Evidence map›Paper›PMID 32181445›Full record

ArticleJHEP reports : innovation in hepatology2020

Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine.

Jennifer L Leiting, Stephen J Murphy, John R Bergquist, Matthew C Hernandez, Tommy Ivanics, Amro M Abdelrahman, Lin Yang, Isaac Lynch, James B Smadbeck, Sean P Cleary and 7 more

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Guideline
  2. Utilizing Patient-Derived Xenografts to Model Precision Oncology for Biliary Tract Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  3. Article
  4. Article
  5. Generation of Metastatic Cholangiocarcinoma Patient-Derived Xenograft Models.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Article
  7. Human Metastatic Cholangiocarcinoma Patient-Derived Xenografts and Tumoroids for Preclinical Drug Evaluation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Overview of current targeted therapy in gallbladder cancer.Signal transduction and targeted therapy · 2020
    Review
  16. In Vivo Models for Cholangiocarcinoma-What Can We Learn for Human Disease?International journal of molecular sciences · 2020
    Review
  17. The second volume.JHEP reports : innovation in hepatology · 2020
    Article
  18. 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

17 authors at 3 institutions in 1 country.

Jennifer L LeitingDepartment of Surgery, Mayo Clinic, Rochester, MN.
Stephen J MurphyCenter for Individualized Medicine, Mayo Clinic, Rochester, MN.
John R BergquistDepartment of Surgery, Mayo Clinic, Rochester, MN.
Matthew C HernandezDepartment of Surgery, Mayo Clinic, Rochester, MN.
Tommy IvanicsDepartment of Surgery, Henry Ford Medical Center, Detroit, MI.
Amro M AbdelrahmanDepartment of Surgery, Mayo Clinic, Rochester, MN.
Lin YangCenter for Individualized Medicine, Mayo Clinic, Rochester, MN.
Isaac LynchDepartment of Surgery, Mayo Clinic, Rochester, MN.
James B SmadbeckCenter for Individualized Medicine, Mayo Clinic, Rochester, MN.
Sean P ClearyDepartment of Surgery, Mayo Clinic, Rochester, MN.
David M NagorneyDepartment of Surgery, Mayo Clinic, Rochester, MN.
Michael S TorbensonDepartment of Pathology, Mayo Clinic, Rochester, MN.
Rondell P GrahamDepartment of Pathology, Mayo Clinic, Rochester, MN.
Lewis R RobertsDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.
Gregory J GoresDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.
Rory L SmootDepartment of Surgery, Mayo Clinic, Rochester, MN.
Mark J TrutyDepartment of Surgery, Mayo Clinic, Rochester, MN.
Mayo Clinic in Arizona · USMayo Clinic · USHenry Ford Hospital · US

Funding

Project 4: ImmunovirotherapyP50CA210964 · NCI · MAYO CLINIC ROCHESTER · PI Rory Smoot · 2018 to 2026
$20.5M
NCI NIH HHS P50 CA210964
6 · The paper itself

Abstract

BACKGROUND &

aimsBiliary tract tumors are uncommon but highly aggressive malignancies with poor survival outcomes. Due to their low incidence, research into effective therapeutics has been limited. Novel research platforms for pre-clinical studies are desperately needed. We sought to develop a patient-derived biliary tract cancer xenograft catalog.

methodsWith appropriate consent and approval, surplus malignant tissues were obtained from surgical resection or radiographic biopsy and implanted into immunocompromised mice. Mice were monitored for xenograft growth. Established xenografts were verified by a hepatobiliary pathologist. Xenograft characteristics were correlated with original patient/tumor characteristics and oncologic outcomes. A subset of xenografts were then genomically characterized using Mate Pair sequencing (MPseq).

resultsBetween October 2013 and January 2018, 87 patients with histologically confirmed biliary tract carcinomas were enrolled. Of the 87 patients, 47 validated PDX models were successfully generated. The majority of the PDX models were created from surgical resection specimens (n = 44, 94%), which were more likely to successfully engraft when compared to radiologic biopsies (

conclusionsThis is the largest series of biliary tract cancer xenografts reported to date. Histologic and genomic analysis of patient-derived xenografts demonstrates accurate recapitulation of original tumor morphology with direct correlations to patient outcomes. Successful development of biliary cancer tumografts is feasible and may be used to direct subsequent therapy in high recurrence risk patients. LAY SUMMARY: Patient biliary tract tumors grown in immunocompromised mice are an invaluable resource in the treatment of biliary tract cancers. They can be used to guide individualized cancer treatment in high-risk patients.

Indexed as

biliary tractCCA, cholangiocarcinomacholangiocarcinomadCCA, distal cholangiocarcinomaECM, extracellular matrixgallbladder carcinomaGBCA, gallbladder carcinomaHRs, hazard ratiosiCCA, intrahepatic cholangiocarcinomaLOH, loss of heterozygosityMatePair sequencingOPTR, overall patient take rateOS, overall survivalPatient-derived xenograftspCCA, perihilar cholangiocarcinomaPDX, patient-derived xenograftTTF, time to tumor formationTTH, time to tumor harvest

Identifiers

PMID32181445
PMCPMC7066236
OpenAlexW2999277579

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.