Evidence map›Paper›PMID 40894050›Full record

ArticleResearch square2025

Geospatial heterogeneity of hotspots for incidence and late-stage diagnosis of breast, colorectal, and lung cancer.

Andrew P Loehrer, Heather A Carlos, Julia E Weiss, Chelsea V Leversedge, Julia E Katter, Joseph D Phillips, Dana Ferrari-Light, Tracy Onega, Xun Shi

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In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

9 authors.

Andrew P LoehrerDartmouth-Hitchcock Medical Center.
Heather A CarlosGeisel School of Medicine at Dartmouth.
Julia E WeissGeisel School of Medicine at Dartmouth.
Chelsea V LeversedgeGeisel School of Medicine at Dartmouth.
Julia E KatterGeisel School of Medicine at Dartmouth.
Joseph D PhillipsDartmouth-Hitchcock Medical Center.
Dana Ferrari-LightDartmouth-Hitchcock Medical Center.
Tracy OnegaUniversity of Utah, Huntsman Cancer Institute.
Xun ShiDartmouth College.

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
Geospatial drivers of cancer care disparities and their susceptibility to health policy changesK08CA263546 · NCI · DARTMOUTH-HITCHCOCK CLINIC · PI Andrew Phillip Loehrer · 2022 to 2026
$869k
NCI NIH HHS K08 CA263546NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

Purpose: Cancer control relies on the identification of populations at risk (hotspots) of new or late-stage cancer diagnoses. However, the extent to which hotspots differ between cancer sites or between outcome measures has been poorly characterized. We sought to determine the geospatial heterogeneity of hotspots of breast, colorectal, and lung cancer incidence and late-stage diagnoses. Methods: We identified adult patients diagnosed with female breast, colorectal, and lung cancer between 2010 and 2019 in Indiana. To identify hotspots for incidence and late-stage diagnoses, we disaggregated the patient residential location information from the Census block group level to the approximated individual point level. Statistically significant hotspots were identified with kernel ratio estimation. Total areas of hotspots and overlap between hotspots were compared. Results: 117,305 patients diagnosed with breast (n=51,623), colorectal (n=25,160), and lung (n=37,522) cancer were included. Geospatial visualization demonstrated marked spatial deviation, with little overlapping area between incidence and late-stage hotspots for all three cancer sites (32km Conclusions: Our results demonstrate considerable geospatial heterogeneity of hotspots between different outcome measures and different sites of cancer. However, there are greater overlapping areas of late-stage hotspots, especially for breast and lung cancer. The use of disaggregated spatial data enables more granular, precise comparison of cancer hotspots. Greater overlap between late-stage breast and lung cancer suggests similar spatial drivers and the potential for coordinated cancer control interventions.

Indexed as

Access to CareCancer ControlCancer IncidenceHotspotPrevention

Identifiers

PMID40894050
PMCPMC12393488

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.