Lymphovascular Invasion Predicts Clinical Outcomes in Patients With Node-Negative Upper Tract Urothelial Carcinoma

American Society of Clinical Oncology (ASCO) - Tập 27 Số 4 - Trang 612-618 - 2009
Eiji Kikuchi1, Vitaly Margulis1, Pierre I. Karakiewicz1, Marco Roscigno1, Shuji Mikami1, Yair Lotan1, Mesut Remzi1, Christian Bolenz1, Cord Langner1, Alon Z. Weizer1, Francesco Montorsi1, Karim Bensalah1, Theresa M. Koppie1, Mario I. Fernández1, Jay D. Raman1, Wassim Kassouf1, Christopher G. Wood1, Nazareno Suardi1, Mototsugu Oya1, Shahrokh F. Shariat1
1From Keio University School of Medicine, Tokyo, Japan; The University of Texas M. D. Anderson Cancer Center, Houston; University of Texas Southwestern Dallas, Dallas, TX; University of Michigan, Ann Arbor, MI; University of California Davis, Sacramento, CA; Cornell University, New York, NY; University of Montreal; McGill University, Montreal, Quebec, Canada; Vita-Salute University, Milan, Italy; University of Vienna, Vienna; Medical University Graz, Graz, Austria; University Medical Center Mannheim,...

Tóm tắt

Purpose To assess the association of lymphovascular invasion (LVI) with cancer recurrence and survival in a large international series of patients treated with radical nephroureterectomy (RNU) for upper urinary tract urothelial carcinoma (UTUC). Patients and Methods Data were collected on 1,453 patients treated with RNU at 13 academic centers and combined into a relational database. Pathologic slides were rereviewed by genitourinary pathologists according to strict criteria. LVI was defined as presence of tumor cells within an endothelium-lined space. Results LVI was observed in 349 patients (24%). Proportion of LVI increased with advancing tumor stage, high tumor grade, presence of tumor necrosis, sessile tumor architecture, and presence of lymph node metastasis (all P < .001). LVI was an independent predictor of disease recurrence and survival (P < .001 for both). Addition of LVI to the base model (comprising pathologic stage, grade, and lymph node status) marginally improved its predictive accuracy for both disease recurrence and survival (1.1%, P = .03; and 1.7%, P < .001, respectively). In patients with negative lymph nodes and those in whom a lymphadenectomy was not performed (n = 1,313), addition of LVI to the base model improved the predictive accuracy of the base model for both disease recurrence and survival by 3% (P < .001 for both). In contrast, LVI was not associated with disease recurrence or survival in node-positive patients (n = 140). Conclusion LVI was an independent predictor of clinical outcomes in nonmetastatic patients who underwent RNU for UTUC. Assessment of LVI may help identify patients who could benefit from multimodal therapy after RNU. After confirmation, LVI should be included in staging of UTUC.

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