Abstract 1900P
Background
The effectiveness of CN is still uncertain despite two significant trials, SURTIME and CARMENA, which aimed to demonstrate its benefits for mccRCC. These trials, conducted with Sunitinib as the standard treatment, did not provide evidence supporting the use of CN.
Methods
We identified stage IV mccRCC only patients (pts) who received IO with or without surgery in the NCDB 2004-2020. Overall survival (OS) was calculated among three groups of IO alone (group (gr)1), IO followed by CN (gr2), CN followed by IO (gr3). Cox models compared OS by treatment group after adjusting for sociodemographic, health, and facility variables.
Results
From 1,549,101 renal cancer cases, 7,367 met our criteria. 2.8% of ccRCC had sarcomatoid histology. Pts in the gr 2 and gr 3 had 63%, 95% CI [0.304 - 0.460] and 47%, 95% CI [0.492-0.571] (P= 0.001) risk reduction in mortality compared to gr 1.Black race compared to white race, Medicare pts compared to privately insured, and pts treated at a comprehensive community cancer center compared to academic center had an increased mortality risk by 15%, 95% CI [1.025-1.290] (P= 0.017), 12%, 95% CI [1.017-1.242] (P= 0.021), 17%, 95% CI [1.092-1.260] (P= 0.001) respectively. Median income quartiles ranging > 63k, had 22% reduction in mortality over income quartiles < 40k, 95% CI [0.696-0.888] (P= 0.044). Regardless of the sequence of CN, partial nephrectomy was minimally used. Pts in gr 3 had a 40% increased mortality risk compared to pts in gr 3, 95% CI [1.126-1.735] (P= 0.002).
Conclusions
Pts receiving CN regardless of sequence with IO did better than IO alone in this national registry-based adjusted analysis for mccRCC. Over the past few decades, the understanding of the role of CN has undergone changes, and while we await additional trial outcomes, the current evidence supports the notion that select mRCC patients can benefit from CN.
Table: 1900P
IO (%) 95% CI | IO⋄CN (%) 95% CI | CN⋄IO (%) 95% CI | |
2 YRS FOLLOW UP | 35.82 [34.44-37.20] | 73.87 [68.48-78.49] | 58.78 [56.75-60.74] |
5 YRS FOLLOW UP | 13.01 [11.32-14.82] | 43.17 [33.94-52.05] | 34 [31.32-36.39] |
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1706P - Time to full approval of novel anticancer medicines granted accelerated approval and implications for reform of the accelerated approval pathway
Presenter: Thomas Hwang
Session: Poster session 23
1707P - Cancer drug prices in the US: Efficacy, innovation, clinical trial evidence, and epidemiology
Presenter: Christoph Michaeli
Session: Poster session 23
1708P - The registration pathways in China for globally developed novel anticancer drugs
Presenter: Da-wei Wu
Session: Poster session 23
1709P - Influence of censoring on conclusions of FDA-approved cancer drugs using the modified time to treatment failure
Presenter: Jonathan Ofer
Session: Poster session 23
1710P - Protocol waivers and consequences on treatment safety and efficacy in the Drug Rediscovery Protocol (DRUP)
Presenter: Laurien Zeverijn
Session: Poster session 23
1711P - The DRUP-like clinical trials family: A distributed European trial network for equitable access to precision medicine
Presenter: Hans Gelderblom
Session: Poster session 23
1712P - Implementation of a molecular pre-screening program (MPP) in a network of public cancer centres for phase I clinical trial (Ph1-CT) candidates: The PREICO program
Presenter: Juan José Soto Castillo
Session: Poster session 23
1713P - Non-inferiority oncology clinical trials in major journals: Purposes, methods and results
Presenter: Rafael Barreto
Session: Poster session 23
1714P - Geographical disparities in access to cancer clinical trials in Korea
Presenter: Sokbom Kang
Session: Poster session 23
1715P - Analysis of the adequacy of control arms in oncology randomized clinical trials published between 2017 and 2021: A meta-research study
Presenter: Alessandro Rossi
Session: Poster session 23