Evidence map›Paper›PMID 37984720›Full record

ArticleJournal of the American Academy of Dermatology2024

Merkel cell carcinoma recurrence risk estimation is improved by integrating factors beyond cancer stage: A multivariable model and web-based calculator.

Aubriana M McEvoy, Daniel S Hippe, Kristina Lachance, Song Park, Kelsey Cahill, Mary Redman, Ted Gooley, Michael W Kattan, Paul Nghiem

Abstract read
In one paragraph

Article in Journal of the American Academy of Dermatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Merkel Cell Carcinoma.Hematology/oncology clinics of North America · 2024
    Review
  10. Article
  11. Review
  12. 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

9 authors.

Aubriana M McEvoyDepartment of Dermatology, University of Washington, Seattle, Washington; Division of Dermatology, Department of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Daniel S HippeClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Kristina LachanceDepartment of Dermatology, University of Washington, Seattle, Washington.
Song ParkDepartment of Dermatology, University of Washington, Seattle, Washington.
Kelsey CahillDepartment of Dermatology, University of Washington, Seattle, Washington.
Mary RedmanClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Ted GooleyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Michael W KattanDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.
Paul NghiemDepartment of Dermatology, University of Washington, Seattle, Washington; Fred Hutchinson Cancer Center, Seattle, Washington. Electronic address: pnghiem@uw.edu.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Understand & overcome resistance to PD-1P01CA225517 · NCI · UNIVERSITY OF WASHINGTON · PI PAUL NGHIEM · 2019 to 2026
$22.7M
NCI NIH HHS P01 CA225517NCI NIH HHS P30 CA015704
6 · The paper itself

Abstract

backgroundMerkel cell carcinoma (MCC) recurs in 40% of patients. In addition to stage, factors known to affect recurrence risk include: sex, immunosuppression, unknown primary status, age, site of primary tumor, and time since diagnosis. PURPOSE: Create a multivariable model and web-based calculator to predict MCC recurrence risk more accurately than stage alone.

methodsData from 618 patients in a prospective cohort were used in a competing risk regression model to estimate recurrence risk using stage and other factors.

resultsIn this multivariable model, the most impactful recurrence risk factors were: American Joint Committee on Cancer stage (P < .001), immunosuppression (hazard ratio 2.05; P < .001), male sex (1.59; P = .003) and unknown primary (0.65; P = .064). Compared to stage alone, the model improved prognostic accuracy (concordance index for 2-year risk, 0.66 vs 0.70; P < .001), and modified estimated recurrence risk by up to 4-fold (18% for low-risk stage IIIA vs 78% for high-risk IIIA over 5 years). LIMITATIONS: Lack of an external data set for model validation. CONCLUSION/RELEVANCE: As demonstrated by this multivariable model, accurate recurrence risk prediction requires integration of factors beyond stage. An online calculator based on this model (at merkelcell.org/recur) integrates time since diagnosis and provides new data for optimizing surveillance for MCC patients.

Indexed as

Carcinoma, Merkel CellNeoplasms, Unknown PrimarySkin NeoplasmsHumansInternetMaleNeoplasm Recurrence, LocalNeoplasm StagingPrognosisProspective StudiesRetrospective StudiesMerkel cell carcinomanomogramprognosisrecurrencerisk calculator

Identifiers

PMID37984720
PMCPMC10922724

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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.