Evidence map›Paper›PMID 41249955›Full record

ArticleBMC cancer2025

Tinzaparin for the prevention of thromboembolic events in ambulatory patients with metastatic colorectal cancer receiving first line treatment: a randomised, clinical trial design.

Mercedes Salgado, Juan de la Camara-Gómez, Ignacio García-Escobar, Renata-Carola Álvarez-Llosa, Paula González-Villarroel, David Fernández Garay, Montse Pàmpols-Felip, Mónica Guillot-Morales, Francisco José Pelegrín-Mateo, Encarnación Jimenez-Orozco and 21 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05625932 (Prophylaxis of Venous Thromboembolic Disease With Low Molecular Weight), which is not on this 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.

NCT05625932 phase3completednot on this map

Prophylaxis of Venous Thromboembolic Disease With Low Molecular Weight (LMWH) (TINzaparin) in Patients With Metastatic Colorectal Cancer Who Start the First Line of Treatment.

TypeinterventionalSponsorGalician Research Group on Digestive TumorsRan2023 to 2025Enrolled232ConditionsColorectal Cancer Metastatic, ThromboembolismArmsTinzaparin
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

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

31 authors.

Mercedes SalgadoMedical Oncology Department, Complexo Hospitalario de Ourense, Ourense, Spain.ORCID http://orcid.org/0000-0003-4134-1509
Juan de la Camara-GómezMedical Oncology Department, Complexo Hospitalario Universitario, A Coruña, Spain.ORCID http://orcid.org/0009-0001-3534-7923
Ignacio García-EscobarMedical Oncology Department, Hospital General Universitario de Toledo, Toledo, Spain.ORCID http://orcid.org/0000-0002-1068-0455
Renata-Carola Álvarez-LlosaMedical Oncology Department, Complexo Hospitalario de Ourense, Ourense, Spain.ORCID http://orcid.org/0009-0006-2669-222X
Paula González-VillarroelAlvaro Cunqueiro Hospital, Vigo, Spain.ORCID http://orcid.org/0000-0002-4930-6823
David Fernández GarayHospital Costa del Sol, Marbella, Spain.ORCID http://orcid.org/0009-0006-4789-5384
Montse Pàmpols-FelipMedical Oncology Department, Hospital Arnau de Vilanova, Lleida, Spain.ORCID http://orcid.org/0009-0006-4870-9440
Mónica Guillot-MoralesMedical Oncology Department, Hospital Universitario Son Espases, Palma de Mallorca, Spain.ORCID http://orcid.org/0000-0001-7509-146X
Francisco José Pelegrín-MateoHospital General Universitario Dr. Balmis, Alicante, Spain.ORCID http://orcid.org/0000-0002-4340-9493
Encarnación Jimenez-OrozcoHospital Universitario Jerez de la Frontera, Cádiz, Spain.ORCID http://orcid.org/0000-0002-3392-9321
Javier SastreHospital Clinico San Carlos, Madrid, Spain.ORCID http://orcid.org/0000-0001-6538-0065
Eva Martínez de CastroMedical Oncology Department, University Hospital Marqués de Valdecilla, IDIVAL, Santander, Spain.ORCID http://orcid.org/0000-0002-5772-0741
Eva ComaInstitut Català d'Oncologia L'Hospitalet, Hospitalet De Llobregat , Barcelona, Spain.ORCID http://orcid.org/0009-0008-7312-8458
Lorena París BouzasCentro Oncológico de Galicia, A Coruña, Spain.ORCID http://orcid.org/0009-0007-7579-0691
Ana Isabel Ferrer-PérezHospital Obispo Polanco, Teruel, Spain.ORCID http://orcid.org/0000-0003-0464-5976
Elisabet Mompradé-OlivéInstitut Catala D'Oncologia - Hospital Universitari Germans Trias i Pujol, Badalona, Spain.ORCID http://orcid.org/0000-0002-5807-7946
Antia Cousillas-CastiñeirasComplexo Hospitalario de Pontevedra, Pontevedra, Spain.ORCID http://orcid.org/0000-0001-5586-1818
Marta Covela-RúaHospital Universitario Lucus Augusti (HULA), Lugo, Spain.ORCID http://orcid.org/0000-0003-3360-3070
Mariam RojasHospital Clínic de Barcelona, Barcelona, Spain.ORCID http://orcid.org/0009-0001-7837-020X
Rosa QuerolMedical Oncology Service, Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona Sabadell, Barcelona, Spain.ORCID http://orcid.org/0009-0008-5174-4081
Luis Robles DíazMedical Oncology Department, Hospital Universitario 12 de Octubre, Instituto de Investigación i+12, Madrid, Spain.ORCID http://orcid.org/0000-0002-8909-8520
Marta MerinoMedical Affairs Department, LEO Pharma, Barcelona, Spain.ORCID http://orcid.org/0009-0003-5139-162X
Mireia GilMedical Oncology Department, General University Hospital, Valencia, Spain.ORCID http://orcid.org/0000-0002-4508-7395
Manuel Sánchez-CánovasHospital General Universitario Morales Meseguer, Murcia, Spain.ORCID http://orcid.org/0000-0001-8687-4101
Teresa ElíasInstituto de Biomedicina (IBIS), Hospital Universitario Virgen del Rocío, Sevilla, Spain.ORCID http://orcid.org/0000-0002-6181-3617
David Marrupe-GonzálezHospital Universitario de Móstoles, Madrid, Spain.ORCID http://orcid.org/0000-0002-7986-2783
Belén Sánchez-GilHospital General La Mancha Centro, Ciudad Real, Spain.
Marta Carmona-CamposHospital Clínico Universitario de Santiago CHUS, Coruña, Spain.ORCID http://orcid.org/0009-0003-6890-038X
María García-FerrónHospital Infanta Cristina de Parla, Madrid, Spain.
José Manuel SoriaGenomics of Complex Diseases Unit, Biomedical Research Institute Sant Pau (IIB-Sant Pau) Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0002-6226-4293
Andrés MuñozMedical Oncology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain. andresmunmar@hotmail.com.ORCID http://orcid.org/0000-0001-6977-8249

