Validation of lymphovascular invasion is an independent prognostic factor for biochemical recurrence after radical prostatectomy

被引:13
|
作者
Fajkovic, Harun [1 ]
Mathieu, Romain [1 ,2 ]
Lucca, Ilaria [1 ,3 ]
Hiess, Manuela [1 ]
Huebner, Nicolai [1 ]
Al Awamlh, Bashir Al Hussein [4 ]
Lee, Richard [4 ]
Briganti, Alberto [5 ]
Karakiewicz, Pierre [6 ]
Lotan, Yair [7 ]
Roupret, Morgan [8 ]
Rink, Michael [9 ]
Kluth, Luis [9 ]
Loidl, Wolfgang [10 ]
Seitz, Christian [1 ]
Klatte, Tobias [1 ]
Kramer, Gero [1 ]
Susani, Martin [11 ]
Shariat, Shahrokh F. [1 ,3 ,7 ]
机构
[1] Med Univ Vienna, Vienna Gen Hosp, Ctr Comprehens Canc, Dept Urol, Vienna, Austria
[2] Rennes Univ Hosp, Dept Urol, Rennes, France
[3] CHU Vaudois, Dept Urol, CH-1011 Lausanne, Switzerland
[4] Cornell Univ, Dept Urol, Weill Med Coll, New York Presbyterian Hosp, New York, NY 10021 USA
[5] Ist Sci San Raffaele, Dept Urol, Urol Res Inst, I-20132 Milan, Italy
[6] Univ Montreal, Ctr Hlth, Canc Prognost & Hlth Outcomes Unit, Montreal, PQ, Canada
[7] Univ Texas SW Med Ctr Dallas, Dept Urol, Dallas, TX 75390 USA
[8] Hop La Pitie Salpetriere, Dept Urol, Paris, France
[9] Univ Med Ctr Hamburg Eppendorf, Dept Urol, Hamburg, Germany
[10] St Vincents Hosp, Dept Urol, Linz, Austria
[11] Med Univ Vienna, Dept Pathol, Vienna, Austria
关键词
Localized prostate cancer; Biochemical recurrence; Lymphovascular invasion; Radical prostatectomy; PATHOLOGICAL FEATURE; SPECIMENS; CANCER; DISEASE; RADIOTHERAPY; PROGRESSION; CYSTECTOMY; PREDICTOR; SURVIVAL; IMPACT;
D O I
10.1016/j.urolonc.2015.10.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To validate the impact of lymphovascular invasion (LVI) on biochemical recurrence (BCR) in patients treated with radical prostatectomy (RP) in a large multiinstitutional cohort. Material and methods: Retrospective data from 6,678 patients treated with a RP and bilateral lymphadenectomy for prostate cancer (PC) from 8 centers were collected. The primary endpoint was BCR. Results: Overall, 767 patients (11.5%) had LVI. Patients with LVI had significantly higher Gleason scores (P = 0.01). After a median follow-up of 28 months (interquartile range: 21-44), patients with LVI had a 1.66 fold increased risk of BCR (P < 0.001). The 1-, 2- and 5-year biochemical recurrence-free survival probabilities for LVI vs. no LVI were 94% vs. 97%, 91% vs. 94%, and 76% vs. 84%, respectively. On multivariable analysis that adjusted for the effects of established prognostic factors, LVI was an independent predictor of BCR (hazard ratio = 1.42, P < 0.001). Adding LVI to a multivariable base model increased the discrimination by a small but significant margin (+0.2%, P = 0.0005). In subgroup analyses, LVI remained an independent predictor for BCR in patients with worse pathological features. Conclusions: About 10% of patients with localized PC have LVI on their RP specimen. We confirm that LVI is associated with features of biologic aggressive PC such as high Gleason grade and BCR after RP. Adverse further studies with strict definitions of LVI and longer follow-up periods are needed to determine the prognostic and predictive utility of LVI in the management of PC. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:233.e1 / 233.e6
页数:6
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