Evidence map›Paper›PMID 33528694›Full record

ArticleMedical oncology (Northwood, London, England)2021

Extensive molecular reclassification: new perspectives in small bowel adenocarcinoma?

Andrea Casadei-Gardini, Sara Lonardi, Valeria Smiroldo, Matteo Canale, Alessandro Passardi, Nicola Silvestris, Giulia Orsi, Floriana Nappo, Lorenza Rimassa, Matteo Fassan and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2021. 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
0.5field-weighted citation impact, top 37% 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.

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, 4 citations in OpenAlex.

  1. Article
  2. Review
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

14 authors at 7 institutions in 1 country.

Andrea Casadei-GardiniDepartment of Medical Oncology, Università Vita-Salute San Raffaele, IRCCS-Ospedale San Raffaele, Via Olgettina 70, 20132, Milan, Italy. casadeigardini@gmail.com.ORCID http://orcid.org/0000-0001-6289-7202
Sara LonardiEarly Phase Clinical Trial Unit, Department of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Valeria SmiroldoMedical Oncology and Hematology Unit, Humanitas Cancer Center; IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Matteo CanaleBiosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori", 47014, Meldola, Italy.
Alessandro PassardiDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori", Meldola, Italy.
Nicola SilvestrisMedical Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, Bari, Italy.
Giulia OrsiDepartment of Medical Oncology, Università Vita-Salute San Raffaele, IRCCS-Ospedale San Raffaele, Via Olgettina 70, 20132, Milan, Italy.
Floriana NappoMedical Oncology Unit 1, Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Lorenza RimassaMedical Oncology and Hematology Unit, Humanitas Cancer Center; IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Matteo FassanDepartment of Medicine (DIMED), Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.
Paola SpaggiariDepartment of Pathology, IRCCS Humanitas Research Hospital, Milan, Italy.
Oronzo BrunettiMedical Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, Bari, Italy.
Kalliopi AndrikouDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori", Meldola, Italy.
Stefano CascinuDepartment of Medical Oncology, Università Vita-Salute San Raffaele, IRCCS-Ospedale San Raffaele, Via Olgettina 70, 20132, Milan, Italy.
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITVita-Salute San Raffaele University · ITHumanitas University · ITIstituto Tumori Bari · ITUniversity of Padua · ITIRCCS Humanitas Research Hospital · ITIstituto Oncologico Veneto · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SBA classification is still based on the location of the primary tumor, without genetic information. in the current study, an extensive genetic profile of SBA, was performed in order to identify and quantify targetable alterations for a future precision medicine in SBA. Clinical-pathological information for 24 patients affected by SBA were retrospectively reviewed. Whole genome analysis of the primary tumors was performed by the FOUNDATION Cdx technology. We carried out a functional enrichment analysis of the mutated genes with BioPlanet. Integrative clustering analysis revealed three distinct subtypes characterized by different genomic alterations. Cluster 1exhibited significant correlations with MSI status, high TMB, celiac disease and Jejunual site.We defined cluster 1 as "immunological subtype" (29.2% of patients). Driver mutations in this subtype suggest that 100% of patients may benefit from immunotherapy. Enrichment analysis of cluster 2 highlighted that the main affected pathway was that of homologous DNA pairing and strand exchange (16.7% of patients). We defined this cluster as "DNA Damage Repair (DDR) like". On the basis of these driver molecular alterations, 100% of patients could benefit from PARPi. Finally, Cluster 3 had no significant correlations with clinical-pathological characteristics (54.1% of patients). Enrichment analysis revealed that this cluster has remarkable similarities with CRA genomic profile, so we defined it as "Colon-like". SBA is a genetically distinct tumor entity and deep mutation heterogeneity indicates that different driver genes play a role in the biology of these tumors. The identification of clusters based on genetic profile suggest the possibility to go beyond chemotherapy in several patients.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overCluster AnalysisDNA RepairDuodenal NeoplasmsFemaleHumansIntestinal NeoplasmsIntestine, SmallMaleMicrosatellite InstabilityMiddle AgedMutationRetrospective StudiesATMBRCACeliac diseaseImmunotherapyMicrosatellite instabilityMolecularNF43ParpiTumor mutational burden

Identifiers

PMID33528694
OpenAlexW3127030577

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.