Evidence map›Paper›PMID 32057115›Full record

ArticleMagnetic resonance in medicine2020

Diffusion model comparison identifies distinct tumor sub-regions and tracks treatment response.

Damien J McHugh, Grazyna Lipowska-Bhalla, Muhammad Babur, Yvonne Watson, Isabel Peset, Hitesh B Mistry, Penny L Hubbard Cristinacce, Josephine H Naish, Jamie Honeychurch, Kaye J Williams and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Magnetic resonance in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Damien J McHughQuantitative Biomedical Imaging Laboratory, The University of Manchester, Manchester, UK.ORCID 0000-0002-1446-5883
Grazyna Lipowska-BhallaQuantitative Biomedical Imaging Laboratory, The University of Manchester, Manchester, UK.
Muhammad BaburDivision of Pharmacy & Optometry, The University of Manchester, Manchester, UK.
Yvonne WatsonQuantitative Biomedical Imaging Laboratory, The University of Manchester, Manchester, UK.
Isabel PesetImaging and Flow Cytometry, Cancer Research UK Manchester Institute, Manchester, UK.
Hitesh B MistryDivision of Cancer Sciences, The University of Manchester, Manchester, UK.
Penny L Hubbard CristinacceDivision of Cardiovascular Sciences, The University of Manchester, Manchester, UK.
Josephine H NaishDivision of Cardiovascular Sciences, The University of Manchester, Manchester, UK.
Jamie HoneychurchDivision of Cancer Sciences, The University of Manchester, Manchester, UK.
Kaye J WilliamsDivision of Pharmacy & Optometry, The University of Manchester, Manchester, UK.
James P B O'ConnorQuantitative Biomedical Imaging Laboratory, The University of Manchester, Manchester, UK.
Geoffrey J M ParkerBioxydyn Ltd., Manchester, UK.ORCID 0000-0003-2934-2234
University of Manchester · GBCancer Research UK Manchester Institute · GB

Funding

Cancer Research UK 16465Cancer Research UK C147/A25254Cancer Research UK C19221/A22746Cancer Research UK C19221/A28683Cancer Research UK C8742/A18097
6 · The paper itself

Abstract

purposeMRI biomarkers of tumor response to treatment are typically obtained from parameters derived from a model applied to pre-treatment and post-treatment data. However, as tumors are spatially and temporally heterogeneous, different models may be necessary in different tumor regions, and model suitability may change over time. This work evaluates how the suitability of two diffusion-weighted (DW) MRI models varies spatially within tumors at the voxel level and in response to radiotherapy, potentially allowing inference of qualitatively different tumor microenvironments.

methodsDW-MRI data were acquired in CT26 subcutaneous allografts before and after radiotherapy. Restricted and time-independent diffusion models were compared, with regions well-described by the former hypothesized to reflect cellular tissue, and those well-described by the latter expected to reflect necrosis or oedema. Technical and biological validation of the percentage of tissue described by the restricted diffusion microstructural model (termed %MM) was performed through simulations and histological comparison.

resultsSpatial and radiotherapy-related variation in model suitability was observed. %MM decreased from a mean of 64% at baseline to 44% 6 days post-radiotherapy in the treated group. %MM correlated negatively with the percentage of necrosis from histology, but overestimated it due to noise. Within MM regions, microstructural parameters were sensitive to radiotherapy-induced changes.

conclusionsThere is spatial and radiotherapy-related variation in different models' suitability for describing diffusion in tumor tissue, suggesting the presence of different and changing tumor sub-regions. The biological and technical validation of the proposed %MM cancer imaging biomarker suggests it correlates with, but overestimates, the percentage of necrosis.

Indexed as

Diffusion Magnetic Resonance ImagingNeoplasmsDiffusionHumansMagnetic Resonance ImagingTumor Microenvironmentdiffusion-weighted MRImicrostructural modelmodel selectionnecrosisradiotherapytumor microstructure

Identifiers

PMID32057115
PMCPMC7317874
OpenAlexW3006591678

What OpenQuestion holds

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LicenceCC BY
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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.