Evidence map›Paper›PMID 38687479›Full record

ArticleJAMA network open2024

Area Vulnerability and Disparities in Therapy for Patients With Metastatic Renal Cell Carcinoma.

Syed N Rahman, Jessica B Long, Sarah J Westvold, Michael S Leapman, Lisa P Spees, Michael E Hurwitz, Hannah D McManus, Cary P Gross, Stephanie B Wheeler, Michaela A Dinan

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Syed N RahmanDepartment of Urology, Yale School of Medicine, New Haven, Connecticut.
Jessica B LongYale Cancer Outcomes, Public Policy, and Effectiveness Research Center, Yale University, New Haven, Connecticut.
Sarah J WestvoldYale Cancer Outcomes, Public Policy, and Effectiveness Research Center, Yale University, New Haven, Connecticut.
Michael S LeapmanDepartment of Urology, Yale School of Medicine, New Haven, Connecticut.
Lisa P SpeesDepartment of Health Policy and Management, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill.
Michael E HurwitzDepartment of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Hannah D McManusDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina.
Cary P GrossYale Cancer Outcomes, Public Policy, and Effectiveness Research Center, Yale University, New Haven, Connecticut.
Stephanie B WheelerDepartment of Health Policy and Management, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill.
Michaela A DinanYale Cancer Outcomes, Public Policy, and Effectiveness Research Center, Yale University, New Haven, Connecticut.
Yale Cancer Center · USUniversity of North Carolina at Chapel Hill · USYale University · USDuke University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Investigation of the bidirectional relationship between kidney cancer treatment and dementiaR01CA226842 · NCI · YALE UNIVERSITY · PI DINAN, MICHAELA ANN · 2019 to 2023
$2.2M
Weight management and Black American women: Targeting social networks as a strategy to improve outcomesR01CA296842 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Marian L. Fitzgibbon, Yamile Molina · 2025 to 2026
$1.3M
NCATS NIH HHS UL1 TR001863NCI NIH HHS R01 CA226842NCI NIH HHS R01 CA296842
6 · The paper itself

Abstract

Importance: Area-level measures of sociodemographic disadvantage may be associated with racial and ethnic disparities with respect to receipt of treatment for metastatic renal cell carcinoma (mRCC) but have not been investigated previously, to our knowledge. Objective: To assess the association between area-level measures of social vulnerability and racial and ethnic disparities in the treatment of US Medicare beneficiaries with mRCC from 2015 through 2019. Design, Setting, and Participants: This retrospective cohort study included Medicare beneficiaries older than 65 years who were diagnosed with mRCC from January 2015 through December 2019 and were enrolled in fee-for-service Medicare Parts A, B, and D from 1 year before through 1 year after presumed diagnosis or until death. Data were analyzed from November 22, 2022, through January 26, 2024. Exposures: Five different county-level measures of disadvantage and 4 zip code-level measures of vulnerability or deprivation and segregation were used to dichotomize whether an individual resided in the most vulnerable quartile according to each metric. Patient-level factors included age, race and ethnicity, sex, diagnosis year, comorbidities, frailty, Medicare and Medicaid dual enrollment eligibility, and Medicare Part D low-income subsidy (LIS). Main Outcomes and Measures: The main outcomes were receipt and type of systemic therapy (oral anticancer agent or immunotherapy from 2 months before to 1 year after diagnosis of mRCC) as a function of patient and area-level characteristics. Multivariable regression analyses were used to adjust for patient factors, and odds ratios (ORs) from logistic regression and relative risk ratios (RRRs) from multinomial logistic regression are reported. Results: The sample included 15 407 patients (mean [SD] age, 75.6 [6.8] years), of whom 9360 (60.8%) were men; 6931 (45.0%), older than 75 years; 93 (0.6%), American Indian or Alaska Native; 257 (1.7%), Asian or Pacific Islander; 757 (4.9%), Hispanic; 1017 (6.6%), non-Hispanic Black; 12 966 (84.2%), non-Hispanic White; 121 (0.8%), other; and 196 (1.3%), unknown. Overall, 8317 patients (54.0%) received some type of systemic therapy. After adjusting for individual factors, no county or zip code-level measures of social vulnerability, deprivation, or segregation were associated with disparities in treatment. In contrast, patient-level factors, including female sex (OR, 0.78; 95% CI, 0.73-0.84) and LIS (OR, 0.48; 95% CI, 0.36-0.65), were associated with lack of treatment, with particularly limited access to immunotherapy for patients with LIS (RRR, 0.25; 95% CI, 0.14-0.43). Associations between individual-level factors and treatment in multivariable analysis were not mediated by the addition of area-level metrics. Disparities by race and ethnicity were consistently and only observed within the most vulnerable areas, as indicated by the top quartile of each vulnerability deprivation index. Conclusions and Relevance: In this cohort study of older Medicare patients diagnosed with mRCC, individual-level demographics, including race and ethnicity, sex, and income, were associated with receipt of systemic therapy, whereas area-level measures were not. However, individual-level racial and ethnic disparities were largely limited to socially vulnerable areas, suggesting that efforts to improve racial and ethnic disparities may be most effective when targeted to socially vulnerable areas.

Indexed as

Carcinoma, Renal CellHealthcare DisparitiesKidney NeoplasmsMedicareAgedAged, 80 and overFemaleHumansMaleRetrospective StudiesSocial VulnerabilitySocioeconomic FactorsUnited StatesVulnerable Populations

Identifiers

PMID38687479
PMCPMC11061765
OpenAlexW4396509845

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.