University of Calgary, Calgary, AB, Canada
Bimal Bhindi , Jeffrey Graham , Connor Wells , Frede Donskov , Felice Pasini , Jae-Lyun Lee , Naveen S. Basappa , Aaron Richard Hansen , Lori Wood , Christian K. Kollmannsberger , Ravindran Kanesvaran , Takeshi Yuasa , D. Scott Ernst , Sandy Srinivas , Brian I. Rini , I. Alex Bowman , Sumanta K. Pal , Toni K. Choueiri , Daniel Yick Chin Heng
Background: While the CARMENA trial prompts more caution with upfront cytoreductive nephrectomy (CN) in patients with metastatic renal cell carcinoma (mRCC), 17% of patients in the sunitinib alone arm underwent deferred CN (dCN). Upfront systemic therapy has been proposed as a potential litmus test to identify patients suitable for CN, but data on outcomes are limited. We sought to characterize outcomes of dCN after upfront sunitinib relative to sunitinib alone. Methods: Patients with newly diagnosed mRCC receiving upfront sunitinib were identified from the International mRCC Database Consortium (IMDC) from 2006-2018. All CNs done after initial sunitinib were included, excluding CNs performed after sunitinib failure. The outcomes were overall survival (OS) and time to treatment failure (TTF). Kaplan Meier and multivariable Cox regression analyses were performed; dCN was analyzed as a time-varying covariate to account for immortal time bias. Results: The cohort included 708 patients of whom 53 (7.5%) underwent dCN at a median of 6.5 months (IQR 3.5,10.5) from diagnosis. Patients in the dCN group were more likely to have better Karnofsky performance status (KPS), intermediate IMDC risk, fewer metastatic sites, and response to upfront sunitinib (Table). There were 604 deaths during a median follow-up of 63 months. Median OS and TTF with dCN were 43.5 and 19.8 months vs. 9.4 and 4.3 months without, respectively. Upon multivariable analysis, dCN remained significantly associated with OS (HR 0.45, 95%CI 0.31-0.65; p < 0.001) but not TTF (HR 0.73, 95%CI 0.52-1.01; p = 0.056). Conclusions: Patients who received dCN were carefully selected and achieved long OS. With these benchmark outcomes, optimal selection criteria need to be identified and confirmation of the role of dCN in a clinical trial is warranted.
Variable | dCN | No CN | p-value |
---|---|---|---|
Age in years, median (IQR) | 61 (53-67) | 63 (55-70) | 0.08 |
KPS < 80, n (%) | 9 (15) | 256 (38) | < 0.001 |
Poor IMDC risk (vs intermediate), n (%) | 15 (25) | 333 (50) | < 0.001 |
> 1 Metastatic site, n (%) | 29 (55) | 518 (79) | < 0.001 |
Best response, n (%) | |||
Stable disease | 16 (26) | 225 (33) | < 0.001 |
Partial/complete response | 28 (46) | 110 (16) | |
Progressive disease | 12 (20) | 218 (32) | |
Unknown | 5 (8) | 119 (18) |
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