Paper detail

Benchmarking features from different radiomics toolkits / toolboxes using Image Biomarkers Standardization Initiative

There is no consensus regarding the radiomic feature terminology, the underlying mathematics, or their implementation. This creates a scenario where features extracted using different toolboxes could not be used to build or validate the same model leading to a non-generalization of radiomic results. In this study, the image biomarker standardization initiative (IBSI) established phantom and benchmark values were used to compare the variation of the radiomic features while using 6 publicly available software programs and 1 in-house radiomics pipeline. All IBSI-standardized features (11 classes, 173 in total) were extracted. The relative differences between the extracted feature values from the different software and the IBSI benchmark values were calculated to measure the inter-software agreement. To better understand the variations, features are further grouped into 3 categories according to their properties: 1) morphology, 2) statistic/histogram and 3)texture features. While a good agreement was observed for a majority of radiomics features across the various programs, relatively poor agreement was observed for morphology features. Significant differences were also found in programs that use different gray level discretization approaches. Since these programs do not include all IBSI features, the level of quantitative assessment for each category was analyzed using Venn and the UpSet diagrams and also quantified using two ad hoc metrics. Morphology features earns lowest scores for both metrics, indicating that morphological features are not consistently evaluated among software programs. We conclude that radiomic features calculated using different software programs may not be identical and reliable. Further studies are needed to standardize the workflow of radiomic feature extraction.

preprint2020arXivOpen access
0citations
0reviews
0saves
Nocode
Nodataset
0institutions

Next steps

Decide what to do with this paper

Use like or dislike for the fast social read. The more specific scholarly feedback stays available below when needed.

Log in to curate

Reading frame

Keep the important context close to the paper

Keep the important signals around this paper in one place: votes, save state, collection context, reviews and the metadata you need before deciding what to do next.

Institutions

Add specific reaction

Move through the context

Research map

Open full explorer

Move through nearby people, institutions, topics and adjacent work without leaving the paper page.

Building this graph slice

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Structured reviews

0 review(s)

ContributeLeave structured feedbackUse the review template when you have a concrete strength, concern or method question.Open review form

No structured reviews yet. High-signal critique starts here.

Work discussion

0 comment(s)

DiscussAdd a high-signal commentKeep quick notes, caveats and replication pointers separate from formal reviews.Open comment form

No discussion yet. The first strong comment sets the tone.