Evidence map›Paper›PMID 24440063›Full record

ArticleJournal of the American College of Surgeons2014

Assessment of tumor growth in pancreatic neuroendocrine tumors in von Hippel Lindau syndrome.

Allison B Weisbrod, Mio Kitano, Francine Thomas, David Williams, Neelam Gulati, Krisana Gesuwan, Yixun Liu, David Venzon, Ismail Turkbey, Peter Choyke and 5 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of the American College of Surgeons, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Belzutifan for von Hippel-Lindau Disease: Pancreatic Lesion Population of the Phase 2 LITESPARK-004 Study.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Inherited syndromes involving pancreatic neuroendocrine tumors.Journal of gastrointestinal oncology · 2020
    Review
  12. Article
  13. Review
  14. Pancreatic necrosis: Complications and changing trend of treatment.World journal of gastrointestinal surgery · 2019
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Von Hippel-Lindau disease.Handbook of clinical neurology · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 1 country.

Allison B WeisbrodEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Mio KitanoEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Francine ThomasDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
David WilliamsDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Neelam GulatiEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Krisana GesuwanEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Yixun LiuDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
David VenzonBiostatistics and Data Management Section, Office of the Clinical Director, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Ismail TurkbeyDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Peter ChoykeDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Jack YaoDiagnostic Radiology Department, Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Steven K LibuttiDepartment of Surgery, Montefiore Medical Center and the Albert Einstein College of Medicine, Bronx, NY.
Naris NilubolEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
William M LinehanUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Electron KebebewEndocrine Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD. Electronic address: kebebewe@mail.nih.gov.
National Cancer Institute · USNational Institutes of Health · USAlbert Einstein College of Medicine · USNational Institutes of Health Clinical Center · US

Funding

Molecular Therapeutics of Kidney Cancer: VHL Gene and Fumarate Hydratase GeneZIABC011038 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LINEHAN, WILLIAM MARSTON · 2009 to 2025
$29.8M
Clinical Studies of the Molecular Genetic Basis of Kidney CancerZIABC011028 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LINEHAN, WILLIAM MARSTON · 2009 to 2025
$17.9M
Clinical Nursing and Data Management CoreZIDBC011089 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LINEHAN, WILLIAM MARSTON · 2009 to 2025
$17.4M
Office of Collaborative BiostatisticsZIDSC007202 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI CHOO-WOSOBA, HYOYOUNG · 2009 to 2025
$14.5M
Clinical Image Processing ServiceZIDCL040016 · CLC · CLINICAL CENTER · PI SUMMERS, RONALD M. · 2012 to 2014
$0k
Intramural NIH HHS Z99 CA999999NCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

backgroundThe incidence of pancreatic neuroendocrine tumors (PNETs) is increasing, but only a subset of these heterogeneous tumors will progress to malignant disease, which is associated with a poor prognosis. Currently, there are limited data on the natural history of these tumors and it is difficult to determine which patients require surgical intervention because the risk of metastatic disease cannot be accurately determined. STUDY

designWe conducted a prospective study of 87 patients with von Hippel Lindau syndrome-associated solid pancreatic lesions to determine the natural history of these tumors with biochemical testing, follow-up anatomic and functional imaging, and advanced imaging analysis, with a median follow-up of 4 years.

resultsApproximately 20% of consecutive tumor measurements during follow-up were decreased in size and 20% showed no change. This included 2 of 4 surgically proven malignant tumors, which had a net decrease in tumor size over time. Tumor volume, as derived from greatest diameter and volumetric measurements, showed good correlation to pathology tumor measurement of surgically resected tumors (Spearman rank correlation ρ = 0.72, p = 0.0011, and ρ = 0.83, p < 0.0001, respectively). Tumor density measurement had an inverse relationship with tumor size (Spearman rank correlation -0.22, p = 0.0047). A tumor density cutoff of 200 was 75% specific for malignant tumors.

conclusionsPancreatic neuroendocrine tumors demonstrate a nonlinear growth pattern, which includes periods of no growth and apparent decrease in size by imaging. These growth patterns are variable and are not associated with tumor grade and malignancy. Tumor density, as measured in this cohort, may offer a specific diagnostic tool for malignant disease.

Indexed as

Diagnosis, DifferentialDisease ProgressionFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedNeuroendocrine TumorsPancreatic NeoplasmsProspective StudiesTomography, X-Ray Computedvon Hippel-Lindau DiseaseCgAchromogranin Apancreatic neuroendocrine tumorpancreatic polypeptidePNETPPPVHLvon Hippel Lindau syndrome

Identifiers

PMID24440063
PMCPMC3896892
OpenAlexW2062682629

What OpenQuestion holds

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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.