Evidence map›Paper›PMID 36331867›Full record

ArticleThe British journal of surgery2022

Histopathological tumour response scoring in resected pancreatic cancer following neoadjuvant therapy: international interobserver study (ISGPP-1).

Boris V Janssen, Stijn van Roessel, Susan van Dieren, Onno de Boer, Volkan Adsay, Olca Basturk, Lodewijk Brosens, Fiona Campbell, Deyali Chatterjee, Angela Chou and 21 more

Open access · hybridAbstract read
In one paragraph

Article in The British journal of surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

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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

31 authors at 19 institutions in 10 countries.

Boris V JanssenDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Stijn van RoesselDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-3041-0452
Susan van DierenDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Onno de BoerDepartment of Pathology, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Volkan AdsayDepartment of Pathology, Koc University and KUTTAM Research Centre, Istanbul, Turkey.
Olca BasturkDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID 0000-0003-2747-1366
Lodewijk BrosensDepartment of Pathology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Fiona CampbellDepartment of Pathology, Royal Liverpool University Hospital, Liverpool, UK.
Deyali ChatterjeeDepartment of Anatomical Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Angela ChouCancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, and University of Sydney, Sydney, New South WalesAustralia.
Claudio DoglioniDepartment of Pathology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Irene EspositoInstitute of Pathology, Heinrich-Heine-University and University Hospital of Duesseldorf, Duesseldorf, Germany.
Roger FeakinsDepartment of Pathology, Royal Free London NHS Trust, London, UK.
Talia L FuchsCancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, and University of Sydney, Sydney, New South WalesAustralia.
Noriyoshi FukushimaDepartment of Pathology, Jichi Medical University Hospital, Tochigi, Japan.
Anthony J GillCancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, and University of Sydney, Sydney, New South WalesAustralia.
Seung-Mo HongDepartment of Pathology, Asan Medical Centre, Seoul, Korea.ORCID 0000-0002-8888-6007
Ralph H HrubanDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jeffrey KaplanDepartment of Pathology, University of Colorado Hospital, Denver, Colorado, USA.
Alyssa KrasinkasDepartment of Pathology, Emory University, Atlanta, Georgia, USA.
Claudio LuchiniDepartment of Diagnostics and Public Health, University and Hospital Trust of Verona, Verona, Italy.ORCID 0000-0003-4901-4908
Chanjuan ShiDepartment of Pathology, Duke University Medical Center, Durham, North Carolina, USA.
Aatur SinghiDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Elizabeth ThompsonDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Marie-Louise F VelthuysenDepartment of Pathology, Erasmus Medical Centre, Rotterdam, the Netherlands.ORCID 0000-0003-0435-9494
Marc G BesselinkDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0003-2650-9350
Joanne VerheijDepartment of Pathology, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Huamin WangDepartment of Anatomical Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Caroline VerbekeDepartment of Pathology, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Arantza FariñaDepartment of Pathology, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
International Study Group of Pancreatic Pathologists (ISGPP)
Amsterdam University Medical Centers · NLThe University of Sydney · AUJohns Hopkins University · USThe University of Texas MD Anderson Cancer Center · USAsan Medical Center · KRDuke Medical Center · USDüsseldorf University Hospital · DEEmory University · USErasmus University Rotterdam · NLJichi Medical University · JPKoç University · TRMemorial Sloan Kettering Cancer Center · USOslo University Hospital · NORoyal Free London NHS Foundation Trust · GBUniversity Medical Center Utrecht · NLUniversity of Colorado Hospital · USUniversity of Liverpool · GBUniversity of Pittsburgh · USVita-Salute San Raffaele University · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundMost tumour response scoring systems for resected pancreatic cancer after neoadjuvant therapy score tumour regression. However, whether treatment-induced changes, including tumour regression, can be identified reliably on haematoxylin and eosin-stained slides remains unclear. Moreover, no large study of the interobserver agreement of current tumour response scoring systems for pancreatic cancer exists. This study aimed to investigate whether gastrointestinal/pancreatic pathologists can reliably identify treatment effect on tumour by histology, and to determine the interobserver agreement for current tumour response scoring systems.

methodsOverall, 23 gastrointestinal/pancreatic pathologists reviewed digital haematoxylin and eosin-stained slides of pancreatic cancer or treated tumour bed. The accuracy in identifying the treatment effect was investigated in 60 patients (30 treatment-naive, 30 after neoadjuvant therapy (NAT)). The interobserver agreement for the College of American Pathologists (CAP) and MD Anderson Cancer Center (MDACC) tumour response scoring systems was assessed in 50 patients using intraclass correlation coefficients (ICCs). An ICC value below 0.50 indicated poor reliability, 0.50 or more and less than 0.75 indicated moderate reliability, 0.75 or more and below 0.90 indicated good reliability, and above 0.90 indicated excellent reliability.

resultsThe sensitivity and specificity for identifying NAT effect were 76.2 and 49.0 per cent respectively. After NAT in 50 patients, ICC values for both tumour response scoring systems were moderate: 0.66 for CAP and 0.71 for MDACC.

conclusionIdentification of the effect of NAT in resected pancreatic cancer proved unreliable, and interobserver agreement for the current tumour response scoring systems was suboptimal. These findings support the recently published International Study Group of Pancreatic Pathologists recommendations to score residual tumour burden rather than tumour regression after NAT.

Indexed as

Neoadjuvant TherapyPancreatic NeoplasmsEosine Yellowish-(YS)HumansObserver VariationReproducibility of ResultsEosine Yellowish-(YS)

Identifiers

PMID36331867
PMCPMC10364538
OpenAlexW4308189612

What OpenQuestion holds

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Registered trials

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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.