Oncotarget

Research Papers:

High competing risks minimize real-world utility of adjuvant targeted therapy in renal cell carcinoma: a population-based analysis

Thenappan Chandrasekar _, Zachary Klaassen, Hanan Goldberg, Rashid K. Sayyid and Neil E. Fleshner

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Oncotarget. 2018; 9:16731-16743. https://doi.org/10.18632/oncotarget.24675

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Abstract

Thenappan Chandrasekar1, Zachary Klaassen1, Hanan Goldberg1, Rashid K. Sayyid1, Girish S. Kulkarni1 and Neil E. Fleshner1

1Department of Surgical Oncology, Division of Urology, University Health Network, University of Toronto, Ontario, Canada

Correspondence to:

Thenappan Chandrasekar, email: thenappan.chandrasekar@gmail.com

Keywords: carcinoma, renal cell; neoplasm metastasis; drug therapy; survival; mortality

Received: August 29, 2017     Accepted: February 26, 2018    Published: March 30, 2018

ABSTRACT

Objective: To utilize a population-based approach to address the role of adjuvant TT in the management of RCC.

Methods: Patients with RCC (2006-2013) in the SEER database were stratified by metastatic disease at the time of diagnosis (cM0/cM1). cM0 patients following surgical excision were stratified into low and high-risk (ASSURE and S-TRAC criteria). Multivariable analyses performed to identify predictors of TT receipt; Fine and Gray competing risks analyses used to identify predictors of cancer-specific mortality (CSM). Subset analyses included patients with clear cell histology and high-risk cM0. Survival analyses were used to evaluate overall survival (OS) and cancer-specific survival (CSS) for all cohorts, stratified on TT receipt.

Results: 79,926 patients included (71,682 cM0, 8,244 cM1); median follow-up for the entire cohort was 40.1 months. Of 31,453 patients with histologic grade data, 18,328 and 13,125 were low- and high-risk cM0, respectively. TT utilization in cM1 patients peaked at 50.6% and was associated with reduced CSM (HR 0.73, p<0.01). In contrast, TT utilization (presumed salvage therapy) never exceeded 2.2% in the entire cM0 cohort and 3.5% in the high-risk cM0 cohort. On competing risks analysis, TT receipt was associated with increased CSM in all cohorts.

Conclusion: When compared to the cM1 patients, TT receipt in cM0 patients does not provide any cancer-specific survival benefit, even in the small percentage of patients that eventually progress to metastatic disease. Competing risks mortality further limit any potential benefit in this population. Based on current evidence, adjuvant TT cannot be recommended for RCC patients.


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