Evidence map›Paper›PMID 41381053›Full record

ArticleFundamental & clinical pharmacology2026

Linking the NETSARC+ National Sarcoma Database With the SNDS to Evaluate Adjuvant and/or Neoadjuvant Therapy: Report on the Linkage Process and Result (Health Data Hub's DEEPSARC Pilot Project).

Erwan Drezen, André Happe, Vincent Thevenet, Nicolas Penel, François Gouin, François Le Loarer, Gonzague Du Bouexic De Pinieux, Hugo Crochet, Claire Chemin Airiau, Françoise Ducimetiere and 3 more

Abstract read
In one paragraph

Article in Fundamental & clinical pharmacology, 2026. 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

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

13 authors.

Erwan DrezenCUBR SAS, Rennes, France.
André HappeUniversity of Rennes, Rennes, France.
Vincent ThevenetINSERM, Institut Bergonié, CIC 1401, Euclid/F-CRIN Clinical Trials Platform, University of Bordeaux, Bordeaux, France.
Nicolas PenelMedical Oncology Department, Oscar Lambret Cancer Center and Lille University, Lille, France.
François GouinCentre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
François Le LoarerInstitut Bergonié, University of Bordeaux, Bordeaux, France.
Gonzague Du Bouexic De PinieuxCHU Tours, University of Tours, Tours, France.
Hugo CrochetCentre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
Claire Chemin AiriauCentre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
Françoise DucimetiereCentre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
Simone Mathoulin PelissierINSERM, Institut Bergonié, CIC 1401, Bordeaux Population Health U1219 Epicene Team, University of Bordeaux, Bordeaux, France.
Jean-Yves BlayDepartment of Medicine, Léon Bérard Center, Lyon, France.
Emmanuel OgerUniversity of Rennes, Rennes, France.ORCID https://orcid.org/0000-0001-9837-2977

Funding

EURACAN 739521Health Data Hub
6 · The paper itself

Abstract

backgroundDEEPSARC, one of the first projects running on the Health Data Hub, aimed to identify real-life treatment regimens that could improve overall survival. The project is based on matching the national database of the sarcoma reference network with the SNDS.

objectivesWe aimed to report a transparent description of the linking process and its results.

methodsThe sarcoma database encompasses 33 548 patients matching the selection criteria divided into three subsets: 13507 patients with a complete dataset gathering clinical and pathological data; 5844 patients with clinical data alone; and 14 197 patients with pathological data alone. As no ICD-10 code reliably identifies patients with sarcoma, the subpopulation extracted from the SNDS was extended to 3 million patients who underwent surgery for their cancer. An indirect record linkage process used a combination (called a signature) of so-called chaining variables to uniquely identify a pair of patients from each of the bases. Two metrics (signature robustness and overall quality) were calculated for ease of interpretation.

resultsThe overall matching rate of 73.1% (24 539 pairs out of 33 548 observations), reaching 90.5% in the intersection of the sarcomas databases (with extended data, 12 225 pairs out of 13 507 observations).

conclusionAn optimized and transparent process led to a moderate matching rate but enhanced the confidence in true matching. Representativeness is an issue related to the missing data pattern across the three NETSARC databases. For instance, an individual present only in the RREPS database has a greater probability of not being linked.

Indexed as

Chemotherapy, AdjuvantDatabases, FactualMedical Record LinkageNeoadjuvant TherapySarcomaFranceHumansInformation Storage and Retrievaldata linkagehealth insurance reimbursementsarcoma

Identifiers

PMID41381053
PMCPMC12698291

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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 OpenQuestion graph.