Evidence map›Paper›PMID 36730884›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2023

A Clinical-Genetic Risk Score for Predicting Cancer-Associated Venous Thromboembolism: A Development and Validation Study Involving Two Independent Prospective Cohorts.

Andrés Muñoz, Cihan Ay, Ella Grilz, Sonia López, Carme Font, Vanesa Pachón, Victoria Castellón, Virginia Martínez-Marín, Mercedes Salgado, Eva Martínez and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
16.3field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. SEOM clinical guidelines on venous thromboembolism (VTE) and cancer (2023).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Guideline
  3. Venous and arterial thromboembolic events associated with osimertinib in patients with lung cancer: a study by the thrombosis and cancer group of the spanish society of medical oncology (SEOM).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  15. Time to move beyond risk assessment models for ambulatory cancer-associated thrombosis.Research and practice in thrombosis and haemostasis · 2025
    Article
  16. RResearch and practice in thrombosis and haemostasis · 2025
    Review
  17. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 9 institutions in 3 countries.

Andrés MuñozMedical Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.ORCID 0000-0001-6977-8249
Cihan AyClinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Ella GrilzClinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Sonia LópezGenomics of Complex Diseases Unit, Biomedical Research Institute Sant Pau (IIB-Sant Pau), Barcelona, Spain.
Carme FontCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.ORCID 0000-0002-3547-7373
Vanesa PachónCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.
Victoria CastellónCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.
Virginia Martínez-MarínCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.
Mercedes SalgadoCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.
Eva MartínezCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.
Julia CalzasCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.ORCID 0000-0002-9416-9514
Laura OrtegaMedical Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.ORCID 0000-0003-0456-7322
Ana RupérezCancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain.ORCID 0000-0003-2338-4257
Eduardo SalasScientific Department, Gendiag.exe, Barcelona, Spain.ORCID 0000-0002-6837-2471
Ingrid PabingerClinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Jose Manuel SoriaGenomics of Complex Diseases Unit, Biomedical Research Institute Sant Pau (IIB-Sant Pau), Barcelona, Spain.ORCID 0000-0002-6226-4293
Spanish Society of Hematology and Hemotherapy · ESHospital de Sant Pau · ESHospital General Universitario Gregorio Marañón · ESMedical University of Vienna · ATHospital Clínic de Barcelona · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario La Paz · ESMarqués de Valdecilla University Hospital · ESSechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeVenous thromboembolism (VTE) is a leading cause of death among patients with cancer. The Khorana score was developed for assessing the risk of VTE in outpatients with cancer receiving chemotherapy, but its accuracy in identifying patients at high risk has been questioned. The aim of this study was to develop and validate a clinical-genetic score that improves the assessment of VTE risk in oncology outpatients within 6 months of diagnosis.

methodsThe new score was developed using the data of 364 outpatients belonging to the Spanish ONCOTHROMB 12-01 population. In this cohort, clinical data associated with the risk of VTE were collected at the time of diagnosis, including the Khorana score. These patients were also genotyped for the 51 genetic variants known to be associated with VTE. Multivariate logistic regression was performed to determine the weight of each genetic and clinical variable in relation to VTE risk, allowing a clinical-genetic risk score (the ONCOTHROMB score) to be developed. The Khorana and the ONCOTHROMB scores were then compared via the area under the receiver operating characteristic curve (AUC), calibration, and the number of patients needed to treat. The new score was then validated in a study of 263 patients in the Vienna Cancer and Thrombosis Study population.

resultsNine genetic variants, tumor site, TNM stage, and a body mass index of > 25 kg/m

conclusionThe ONCOTHROMB score for VTE risk in outpatients with cancer, which takes into account both clinical and genetic variables, better identifies patients who might benefit from primary thromboprophylaxis than does the Khorana score.

Indexed as

NeoplasmsThrombosisVenous ThromboembolismAnticoagulantsHumansProspective StudiesRisk AssessmentRisk FactorsAnticoagulants

Identifiers

PMID36730884
PMCPMC10414737
OpenAlexW4318954454

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.