Evidence map›Paper›PMID 33266496›Full record

ReviewInternational journal of molecular sciences2020

Morphologic and Molecular Landscape of Pancreatic Cancer Variants as the Basis of New Therapeutic Strategies for Precision Oncology.

Chiara Bazzichetto, Claudio Luchini, Fabiana Conciatori, Vanja Vaccaro, Ilaria Di Cello, Paola Mattiolo, Italia Falcone, Gianluigi Ferretti, Aldo Scarpa, Francesco Cognetti and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  4. Intracholecystic papillary neoplasm mimicking a submucosal tumor.Clinical journal of gastroenterology · 2025
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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

11 authors.

Chiara BazzichettoMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-1648-3700
Claudio LuchiniDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.ORCID 0000-0003-4901-4908
Fabiana ConciatoriMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-8579-5222
Vanja VaccaroMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Ilaria Di CelloDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.
Paola MattioloDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, 37134 Verona, Italy.
Italia FalconeMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0003-2796-0792
Gianluigi FerrettiMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-2271-6427
Aldo ScarpaDepartment ARC-Net Research Centre, University and Hospital Trust of Verona, 37126 Verona, Italy.ORCID 0000-0003-1678-739X
Francesco CognettiMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Michele MilellaDivision of Oncology, University of Verona, 37126 Verona, Italy.

Funding

Fondazione AIRC per la ricerca sul cancro 23857IFO Sperimentazioni OM1 n.a.
6 · The paper itself

Abstract

To date, pancreatic cancer is still one of the most lethal cancers in the world, mainly due to the lack of early diagnosis and personalized treatment strategies. In this context, the possibility and the opportunity of identifying genetic and molecular biomarkers are crucial to improve the feasibility of precision medicine. In 2019, the World Health Organization classified pancreatic ductal adenocarcinoma cancer (the most common pancreatic tumor type) into eight variants, according to specific histomorphological features. They are: colloid carcinoma, medullary carcinoma, adenosquamous carcinoma, undifferentiated carcinoma, including also rhabdoid carcinoma, undifferentiated carcinoma with osteoclast-like giant cells, hepatoid carcinoma, and signet-ring/poorly cohesive cells carcinoma. Interestingly, despite the very low incidence of these variants, innovative high throughput genomic/transcriptomic techniques allowed the investigation of both somatic and germline mutations in each specific variant, paving the way for their possible classification according also to specific alterations, along with the canonical mutations of pancreatic cancer (

Indexed as

MutationPrecision MedicineCarcinoma, Pancreatic DuctalGenomicsGerm-Line MutationHumansNeoplasm ProteinsPancreatic NeoplasmsNeoplasm Proteinsgenetic statushistologymolecular alterationpancreatic cancerprecision medicinevariants

Identifiers

PMID33266496
PMCPMC7700259

What OpenQuestion holds

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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.