Evidence map›Paper›PMID 38766175›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Toward personalized skin cancer care: multiple skin cancer development in five cohorts.

Lee Wheless, Kai-Ping Liao, Siwei Zheng, Yao Li, Lydia Yao, Yaomin Xu, Christopher Madden, Jacqueline Ike, Isabelle T Smith, Dominique Mosley and 5 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

15 authors.

Lee WhelessTennessee Valley Healthcare System VA Medical Center.ORCID 0000-0002-8162-5971
Kai-Ping LiaoUniversity of Texas MD Anderson Cancer Center, Department of Health Services Research.
Siwei ZhengDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Yao LiUniversity of Texas MD Anderson Cancer Center, Department of Health Services Research.
Lydia YaoDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Yaomin XuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0002-3752-4006
Christopher MaddenState University of New York Downstate College of Medicine, Brooklyn, New York.
Jacqueline IkeMeharry Medical College, Nashville, Tennessee.
Isabelle T SmithVanderbilt University, Nashville, Tennessee.
Dominique MosleyVanderbilt University School of Medicine, Nashville, Tennessee.
Sarah GrossarthQuillen College of Medicine, East Tennessee State University, Johnson City, TN.
Rebecca I HartmanVA Boston Healthcare System.
Otis WilsonTennessee Valley Healthcare System VA Medical Center.
Adriana HungTennessee Valley Healthcare System VA Medical Center.
Mackenzie R WehnerUniversity of Texas MD Anderson Cancer Center, Department of Health Services Research.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Skin Cancer Risks and Risk Prediction in Patients with Actinic KeratosisK08CA263298 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Mackenzie Rachel Wehner · 2022 to 2026
$1.3M
Identifying clinical and genetic factors for risk of multiple skin cancers in organ transplant recipientsIK2CX002452 · VA · VETERANS HEALTH ADMINISTRATION · PI LEE E WHELESS · 2023 to 2026
–
Risk Factors for Clinically Aggressive Melanoma in VeteransIK2CX002531 · VA · VA BOSTON HEALTH CARE SYSTEM · PI Rebecca Ivy Hartman · 2024 to 2026
–
CSRD VA IK2 CX002452CSRD VA IK2 CX002531NCATS NIH HHS UL1 TR000445NCI NIH HHS K08 CA263298NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Importance: Many patients will develop more than one skin cancer, however most research to date has examined only case status. Objective: Describe the frequency and timing of the treatment of multiple skin cancers in individual patients over time. Design: Longitudinal claims and electronic health record-based cohort study. Setting: Vanderbilt University Medical Center database called the Synthetic Derivative, VA, Medicare, Optum Clinformatics Participants: All patients with a Current Procedural Terminology code for the surgical management of a skin cancer in each of five cohorts. Exposures: None. Main Outcomes and Measures: The number of CPT codes for skin cancer treatment in each individual occurring on the same day as an ICD code for skin cancer over time. Results: Our cohort included 5,508,374 patients and 13,102,123 total skin cancers treated. Conclusions and Relevance: Nearly half of patients treated for skin cancer were treated for more than one skin cancer. Patients who have not developed a second skin cancer by 2 years after the first are unlikely to develop multiple skin cancers within the following 5 years. Better data formatting will allow for improved granularity in identifying individuals at high risk for multiple skin cancers and those unlikely to benefit from continued annual surveillance. Resource planning should take into account not just the number of skin cancer cases, but the individual burden of disease.

Indexed as

cohort studyepidemiologyskin cancer

Identifiers

PMID38766175
PMCPMC11100848

What OpenQuestion holds

Textmetadata
LicenceCC0
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.