Evidence map›Paper›PMID 31042264›Full record

ArticleJAMA dermatology2019

Risk Factors for Lymphatic and Hematogenous Dissemination in Patients With Stages I to II Cutaneous Melanoma.

Laura Calomarde-Rees, Rosario García-Calatayud, Celia Requena Caballero, Esperanza Manrique-Silva, Víctor Traves, Zaida García-Casado, Virtudes Soriano, Rajiv Kumar, Eduardo Nagore

Open access · bronzeAbstract read
In one paragraph

Article in JAMA dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  9. Metabolic insights into tumor lymph node metastasis in melanoma.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  10. Utility and Micro-Costing Framework forDiagnostics (Basel, Switzerland) · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Laura Calomarde-ReesDepartment of Dermatology, Instituto Valenciano de Oncología, València, Spain.
Rosario García-CalatayudSchool of Medicine, Universidad Católica de Valencia San Vicente Mártir, València, Spain.
Celia Requena CaballeroDepartment of Dermatology, Instituto Valenciano de Oncología, València, Spain.
Esperanza Manrique-SilvaDepartment of Dermatology, Instituto Valenciano de Oncología, València, Spain.
Víctor TravesDepartment of Pathology, Instituto Valenciano de Oncología, València, Spain.
Zaida García-CasadoLaboratory of Molecular Biology, Instituto Valenciano de Oncología, València, Spain.
Virtudes SorianoDepartment of Medical Oncology, Instituto Valenciano de Oncología, València, Spain.
Rajiv KumarDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Eduardo NagoreDepartment of Dermatology, Instituto Valenciano de Oncología, València, Spain.
Fundación Instituto Valenciano de Oncología · ESValencia Catholic University Saint Vincent Martyr · ESGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The lymphatic and the hematogenous pathways have been proposed for disease progression in cutaneous melanoma, but association with recurrence has not been studied separately to date. Objective: To identify the risk factors associated with lymphatic and hematogenous metastasis. Design, Setting, and Participants: This retrospective cohort study included 1177 patients with malignant melanoma treated at Instituto Valenciano de Oncología, València, Spain. Data were retrieved from the melanoma database from January 1, 2000, through December 31, 2015, and analyzed from June 1 to 30, 2018. Exposure: Malignant melanoma at stages I to II. Main Outcomes and Measures: Analyses of survival free of lymphatic and hematogenous metastasis were performed using Kaplan-Meier curves and Cox proportional hazards regression. Results: For the 1177 patients included in the study analysis (51.1% women; median age at diagnosis, 55 years [interquartile range, 42-68 years), median follow-up was 75 months (interquartile range, 33-121 months); 108 (9.2%) developed lymphatic metastasis, and 108 (9.2%) developed hematogenous metastasis. In the multivariate analysis, being older than 55 years (hazard ratio [HR], 1.9; 95% CI, 1.2-3.1), tumor in the head/neck (HR, 1.7; 95% CI, 1.0-2.9) and acral locations (HR, 2.4; 95% CI, 1.3-4.5), greater Breslow thickness (HR for >4.00 mm, 5.4; 95% CI, 2.4-12.4), and presence of vascular invasion (HR, 3.2; 95% CI, 0.9-10.6) were associated with lymphatic spreading. Hematogenous metastasis was associated with greater Breslow thickness (HR for >4.00 mm, 10.4; 95% CI, 3.6-29.7), the absence of regression (HR, 0.1; 95% CI, 0.0-1.0), TERT promoter mutations (HR, 2.9; 95% CI, 1.5-5.7), and BRAF mutations (HR, 1.9; 95% CI, 1.1-3.6). Conclusions and Relevance: Risk factors associated with lymphatic and hematogenous metastasis differ. Follow-up and adjuvant treatment strategies may therefore need to be adapted to individual clinical, histopathologic, and molecular characteristics.

Indexed as

AdultAgedAge FactorsCohort StudiesFemaleHumansLongitudinal StudiesLymphatic MetastasisMaleMelanomaMiddle AgedNeoplasm StagingRetrospective StudiesRisk FactorsSkin Neoplasms

Identifiers

PMID31042264
PMCPMC6495361
OpenAlexW2943211708

What OpenQuestion holds

Textmetadata
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.