Evidence map›Paper›PMID 38798534›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Atopy improves survival and decreases risk of brain metastasis in cutaneous melanoma.

Corey Neff, Mackenzie Price, Gino Cioffi, Zhen Liu, Rabina Walsh, Jill S Barnholtz-Sloan, Kyle M Walsh, April K S Salama, Carey K Anders, Peter E Fecci and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Corey NeffDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-9479-2747
Mackenzie PriceDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-6369-0609
Gino CioffiTrans Divisional Research Program (TDRP) Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-3296-8652
Zhen LiuDepartment of Biostatistics, Duke University School of Medicine, Durham, NC, USA.
Rabina WalshDepartment of Dermatology, Duke University School of Medicine, Durham, NC, USA.
Jill S Barnholtz-SloanDepartment of Biostatistics, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-6190-9304
Kyle M WalshDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-5879-9981
April K S SalamaDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-8105-5374
Carey K AndersDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-9165-4074
Peter E FecciDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-2912-8695
Quinn T OstromDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0003-3469-7558

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI Laura Fish · 1985 to 2026
$174.8M
NCI NIH HHS P30 CA014236
6 · The paper itself

Abstract

Importance: Development of new therapies in melanoma has increased survival, and as a result more patients are living to develop brain metastasis (BrM). Identifying patients at increased risk of BrM is therefore of significant public health importance. Objective: To determine whether history of atopy is associated with improved survival or reduced incidence of BrM in cutaneous melanoma. Design: A retrospective cohort study conducted from June 2022 to March 2024. Setting: Population-based in states with Surveillance, Epidemiology and End Results (SEER) supported cancer registries. Participants: Individuals (≥65 years) diagnosed with cutaneous melanoma between January 1, 2008 and December 31, 2017 that are participants in traditional Medicare. Exposures: Individuals were compared that had history of atopy (allergic rhinitis, atopic dermatitis, asthma, and/or allergic/atopic conjunctivitis) diagnosed prior to melanoma diagnosis, ascertained using ICD-9 or ICD-10 codes in Medicare claims. Main Outcomes and Measures: Primary endpoints were diagnosis with a BrM or death during the follow-up period. Associations between atopy and endpoints were assessed using cox proportional hazards models to estimate hazard ratios (HR) and p-values. Results: A total of 29,956 cutaneous melanoma cases were identified (median age 76, 60% male and 97% non-Hispanic White). Overall, 7.1% developed BrM during follow up. Among the 35% that had history of atopy, the most common condition was atopic dermatitis (19%). After adjustment for demographic and prognostic factors, atopy was associated with a 16% decrease in death (HR=0.84 [95%CI:0.80-0.87], p Conclusions and Relevance: Atopy, particularly atopic dermatitis, was significantly associated with improved survival and decreased incidence of BrM. The improved survival associated with these conditions in the context of immunotherapy suggests that these conditions in the elderly may identify those with more robust immune function that may be more responsive to treatment.

Identifiers

PMID38798534
PMCPMC11118623

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.