Evidence map›Paper›PMID 39664608›Full record

ArticleFrontiers in nuclear medicine2024

Immunohistochemical basis for FAP as a candidate theranostic target across a broad range of cholangiocarcinoma subtypes.

Laura C Jorgenson, Michael S Torbenson, Thorvardur R Halfdanarson, Lionel A Kankeu Fonkoua, Nguyen H Tran, Lewis R Roberts, Rory L Smoot, Ajit H Goenka, Scott M Thompson

Abstract read
In one paragraph

Article in Frontiers in nuclear medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. [EJNMMI research · 2025
    Article
  2. Review
  3. 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

9 authors.

Laura C JorgensonDepartment of Radiology, Mayo Clinic, Rochester, MN, United States.
Michael S TorbensonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Thorvardur R HalfdanarsonDivision of Medical Oncology, Mayo Clinic, Rochester, MN, United States.
Lionel A Kankeu FonkouaDivision of Medical Oncology, Mayo Clinic, Rochester, MN, United States.
Nguyen H TranDivision of Medical Oncology, Mayo Clinic, Rochester, MN, United States.
Lewis R RobertsDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Rory L SmootDivision of Hepatobiliary and Pancreas Surgery, Mayo Clinic, Rochester, MN, United States.
Ajit H GoenkaDepartment of Radiology, Mayo Clinic, Rochester, MN, United States.
Scott M ThompsonDepartment of Radiology, Mayo Clinic, Rochester, MN, United States.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
Optimizing Pancreatic Cancer Management with Next Generation Imaging and Liquid BiopsyR01CA256969 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Collisson, Ajit Harishkumar Goenka · 2021 to 2026
$3.1M
Quantitative In Vivo 68Ga-Fibroblast-Activation-Protein-Inhibitors (FAPI)-46 PET Imaging of Cancer-Associated Fibroblasts (CAFs) in Pancreatic Ductal Adenocarcinoma (PDA)R01CA272628 · NCI · MAYO CLINIC ROCHESTER · PI GOENKA, AJIT HARISHKUMAR · 2022 to 2025
$2.5M
NCI NIH HHS P30 CA015083NCI NIH HHS R01 CA256969NCI NIH HHS R01 CA272628
6 · The paper itself

Abstract

Purpose: The aims of this study were to evaluate and compare fibroblast activation protein (FAP) expression and localization in surgically resected cholangiocarcinoma (CCA), primary and metastatic hepatocellular carcinoma (HCC), hepatocellular adenoma (HCA), and focal nodular hyperplasia (FNH), and to identify any association between CCA clinical or pathologic features and FAP expression. Materials and methods: FAP immunostaining from surgically resected CCA ( Results: Moderate-strong FAP expression in the tumor stroma was present in 93.1% of CCA, 60.7% of extrahepatic metastatic HCC, 29.6% of primary HCC, 21.1% of FNH, and 11.6% of HCA. Moderate-strong FAP expression in tumor stroma was significantly more prevalent in CCA than HCC ( Conclusion: FAP is expressed in the stroma of a high proportion (93%) of primary CCA independent of patient clinical or tumor pathology features. As such, these data provide the tissue basis for systematically evaluating FAP as a theranostic target across a broad range of CCA subtypes.

Indexed as

cholangiocarcinoma (CCA)fibroblast activation protein (FAP)liver neoplasmsprecision medicinetheranostics

Identifiers

PMID39664608
PMCPMC11631625

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.