Evidence map›Paper›PMID 36529498›Full record

ArticleMagnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine2024

Ex-vivo 1.5T MR Imaging versus CT in Estimating the Size of the Pathologically Invasive Component of Lung Adenocarcinoma Spectrum Lesions.

Daisuke Yamada, Masaki Matsusako, Daisuke Yoneoka, Katsunori Oikado, Hironori Ninomiya, Taiki Nozaki, Mitsutomi Ishiyama, Akari Makidono, Mizuto Otsuji, Harumi Itoh and 1 more

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Article in Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Daisuke YamadaDepartment of Radiology, St. Luke's International University.
Masaki MatsusakoDepartment of Radiology, St. Luke's International University.
Daisuke YoneokaInfectious Disease Surveillance Center, National Institute of Infectious Diseases.
Katsunori OikadoDiagnostic Imaging Center, The Cancer Institute Hospital of Japanese Foundation for Cancer Research.
Hironori NinomiyaDivision of Pathology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research.
Taiki NozakiDepartment of Radiology, St. Luke's International University.
Mitsutomi IshiyamaDiagnostic Imaging Center, The Cancer Institute Hospital of Japanese Foundation for Cancer Research.
Akari MakidonoDepartment of Diagnostic Radiology, Tokyo Metropolitan Children's Medical Center.
Mizuto OtsujiDepartment of Thoracic Surgery, Tokyo Metropolitan Bokutoh Hospital.
Harumi ItohDepartment of Radiology, Faculty of Medical Sciences, University of Fukui.
Hiroya OjiriDepartment of Radiology, The Jikei University School of Medicine and University Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of this study was to investigate whether ex-vivo MRI enables accurate estimation of the invasive component of lung adenocarcinoma.

methodsWe retrospectively reviewed 32 patients with lung adenocarcinoma who underwent lung lobectomy. The specimens underwent MRI at 1.5T. The boundary between the lesion and the normal lung was evaluated on a 5-point scale in each three MRI sequences, and a one-way analysis of variance and post-hoc tests were performed. The invasive component size was measured histopathologically. The maximum diameter of each solid component measured on CT and MR T1-weighted (T1W) images and the maximum size obtained from histopathologic images were compared using the Wilcoxon signed-rank test. Inter-reader agreement was evaluated using intraclass correlation coefficients (ICC).

resultsT1W images were determined to be optimal for the delineation of the lesions (P < 0.001). The histopathologic invasive area corresponded to the area where the T1W ex-vivo MR image showed a high signal intensity that was almost equal to the intravascular blood signal. The maximum diameter of the solid component on CT was overestimated compared with the maximum invasive size on histopathology (mean, 153%; P < 0.05), while that on MRI was evaluated mostly accurately without overestimation (mean, 108%; P = 0.48). The interobserver reliability of the measurements using CT and MRI was good (ICC = 0.71 on CT, 0.74 on MRI).

conclusionEx-vivo MRI was more accurate than conventional CT in delineating the invasive component of lung adenocarcinoma.

Indexed as

Adenocarcinoma of LungLung NeoplasmsHumansMagnetic Resonance ImagingReproducibility of ResultsRetrospective StudiesTomography, X-Ray Computedex-vivo magnetic resonance imaginginvasive componentlung adenocarcinomanoninvasive alveolar collapse

Identifiers

PMID36529498
PMCPMC10838715

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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.