1. The Impact of Histological Variants on Oncological Outcomes After Surgical Resection of a Nonmetastatic Renal Cell Carcinoma with Tumor Thrombus: A Multi-institutional Study
- Author
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Raphael Fleury, Théophile Bertail, Karim Bensalah, Jean-Christophe Bernhard, Francois Audenet, Thibaut Waeckel, Bastien Parier, Cécile Champy, Jonathan Olivier, Nicolas Doumerc, Thibault Tricard, Nicolas Branger, Franck Bruyere, Paul Neuville, Louis Surlemont, Jean Alexandre Long, Alexis Fontenil, Maxime Vallee, Morgan Roupret, Romain Boissier, Jean Jacques Patard, Mathieu Durand, Idir Ouzaid, Benjamin Rouget, Xavier Durand, Charlotte Joncour, Olivier Belas, Florie Denise Gomez, Pierre Bigot, and Zine-Eddine Khene
- Subjects
Kidney cancer ,Thrombus ,Renal cell carcinoma ,Histological variants ,Prognosis ,Recurrence ,Diseases of the genitourinary system. Urology ,RC870-923 ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Background: There is no definitive evidence of the prognosis impact of histological variants (HVs) in patients who undergo surgical resection of a nonmetastatic renal cell carcinoma (nm-RCC) with venous tumor thrombus (TT). Objective: To investigate the impact of HVs on the prognosis of patients with nm-RCC with TT after radical surgery. Design, setting, and participants: Patients who underwent radical nephrectomy with the removal of the venous TT for an nm-RCC were included in a retrospective study. Outcome measurements and statistical analysis: Three groups were identified: clear cell (ccRCC), papillary (pRCC), and chromophobe (chRCC) RCC. The primary outcome measures (disease-free and overall survival [OS]) were assessed using the Kaplan-Meier method and compared using the log-rank test. Univariate and multivariate Cox proportional hazard models were used to study the impact of HVs on survival. Results and limitations: A total of 873 patients were included. The histological subtypes were distributed as follows: ccRCC in 780 cases, pRCC in 58 cases, and chRCC in 35 cases. At the time of data analysis, 612 patients were recurrence free and 228 had died. A survival analysis revealed significant differences in both OS and recurrence-free survival across histological subtypes, with the poorest outcomes observed in pRCC patients (p
- Published
- 2024
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