ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1327

Association of Rheumatoid Arthritis and Frailty Status with Mortality in Patients with Renal Cell Carcinoma

Sherwin Novin1, Sarah Holt2, Maya Swaminathan3, Jonathan Wright2, John Gore2, Kimme Hyrich4, Sizheng Zhao5, Jeffrey Sparks6, Una Makris7, Maria Suarez-Almazor8, Petros Grivas2, Sarah Psutka2 and Namrata Singh9, 1University of Washington, Seattle, WA, 2University of Washington, Seattle, 3MultiCare, Newcastle, WA, 4Centre for Musculoskeletal Research, The University of Manchester, Manchester, United Kingdom, 5Centre for Musculoskeletal Research, The University of Manchester, Liverpool, United Kingdom, 6Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA, Boston, MA, 7UT Southwestern Medical Center and Dallas VA, Dallas, TX, 8MD Anderson Cancer Center, Houston, TX, 9University of Washington, Bellevue, WA

Meeting: ACR Convergence 2024

Keywords: Aging, Mortality, Oncology, rheumatoid arthritis

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 17, 2024

Title: RA – Diagnosis, Manifestations, & Outcomes Poster II

Session Type: Poster Session B

Session Time: 10:30AM-12:30PM

Background/Purpose: Few studies have evaluated clinical outcomes and prognosis of patients with cancer with and without rheumatoid arthritis (RA). Renal cell carcinoma (RCC) is particularly understudied in relation to RA, but evaluation is highly relevant due to standard use of immune checkpoint inhibitors in management. With potential conflicts in the treatment of both RA and RCC, there exists a need to further elucidate outcomes in this unique patient population. Given the adverse outcomes associated with frailty, often present in both conditions, we sought to evaluate all-cause and cancer-specific mortality with a focus on the interactions between frailty, RCC, and RA.

Methods: We collected patient data via the linked Surveillance Epidemiology and End Results cancer registry and Medicare (SEER-Medicare) database. We included non-metastatic patients with the most common subtype of RCC, clear cell Renal Cell Carcinoma (ccRCC), diagnosed from 2004-2017 using ICD-9 and ICD-10 codes. Patients with pre-existing RA were identified if they had ≥2 ICD-9/10 codes for RA within 2 years prior to diagnosis, separately coded 30-365 days apart. Validated Claims-based Frailty (Kim et al 2018) and National Cancer Institute (NCI) Comorbidity indices were extracted within 365 days prior to ccRCC diagnosis. Cox proportional hazards regression models evaluated the association between RA and both all-cause and cancer-specific mortality, adjusting for demographics, socioeconomic status, comorbidities, and cancer stage. For cancer-specific mortality, competing risk analyses were performed and sub-distribution hazard ratios (HR) with 95% confidence intervals (CI) were calculated. Effect modification by frailty status in association with RA and mortality outcomes was assessed.

Results: We identified 31,989 patients with non-metastatic ccRCC, of whom 802 (2.5%) had pre-existing RA (Table 1); most had Stage I-II disease (80.7%). Overall, 12.3% met criteria for frailty, including 20.5% of patients with RA vs. 12.0% of patients without RA (p< 0.001).

We observed interaction between RA and frailty on all-cause mortality (p = 0.01). The presence of RA in non-frail patients was associated with a significant increased risk of all-cause mortality compared to those without RA (HR 1.15 [95% CI 1.03 – 1.28]). Frail patients with RA (HR 0.91 [95% CI 0.76 – 1.10]), however, did not have a significant difference in all-cause mortality compared to those without RA. No interaction was observed between RA and frailty for cancer-specific mortality (Table 2).

The presence of frailty independently was associated with a significantly increased risk of cancer-specific mortality (HR 1.48 [95% CI 1.36 – 1.61]) while RA was not (HR 1.05 [95% CI 0.88 – 1.25]).

Conclusion: RA was an independent risk factor for all-cause mortality in non-frail patients with non-metastatic ccRCC but not for mortality in frail patients. The presence of frailty, but not RA, was an independent risk factor for cancer specific mortality. Limitations include retrospective nature, selection bias, unmeasured confounders. Our findings are hypothesis-generating and can be used to guide point-of-care discussions in clinic and underscore the importance of further characterizing frailty status.

Supporting image 1

Table 1. Baseline Characteristics of the Cohort Stratified by Rheumatoid Arthritis (RA) Status

Supporting image 2

Table 2. Adjusted Hazard Ratios in Patients with RA vs without RA


Disclosures: S. Novin: None; S. Holt: None; M. Swaminathan: None; J. Wright: None; J. Gore: None; K. Hyrich: None; S. Zhao: None; J. Sparks: Boehringer-Ingelheim, 2, 5, Bristol-Myers Squibb(BMS), 2, 5, Gilead, 2, Janssen, 2, Pfizer, 2, UCB, 2; U. Makris: None; M. Suarez-Almazor: Syneos Health, 1; P. Grivas: None; S. Psutka: None; N. Singh: None.

To cite this abstract in AMA style:

Novin S, Holt S, Swaminathan M, Wright J, Gore J, Hyrich K, Zhao S, Sparks J, Makris U, Suarez-Almazor M, Grivas P, Psutka S, Singh N. Association of Rheumatoid Arthritis and Frailty Status with Mortality in Patients with Renal Cell Carcinoma [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/association-of-rheumatoid-arthritis-and-frailty-status-with-mortality-in-patients-with-renal-cell-carcinoma/. Accessed .
  • Tweet
  • Email
  • Print

« Back to ACR Convergence 2024

ACR Meeting Abstracts - https://acrabstracts.org/abstract/association-of-rheumatoid-arthritis-and-frailty-status-with-mortality-in-patients-with-renal-cell-carcinoma/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology