Evidence map›Paper›PMID 27819858›Full record

ArticleClinical nuclear medicine2017

18F-FDG PET/CT Metabolic Tumor Volume and Intratumoral Heterogeneity in Pancreatic Adenocarcinomas: Impact of Dual-Time Point and Segmentation Methods.

Esther Mena, Sara Sheikhbahaei, Mehdi Taghipour, Abhinav K Jha, Esther Vicente, Jennifer Xiao, Rathan M Subramaniam

Abstract read
In one paragraph

Article in Clinical nuclear medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Need for objective task-based evaluation of AI-based segmentation methods for quantitative PET.Proceedings of SPIE--the International Society for Optical Engineering · 2023
    Article
  5. Diagnosis and prognostic predictive value of delineation methods fromAmerican journal of nuclear medicine and molecular imaging · 2023
    Article
  6. The prognostic value ofCancer imaging : the official publication of the International Cancer Imaging Society · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Development and validation of anEuropean radiology · 2020
    Article
  12. Article
  13. Article
  14. No-gold-standard evaluation of image-acquisition methods using patient data.Proceedings of SPIE--the International Society for Optical Engineering · 2017
    Article
  15. Article
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

7 authors.

Esther MenaFrom the *Russell H Morgan Department of Radiology and Radiological Sciences, Johns Hopkins School of Medicine, Baltimore, MD; and †Department of Radiology, and ‡Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX.
Sara Sheikhbahaei
Mehdi Taghipour
Abhinav K Jha
Esther Vicente
Jennifer Xiao
Rathan M Subramaniam

Funding

Multi-Modality Quantitiative Imaging for Evaluation of Response to Cancer TherapyU01CA140204 · NCI · JOHNS HOPKINS UNIVERSITY · PI DU, YONG, SOLNES, LILJA · 2011 to 2022
$6.1M
Quantitative SPECT for Targeted Radionuclide TherapyR01CA109234 · NCI · JOHNS HOPKINS UNIVERSITY · PI FREY, ERIC C. · 2006 to 2015
$4.2M
Training for Clinician Scientists in Imaging ResearchT32EB006351 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI POMPER, MARTIN G · 2006 to 2022
$4.0M
UT Southwestern NCI National Clinical Trials Network Lead Academic Site - U10U10CA180870 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC · 2014 to 2018
$3.4M
End-to-End Optimization of SPECT Instrumentation, Acquisition, and ReconstructionR01EB016231 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI FREY, ERIC C., LINKS, JONATHAN M. · 2013 to 2016
$1.4M
NCI NIH HHS R01 CA109234NCI NIH HHS U01 CA140204NCI NIH HHS U10 CA180870NIBIB NIH HHS R01 EB016231NIBIB NIH HHS T32 EB006351
6 · The paper itself

Abstract

objectivesWe aimed to determine the consistency of quantitative PET measurements of metabolic tumor volume (MTV) and intratumoral heterogeneity index for primary untreated pancreatic adenocarcinomas, when using dual-time point F-FDG PET/CT imaging.

methodsThis is an institutional review board-approved, retrospective study including 71 patients with pancreatic adenocarcinoma, who underwent dual-time point F-FDG PET/CT imaging, at approximately 1 hour (early) and 2 hours (delayed), after injection. Automated gradient-based and 50% SUVmax-threshold segmentation methods were used to assess the primary tumor MTV and metabolic intratumoral heterogeneity index, calculated as the area under cumulative SUV-volume histograms (AUC-CSH), with lower AUC-CHS indexes corresponding to higher degrees of tumor heterogeneity. We defined that more than a ±10% change in MTV or AUC-CSH, compared with baseline, as clinically significant.

resultsSeventy-one FDG-avid pancreatic tumors were identified, with an average tumor diameter of 3.4 ± 0.9 cm (range, 1.5-6.4 cm). Metabolic tumor volume values remained consistent between early and delayed imaging when using the gradient PET segmentation method (P = 0.086), whereas statistically significant change was seen when using 50% SUVmax-threshold segmentation (P < 0.001). A decrease in more than 10% change in MTV (% ΔMTV) was observed in 70.4% (50/71) tumors, and 7.0% (5/71) of the tumors showed an increase more than 10 % ΔMTV, when using the 50% SUVmax-threshold segmentation. AUC-CSH indexes showed statistically significant differences between early and delayed time points (P < 0.001), when using the gradient segmentation. AUC-CSH index decreased by 10% or greater in 40.8% (29/71) of the tumors. AUC-CSH index remained stable between early and delayed when using the 50% SUVmax-threshold segmentation (P = 0.148) with percentage of change of less than 10% for all tumors.

conclusionsMetabolic tumor volume was relatively stable between early and delayed time points when PET gradient segmentation was used but changed greater than 10% in 77.4% of the tumors at delayed time point when threshold segmentation was used. The tumor heterogeneity index (AUC-CSH) changed greater than 10% in 40.8% of tumors at delayed imaging, when gradient segmentation was used but remained stable when threshold segmentation was used. It is important to standardize uptake time and segmentation methods to use FDG PET MTV and heterogeneity index as imaging biomarkers.

Indexed as

AdenocarcinomaAgedAged, 80 and overArea Under CurveFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedPancreatic NeoplasmsPositron-Emission TomographyPositron Emission Tomography Computed TomographyRadiopharmaceuticalsRetrospective StudiesTumor BurdenFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID27819858
PMCPMC5360463

What OpenQuestion holds

Textmetadata
LicenceTDM
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.