4 ]
Frank, Igor [4 ]
Schoenberg, Mark P. [5 ,6 ]
Bivalacqua, Trinity J. [7 ]
Hyndman, M. Eric [8 ]
Reese, Adam C. [9 ]
Steinberg, Gary D. [10 ]
Large, Michael C. [11 ]
Hulsbergen-van de Kaa, Christina A. [12 ]
Bruins, Harman M. [13 ]
Daneshmand, Siamak [1 ]
机构
[1] Univ Southern Calif, Inst Urol, Los Angeles, CA 90007 USA
[2] Univ Alberta, Div Urol, Dept Surg, Edmonton, AB, Canada
[3] Stanford Univ, Dept Urol, Stanford, CA 94305 USA
[4] Mayo Clin, Dept Urol, Rochester, MN USA
[5] Albert Einstein Coll Med, Dept Urol, Bronx, NY 10467 USA
[6] Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USA
[7] Johns Hopkins Univ, James Buchanan Brady Urol Inst, Baltimore, MD USA
[8] Southern Alberta Inst Urol, Calgary, AB, Canada
[9] Temple Univ, Dept Urol, Philadelphia, PA 19122 USA
[10] Univ Chicago, Dept Surg, Sect Urol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[11] Urol Indiana, Indianapolis, IN USA
[12] Radboud Univ Nijmegen, Dept Pathol, Med Ctr, Nijmegen, Netherlands
[13] Radboud Univ Nijmegen, Dept Urol, Med Ctr, Nijmegen, Netherlands
关键词
UC; urothelial carcinoma; MUC; micropapillary urothelial carcinoma; RFS; recurrence-free survival; OS; overall survival; TRANSITIONAL-CELL CARCINOMA; BLADDER-CANCER; URINARY-BLADDER; NEOADJUVANT CHEMOTHERAPY; DIFFERENTIATION; MANAGEMENT; OUTCOMES; PATTERN; IMPACT;
D O I
10.1016/j.urolonc.2018.10.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the association of micropapillary urothelial carcinoma (MUC) variant histology with bladder cancer outcomes after radical cystectomy. Materials and Methods: Information on MUC patients treated with radical cystectomy was obtained from five academic centers. Data on 1,497 patients were assembled in a relational database. Tumor histology was categorized as urothelial carcinoma without any histological variants (UC; n = 1,346) or MUC (n = 151). Univariable and multivariable models were used to analyze associations with recurrence-free (RFS) and overall (OS) survival. Results: Median follow-up was 10.0 and 7.8 years for the UC and MUC groups, respectively. No significant differences were noted between UC and MUC groups with regard to age, gender, clinical disease stage, and administration of neoadjuvant and adjuvant chemotherapy (all, P = 0.10). When compared with UC, presence of MUC was associated with higher pathologic stage (organ-confined, 60% vs. 27%; extravesical, 18% vs. 23%; node-positive, 22% vs. 50%; P < 0.01) and lymphovascular invasion (29% vs. 58%; P < 0.01) at cystectomy. In comparison with UC, MUC patients had poorer 5-year RFS (70% vs. 44%; P < 0.01) and OS (61% vs. 38%; P < 0.01). However, on multivariable analysis, tumor histology was not independently associated with the risks of recurrence (P = 0.27) or mortality (P = 0.12). Conclusions: This multi-institutional analysis demonstrated that the presence of MUC was associated with locally advanced disease at radical cystectomy. However, clinical outcomes were comparable to those with pure UC after controlling for standard clinicopathologic predictors. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:48 / 56
页数:9
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