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is the third most commonly diagnosed cancer worldwide. CRC leads to increased activation of the clotting system. Since CRC patients present a higher rate of bleeding, careful evaluation of the risk/benefits of anticoagulant prophylaxis is necessary.

aimsTo evaluate low molecular weight heparin (LMWH) for primary thromboprophylaxis in metastatic CRC outpatients receiving first-line systemic cancer therapy.

methodsPROTINCOL (NCT05625932) is a randomized, open-label (PROBE), multicenter study. Patients will receive tinzaparin (75 IU/kg) or no pharmacological prophylaxis for 4 months and will be stratified based on: BRAF/RAS mutation, primary resection tumor and antiangiogenic therapy. The study outcomes will be assessed by a blinded central independent adjudication committee. The primary efficacy endpoints will include the cumulative incidence of any venous thromboembolism (VTE) event (symptomatic or incidental) including symptomatic central venous catheter VTE. Secondary variables will be clinically relevant bleedings, health-related quality of life and the predictive value of validated risk assessment scales of VTE, including the genetic risk score (TIC-ONCO). Our hypothesis is that prophylactic LMWH will reduce the 55% relative risk to an estimated VTE incidence of 13.5%. A total of 526 patients will be required. DISCUSSION: Risk prediction of chemotherapy-associated VTE is a compelling challenge in oncology, as VTE may result in treatment delays, impaired quality of life, and increased mortality. Patients with a single type of metastatic cancer with a high risk of VTE will be selected for study inclusion. For the first time in ambulatory prophylaxis of cancer-associated thrombosis, a precision medicine approach will be used in a clinical trial. If the individualization of antithrombotic prophylaxis can reduce the complications of outpatient cancer treatment and be cost effective, it would be of great value in the future care of patients with metastatic CRC.

trial registrationNCT05625932. Registered on 15 Nov 2022. TRIAL STATUS: The trial started recruitment on March 2023.

Indexed as

Colorectal NeoplasmsFibrinolytic AgentsHeparin, Low-Molecular-WeightTinzaparinVenous ThromboembolismAdultAgedAnticoagulantsFemaleHumansMaleMiddle AgedMulticenter Studies as TopicNeoplasm MetastasisQuality of LifeRandomized Controlled Trials as TopicAnticoagulantsFibrinolytic AgentsHeparin, Low-Molecular-WeightTinzaparinColorectal cancerGeneticsMetastaticRisk factorsThromboprophylaxisVenous thromboembolism

Identifiers

PMID41249955
PMCPMC12621363

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Registered trials

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.