Evidence map›Paper›PMID 30697457›Full record

ArticleAmerican journal of nuclear medicine and molecular imaging2018

Multi-level otsu method to define metabolic tumor volume in positron emission tomography.

Hyung-Jun Im, Meiyappan Solaiyappan, Inki Lee, Tyler Bradshaw, Najat C Daw, Fariba Navid, Barry L Shulkin, Steve Y Cho

Abstract read
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Article in American journal of nuclear medicine and molecular imaging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Hyung-Jun ImRadiology, University of Wisconsin Madison, WI, USA.
Meiyappan SolaiyappanRadiology, Johns Hopkins School of Medicine Baltimore, MD, USA.
Inki LeeRadiology, University of Wisconsin Madison, WI, USA.
Tyler BradshawMedical Physics, University of Wisconsin Madison, WI, USA.
Najat C DawDivision of Pediatrics, MD Anderson Cancer Center Houston, TX, USA.
Fariba NavidDepartment of Pediatrics, Children's Hospital Los Angeles Los Angeles, CA, USA.
Barry L ShulkinDepartment of Diagnostic Imaging, St. Jude Children's Research Hospital Memphis, TN, USA.
Steve Y ChoRadiology, University of Wisconsin Madison, WI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was to validate reliability and clinical utility of a PET tumor segmentation method using multi-level Otsu (MO-PET) in standard National Electrical Manufacturers Association (NEMA) image quality (IQ) phantom and patients with osteosarcoma. The NEMA IQ phantom was prepared with a lesion-to-background ratio (LBR) of either 8:1, 4:1, or 1.5:1. The artificial lesions in the phantom were segmented using MO-PET, gradient-based method (PETedge), relative threshold methods, and background threshold methods. Metabolic tumor volumes (MTVs) using MO-PET and PETedge were named as MTV (MO-PET) and MTV (PETedge), respectively. Among the MTVs using multiple methods, only MTV (MO-PET) and MTV (PETedge) showed excellent agreements with the actual volume of NEMA IQ phantom across the different LBRs (intraclass correlation coefficient, ICC = 0.987, 0.985 in LBR 8:1, 0.981, 0.993 in LBR 4:1 and 0.947, 0.994 in LBR 1.5:1). Repeated measurements of MTV (MO-PET) of the primary tumors showed excellent reproducibility with ICC of 0.994 (0.989-0.997) in patients with osteosarcoma. Also, MTV (MO-PET) was found to be predictive of Event Free Survival (EFS) [Hazard ratio (95% CI) = 6.1 (2.1-17.2), log rank P = 0.0003] in patients with osteosarcoma. We have validated in NEMA IQ phantom that the MTV (MO-PET) is accurate, and importantly, stable and consistent across a range of lesion sizes and LBRs representative of clinical tumor lesions. Furthermore, MTV (MO-PET) showed excellent reproducibility and was predictive for EFS in patients with osteosarcoma.

Indexed as

18F-fluorodeoxyglucosemetabolic tumor volumeMulti-level otsupositron emission tomographysegmentation

Identifiers

PMID30697457
PMCPMC6334209

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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.