Evidence map›Paper›PMID 37584231›Full record

ArticleCancer medicine2023

Simple yet (more?) effective. Venous thromboembolism risk assessment model for germ cell tumour patients receiving first-line chemotherapy.

Wojciech Michalski, Grażyna Poniatowska, Joanna Jońska-Gmyrek, Agnieszka Żółciak-Siwińska, Inga Zastawna, Artur Lemiński, Anna Macios, Michał Jakubczyk, Tomasz Demkow, Paweł Wiechno

Abstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

10 authors.

Wojciech MichalskiDepartment of Urological Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0001-7746-0839
Grażyna PoniatowskaDepartment of Urological Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Joanna Jońska-GmyrekDepartment of Gynaecological Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Agnieszka Żółciak-SiwińskaDepartment of Gynaecological Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Inga ZastawnaClinical Centre of Cardiology and Rare Diseases of the Cardiovascular System, National Institute of Medicine of the Ministry of the Interior and Administration, Warsaw, Poland.
Artur LemińskiDepartment of Urology and Urological Oncology, Pomeranian Medical University, Szczecin, Poland.
Anna MaciosDepartment of Cancer Prevention, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0002-4279-5441
Michał JakubczykSGH Warsaw School of Economics, Institute of Econometrics, Collegium of Economic Analysis, Warsaw, Poland.
Tomasz DemkowDepartment of Urological Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paweł WiechnoDepartment of Urological Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGerm cell tumours (GCT) are highly curable malignancies. Venous thromboembolism (VTE) is a serious complication, needing better risk assessment models (RAM).

aimIdentification of VTE incidence and risk factors in metastatic GCT patients starting first-line chemotherapy. Developing a RAM and comparing it to Khorana risk score (KRS) and Padua Prediction Score (PPS). MATERIAL AND

methodsWe retrospectively analysed GCT patients staged IS-IIIC. VTE risk factors were identified with logistic regression. Area under curve of receiver operating characteristic (AUC-ROC), Akaike and Bayesian Information Criteria (AIC, BIC) were calculated for the developed RAM, KRS and PPS.

resultsAmong 495 eligible patients, VTE occurred in 69 (13.9%), including 40 prior to chemotherapy. Vein compression (OR: 8.96; 95% CI: 2.85-28.13; p < 0.001), clinical stage IIIB-IIIC (OR: 5.68; 95% CI: 1.82-17.70; p = 0.003) and haemoglobin concentration (OR for 1 g/dL decrease: 1.32; 95% CI: 1.03-1.67; p = 0.026) were significant in our RAM. KRS ≥ 3 (OR: 3.31; 95% CI: 1.77-6.20; p < 0.001), PPS 4-5 (OR: 3.06; 95% CI: 1.49-6.29; p = 0.002) and PPS > 5 (OR 8.05; 95% CI 3.79-17.13; p < 0.001) correlated with VTE risk. Diagnostic criteria (AUC-ROC, AIC, BIC) for the developed RAM, KRS and PPS were (0.885; 0.567; -1641), (0.588; 0.839; -1576) and (0.700; 0.799; -1585), respectively. In the numerical score, the optimal cut-off point for high-risk was ≥9, with sensitivity, specificity, positive and negative predictive value of 0.78, 0.77, 0.35 and 0.96, respectively.

conclusionsOur RAM, based on vein compression, clinical stage and haemoglobin concentration proved superior to both KRS and PPS. VTE is frequent in GCT patients.

Indexed as

Neoplasms, Germ Cell and EmbryonalVenous ThromboembolismAdolescentAdultFemaleHumansIncidenceMaleMiddle AgedNeoplasm StagingRetrospective StudiesRisk AssessmentRisk FactorsROC CurveYoung Adultdeep vein thrombosisgerm cell cancerpulmonary embolismrisk factors

Identifiers

PMID37584231
PMCPMC10557845

What Socratic 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 Socratic graph.