Evidence map›Paper›PMID 40499590›Full record

ArticleJournal of the National Comprehensive Cancer Network : JNCCN2025

Histologic- and Genomic-Directed Adjuvant Therapy for Ampullary Adenocarcinoma: A Hidden Genome-Derived Analysis.

Brett L Ecker, Kenneth Seier, Ankur Choubey, Austin M Eckhoff, Gabriella N Tortorello, Vinod P Balachandran, Nicola Blackburn, Michael I D'Angelica, Ronald P DeMatteo, Daniel G Blazer and 19 more

Abstract read
In one paragraph

Article in Journal of the National Comprehensive Cancer Network : JNCCN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Rare, Yet Targetable: New Perspectives on Ampullary Carcinomas.International journal of molecular sciences · 2026
    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

29 authors.

Brett L Ecker1Division of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ.
Kenneth Seier2Department of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Ankur Choubey3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Austin M Eckhoff4Department of Surgery, Duke University School of Medicine, Durham, NC.
Gabriella N Tortorello5Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Vinod P Balachandran3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Nicola Blackburn6The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
Michael I D'Angelica3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Ronald P DeMatteo5Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Daniel G Blazer4Department of Surgery, Duke University School of Medicine, Durham, NC.
Jeffrey A Drebin3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
William E Fisher7Department of Surgery, Baylor College of Medicine, Houston, TX.
Anthony J Gill6The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
Marie-Claude Gingras10Department of Human and Molecular Genetics, Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX.
T Peter Kingham3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Major K Lee5Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Michael E Lidsky4Department of Surgery, Duke University School of Medicine, Durham, NC.
Daniel P Nussbaum4Department of Surgery, Duke University School of Medicine, Durham, NC.
Michael J Overman11Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Jaswinder S Samra8Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Ronglai Shen2Department of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Carlie S Sigel12Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Charles M Vollmer5Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Alice C Wei3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Sabino Zani4Department of Surgery, Duke University School of Medicine, Durham, NC.
Australian Pancreatic Genome Initiative6The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
Robert E Roses5Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Mithat Gonen2Department of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
William R Jarnagin3Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, NY.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Improving Outcome in Patients with Advanced Intrahepatic Cholangiocarcinoma: A Randomized Phase II Study of Gemcitabine and Oxaliplatin With or Without Regional Floxuridine (FUDR)U01CA238444 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CERCEK, ANDREA, IACOBUZIO-DONAHUE, CHRISTINE A · 2020 to 2024
$3.3M
NCI NIH HHS P30 CA008748NCI NIH HHS U01 CA238444
6 · The paper itself

Abstract

backgroundThe benefit of adjuvant chemotherapy (AC) for ampullary adenocarcinoma is unclear. The Hidden Genome model classifies prognostic subtypes with greater accuracy than standard histologic classification (intestinal [INT] vs pancreatobiliary [PB]), but its predictive capacity to guide the use of AC remains unstudied.

methodsWe applied the Hidden Genome model to an international cohort of 183 patients with resected ampullary adenocarcinoma who underwent genomic sequencing. The model quantified the predicted cell of origin (colorectal vs pancreas/distal bile duct) in all specimens. Overall survival (OS) was compared using Kaplan-Meier estimates, stratified by AC use versus surgery alone (SA).

resultsMost patients (n=128; 69.9%) received AC, which was not associated with a significant improvement in OS (median, 50.9 months [95% CI, 36.5-76.9] vs 53.8 months [95% CI, 32.4-119.0]; P=.816). Histologic subtype was neither associated with prognosis (P=.241) nor predictive of chemotherapy efficacy for INT-subtype (P=.379) or PB-subtype (P=.544) tumors. When stratified by genomic subtype, the colorectal group had a favorable prognosis regardless of AC use (median OS, 74.4 months [95% CI, 33.8-97.8] for AC vs 98.7 months [95% CI, 32.4-140.9] for SA; P=.889). Among patients with pancreas/distal bile duct tumors, those who received AC had longer survival compared with those who underwent SA (78.2 months [9.8-not reached] vs 22.7 months [2.3-not reached], respectively; hazard ratio, 0.17 [95% CI, 0.04-0.80]; P=.024).

conclusionsAC regimens were not associated with improved survival in histologically defined INT- or PB-subtype ampullary adenocarcinoma. However, genomic classification better stratified risk groups and identified patients more likely to benefit from AC.

Indexed as

AdenocarcinomaAmpulla of VaterCommon Bile Duct NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorChemotherapy, AdjuvantFemaleGenomicsHumansMaleMiddle AgedPrognosisBiomarkers, Tumor

Identifiers

PMID40499590
PMCPMC13012081

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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.