Evidence map›Paper›PMID 37910523›Full record

Trial reportPloS one2023

Biosimilar versus branded enoxaparin to prevent postoperative venous thromboembolism after surgery for digestive tract cancer: Randomized trial.

Chadli Dziri, Wafa Ben Hmida, Wejih Dougaz, Mehdi Khalfallah, Imen Samaali, Hichem Jerraya, Ibtissem Bouasker, Ramzi Nouira

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02444572 (Comparison of Thromboembolic Events in Patients Undergoing Gastrointestinal Cancer Surgery and Thromboprophylactic Treatment With Two Enoxaparin Formulations), 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
0.6field-weighted citation impact, top 31% 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.

NCT02444572 phase4completednot on this map

Comparison of Thromboembolic Events in Patients Undergoing Gastrointestinal Cancer Surgery and Thromboprophylactic Treatment With Two Enoxaparin Formulations (ENOXA® vs Lovenox®)

TypeinterventionalSponsorLes Laboratoires des Médicaments StérilesRan2015 to 2020Enrolled168ConditionsGastrointestinal Neoplasms, Thromboembolic EventArmsEnoxaparin 4000 IU
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

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

8 authors at 2 institutions in 1 country.

Chadli DziriTunis Medical School, Tunis El Manar University, Tunis, Tunisia.ORCID 0000-0003-2779-0930
Wafa Ben HmidaDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Wejih DougazDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Mehdi KhalfallahDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Imen SamaaliDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Hichem JerrayaDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Ibtissem BouaskerDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Ramzi NouiraDepartment B of General Surgery, Charles Nicolle's Hospital, Tunis El Manar University, Tunis, Tunisia.
Hôpital Charles-Nicolle · TNTunis El Manar University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer and/or major surgery are two factors that predispose to post-operative thrombosis. The annual incidence of venous thromboembolic disease (VTED) in cancer patients was estimated at 0.5%-20%. Surgery increases the risk of VTED by 29% in the absence of thromboprophylaxis. Enoxaparin is a low molecular weight heparin that is safe and effective. Branded Enoxaparin and biosimilar Enoxaparin are two enoxaparin treatments. This study aimed to compare Branded Enoxaparin with biosimilar Enoxaparin in patients operated on for digestive cancer regarding the prevention of postoperative thrombosis event, to compare the tolerance of the two treatments and to identify independent predictive factors of thromboembolic incident. A randomized controlled trial conducted in a single-centre, surgical department B of Charles Nicolle Hospital, over a 5-year period from October 12th, 2015, to July 08th, 2020. We included all patients over 18 who had cancer of the digestive tract newly diagnosed, operable and whatever its nature, site, or stage, operated on in emergency or elective surgery. The primary endpoint was any asymptomatic thromboembolic event, demonstrated by systematic US Doppler of the lower limbs on postoperative day 7 to day 10. The sonographer was unaware of the prescribed treatment (Branded Enoxaparin [BE] or biosimilar Enoxaparin [BSE]). Of one hundred sixty-eight enrolled patients, six patients (4.1%) had subclinical venous thrombosis. Among those who had subclinical thrombosis, four patients (5.6%) were in the Branded Enoxaparin group and two patients (2.7%) in the Biosimilar Enoxaparin group without statistically significant difference (p = 0.435). Analysis of the difference in means using Student's t test demonstrated the equivalence of the two treatments. Our study allowed us to conclude that there was no statistically significant difference between Branded Enoxaparin and Biosimilar Enoxaparin regarding the occurrence of thromboembolic accidents postoperatively. BE and BSE are equivalent. Trial registration. Trial registration: The trial was registered on CLINICALTRIALS.GOV under the number NCT02444572.

Indexed as

Biosimilar PharmaceuticalsGastrointestinal NeoplasmsThrombosisVenous ThromboembolismVenous ThrombosisAnticoagulantsEnoxaparinHumansPostoperative ComplicationsAnticoagulantsBiosimilar PharmaceuticalsEnoxaparin

Identifiers

PMID37910523
PMCPMC10619849
OpenAlexW4388125860

What OpenQuestion holds

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LicenceCC BY
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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.