Evidence map›Paper›PMID 42541517›Full record

Observational studyFamilial cancer2026

Mainstream and fast-track genetic testing in pancreatic cancer patients and its impact on treatment: our experience in a tertiary hospital in Spain.

M Bringas, I Echavarría, C Polo, N Jiménez-Alduán, C Flores, A Muñoz, L Ortega, G Torres, J Soto-Alsar, A Calvo and 8 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Familial cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

18 authors.

M BringasMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain. m.bringasberanek@gmail.com.ORCID 0000-0001-8266-705X
I EchavarríaMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
C PoloMedical Oncology Service, HGUGM, IiSGM, Madrid, Spain.
N Jiménez-AlduánMedical Oncology Service, HGUGM, IiSGM, Madrid, Spain.
C FloresMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
A MuñozMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
L OrtegaMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
G TorresMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
J Soto-AlsarMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
A CalvoMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
P García AlfonsoMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
J A PajaresGastroenterology Service, HGUGM, Madrid, Spain.
J Suárez-GonzálezGenomic Unit, HGUGM and IiSGM, Madrid, Spain.
M Del Monte-MillánMedical Oncology Service, HGUGM, IiSGM, Madrid, Spain.
Tatiana MassarrahMedical Oncology Service, HGUGM, IiSGM, Madrid, Spain.
F Ayala de la PeñaMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
M MartínMedical Oncology Service, GEICAM, HGUGM, Universidad Complutense, IiSGM, Madrid, Spain.
I Márquez-RodasMedical Oncology Department, Hospital General Universitario Gregorio Marañón (HGUGM), Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PC) is a highly lethal malignancy. 4-10% are linked to inherited mutations in genes such as BRCA1/2, PALB2, ATM and mismatch repair (MMR) genes. Germline testing is essential to guide treatment decisions, yet delays remain common. Genetic testing models without pre-test assessment in a Hereditary Cancer Unit (HCU), have emerged as a strategy to improve earlier clinical decision-making. A retrospective, observational and descriptive study was conducted on 223 PC patients (55% male; average age 64 years) who underwent rapid germline genetic testing at Hospital General Universitario Gregorio Marañón (Madrid, Spain) between April 2019 and May 2024. Tests were ordered by oncologists with brief pre-test counseling, followed by a nurse-facilitated consent and peripheral blood collection. Post-test counseling in an HCU was offered for patients with variants of unknown significance (VUS) and pathogenic/likely pathogenic variants (PV), or upon physician or patient request. PV and VUS were identified in 32 (14.3%) and 82 (36.7%) patients, respectively. 50% of PV carriers did not meet familial PC criteria. Actionable mutations were detected in 14 (43.7%) of PV carriers, involving BRCA2 (6/32), PALB2 (1/32) and ATM (7/32). Treatment modifications occurred in 7/223 patients (3%), including PARP inhibitors or platinum-based regimens. Median time from the genetic test request to the results was 48 days (95% CI, 44-52). Mainstream genetic testing in PC is a viable approach to expedite results and facilitate precision oncology. Further studies are needed to evaluate long-term outcomes, cost-effectiveness and the psychosocial impact compared to traditional genetic counseling pathways.

Indexed as

Genetic TestingPancreatic NeoplasmsAdultAgedAtaxia Telangiectasia Mutated ProteinsBRCA2 ProteinFanconi Anemia Complementation Group N ProteinFemaleGenetic CounselingGenetic Predisposition to DiseaseGerm-Line MutationHumansMaleMiddle AgedRetrospective StudiesSpainAtaxia Telangiectasia Mutated ProteinsBRCA2 ProteinFanconi Anemia Complementation Group N ProteinPALB2 protein, humangermline genetic testinghereditary cancerMainstreamingpancreatic cancerprecision oncology

Identifiers

What OpenQuestion holds

Textmetadata
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.