Evidence map›Paper›PMID 34613461›Full record

ArticleVirchows Archiv : an international journal of pathology2022

Histo-molecular characterization of pancreatic cancer with microsatellite instability: intra-tumor heterogeneity, B2M inactivation, and the importance of metastatic sites.

Claudio Luchini, Andrea Mafficini, Deyali Chatterjee, Maria L Piredda, Concetta Sciammarella, Pooja Navale, Giuseppe Malleo, Paola Mattiolo, Giovanni Marchegiani, Antonio Pea and 10 more

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Research progress in diagnosis and treatment of pancreatic cancer with mismatch repair and microsatellite instability.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

20 authors at 7 institutions in 4 countries.

Claudio LuchiniDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy. claudio.luchini@univr.it.ORCID http://orcid.org/0000-0003-4901-4908
Andrea MafficiniDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
Deyali ChatterjeeDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Maria L PireddaARC-Net Research Center, University and Hospital Trust of Verona, Verona, Italy.
Concetta SciammarellaARC-Net Research Center, University and Hospital Trust of Verona, Verona, Italy.
Pooja NavaleDepartment of Pathology and Immunology, Washington University, St. Louis, MO, USA.
Giuseppe MalleoDepartment of Surgery, The Pancreas Institute, University and Hospital Trust of Verona, Verona, Italy.
Paola MattioloDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
Giovanni MarchegianiDepartment of Pathology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Antonio PeaIRCCS Istituto Tumori "Giovanni Paolo II" of Bari, and Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Bari, Italy.
Roberto SalviaDepartment of Surgery, The Pancreas Institute, University and Hospital Trust of Verona, Verona, Italy.
Lodewijk A BrosensDepartment of Pathology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Gaetano PaolinoDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
Maria G MastrosiminiDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
Nicola SilvestrisIRCCS Istituto Tumori "Giovanni Paolo II" of Bari, and Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Bari, Italy.
Michele MilellaDepartment of Medicine, Section of Oncology, University and Hospital Trust of Verona, Verona, Italy.
Liang ChengDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Volkan N AdsayDepartment of Pathology, Koç University Hospitals, Istanbul, Turkey.
Rita T LawlorARC-Net Research Center, University and Hospital Trust of Verona, Verona, Italy.
Aldo ScarpaDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Piazzale Scuro, 10, 37134, Verona, Italy. aldo.scarpa@univr.it.
University of Verona · ITIstituto Tumori Bari · ITRadboud University Nijmegen · NLIndiana University School of MedicineKoç University · TRThe University of Texas MD Anderson Cancer Center · USWashington University in St. Louis · US

Funding

associazione italiana per la ricerca sul cancro 12182fondazione cariverona: oncology biobank project "antonio schiavi" 203885/2017fondazione italiana malattie pancreas J38D19000690001italian ministry of health RF CO-2019-12369662: CUP: B39C21000370001
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) with microsatellite instability (MSI)/defective mismatch repair (dMMR) is the only subtype of pancreatic cancer with potential response to immunotherapy. Here, we report the histo-molecular characterization of MSI/dMMR PDAC with immunohistochemistry, MSI-based PCR, and next-generation sequencing. Five paradigmatic cases have been identified. The main results include the first report in pancreatic cancer of MSI/dMMR intra-tumor heterogeneity, the presence of microsatellite-stable metastases from MSI/dMMR primary and recurrent B2M gene inactivation, which may confer resistance to immunotherapy. In addition to the classic PDAC drivers, ARID1A was the most common mutated gene in the cohort. Intra-tumor heterogeneity, B2M inactivation, and metastatic sites should be carefully considered in MSI/dMMR PDAC, which should also be investigated in routine diagnostic practice with specific molecular analysis. The chromatin remodeler ARID1A represents another potential driver gene in this context.

Indexed as

Carcinoma, Pancreatic DuctalColorectal NeoplasmsPancreatic NeoplasmsDNA Mismatch RepairHumansMicrosatellite InstabilityB2MImmunotherapyMicrosatellitePancreatic cancerPancreatic ductal adenocarcinoma

Identifiers

PMID34613461
OpenAlexW3202242856

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.