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Lesion segmentation protocol #9

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This PR adds the lesion segmentation protocol which was first discussed in issue 77 from the CanProCo repo.

The lesion segmentation protocol adds an .md file at the base of this repository.

Feedback and improvements are welcomed !

@plbenveniste plbenveniste added the documentation Improvements or additions to documentation label Mar 21, 2024
@plbenveniste plbenveniste self-assigned this Mar 21, 2024
@jcohenadad jcohenadad requested a review from maxradx April 10, 2024 13:55
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This is a great start @plbenveniste ! Thank you for initiating this. I would add a few visual examples of lesion segmentation, so we can all agree on how 'conservative' we want to be with our segmentations. Maybe that could be reserved to an 'example' section.

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The following details the protocol for Multiple Sclerosis (MS) lesion segmentation in the spinal cord.
Imaging the spinal cord is often essential to confirm the diagnosis of MS. That is because the lesions of the spinal cord are included in the McDonald diagnosis criteria, which studies dissemination in space and in time [(Thompson et al. 2018)](https://pubmed.ncbi.nlm.nih.gov/29275977/). While the MAGNIMS-CMSC-NAIMS working group recommends to use at least two sagittal images for MS diagnosis, still, axial imaging is mentioned as optional in international imaging guidelines [(Wattjes et al. 2021)](https://pubmed.ncbi.nlm.nih.gov/34139157/).
For detecting MS lesions in the spinal cord, two main contrasts emerge: PSIR and STIR contrasts. New studies [(Peters et al. 2024)](https://pubmed.ncbi.nlm.nih.gov/38289376/)[(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that using PSIR contrasts improved MS lesion detection in the spinal cord. [(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that the PSIR contrast showed a higher signal-to-noise (SNR) ratio compared to the STIR contrast.
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Maybe my suggestion is not up-to-date, but I have doubts/questions abouts STIR sequences being frequently used for assessing MS lesions, at least in standard/basics protocols (even if mentioned in the picture showing example of of clinically used sequences for MS). From my understanding, the most useful sequence for detecting MS lesions in clinical practice is proton density (PD), but probably that changes from sites/radiologists perspective.
basic_sequences
According to the articles, PSIR sequences seem great! However, here are some potential precisions I would address :
1-Peters and al : PSIR compared to STIR (not the best...) and T2;
2-Fechner : PSIR compared to T2 and T1C+ sequences (not compared to PD sequences...)

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For detecting MS lesions in the spinal cord, two main contrasts emerge: PSIR and STIR contrasts. New studies [(Peters et al. 2024)](https://pubmed.ncbi.nlm.nih.gov/38289376/)[(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that using PSIR contrasts improved MS lesion detection in the spinal cord. [(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that the PSIR contrast showed a higher signal-to-noise (SNR) ratio compared to the STIR contrast.
For detecting MS lesions in the spinal cord, two main contrasts emerge: PSIR and STIR contrasts. New studies [(Peters et al. 2024)](https://pubmed.ncbi.nlm.nih.gov/38289376/)[(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that using PSIR contrasts improved MS lesion detection in the spinal cord. [(Fechner et al. 2019)](https://pubmed.ncbi.nlm.nih.gov/30679225/) showed that the PSIR contrast showed a higher signal-to-noise (SNR) ratio compared to the STIR contrast.


## Criteria to segment MS lesions in the spinal cord:

Do not segment lesions in images with too many artifacts (such as this one : https://github.com/ivadomed/canproco/issues/53#issue-1938136790). Preferably, add the image to the exclude file so that it isn’t used for model training…
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Question : in words, what would be an image considered being too artefacted? Any criteria?

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Do not segment lesions in images with too many artifacts (such as this one : https://github.com/ivadomed/canproco/issues/53#issue-1938136790). Preferably, add the image to the exclude file so that it isn’t used for model training…
Do not segment lesions in images with too many artifacts (such as this one : https://github.com/ivadomed/canproco/issues/53#issue-1938136790). Preferably, add the image to the exclude file so that it isn’t used for model training…

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i would also reference related initiatives-- eg

there are other important initiatives

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Co-authored-by: Julien Cohen-Adad <[email protected]>
plbenveniste and others added 8 commits April 11, 2024 11:39
Co-authored-by: Julien Cohen-Adad <[email protected]>
Co-authored-by: Julien Cohen-Adad <[email protected]>
Co-authored-by: Julien Cohen-Adad <[email protected]>
Co-authored-by: Julien Cohen-Adad <[email protected]>
Co-authored-by: Julien Cohen-Adad <[email protected]>
Co-authored-by: Julien Cohen-Adad <[email protected]>
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plbenveniste commented Apr 11, 2024

Look at MSSEG challenge's public data to find cases of MS lesions in the spinal cord. The objective is to build a dataset for lesion segmentation training.
Also look at the MSSEG challenge article to get inspiration from the segmentation protocol

Furthermore, it is recommended to get familiar with SCT for creating QCs and for manual correction ([SCT tutorial](https://spinalcordtoolbox.com/user_section/tutorials.html)).

## Step 2: Spinal cord anatomy and lesion segmentation
Before, moving on to MS lesion segmentation, trainees are advised to study the neuroanatomical structures of healthy spinal cords. Trainees should look at healthy spinal cords in MRI images of different contrasts: T2w, T1w, PSIR, STIR, MP2RAGE... A public dataset will be built for this purpose.
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SpineGeneric could be used for this purpose

## Step 2: Spinal cord anatomy and lesion segmentation
Before, moving on to MS lesion segmentation, trainees are advised to study the neuroanatomical structures of healthy spinal cords. Trainees should look at healthy spinal cords in MRI images of different contrasts: T2w, T1w, PSIR, STIR, MP2RAGE... A public dataset will be built for this purpose.

To learn the specificity of MS lesions, trainees should work on differentiating MS lesions from other diseases.
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Which disease should be used ? NMO ?

We should also look into building this public dataset: which public data do we have ?


To learn the specificity of MS lesions, trainees should work on differentiating MS lesions from other diseases.

One of the most challenging task of MS lesion segmentation is to distinguish the border of a lesion and the cerebrospinal fluid (CSF). To learn where to draw the lesion border, a set of tricky examples validated by a NeuroRadioligist will be created.
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Which data should be used? MSSEG data? Ask a collaborator to help us on this?


To learn the specificity of MS lesions, trainees should work on differentiating MS lesions from other diseases.

One of the most challenging tasks of MS lesion segmentation is to distinguish the border of a lesion and the cerebrospinal fluid (CSF). To learn where to draw the lesion border, a set of tricky examples validated by a NeuroRadioligist will be created.
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Reference the videos made by Julien during work with Michelle Chen regarding MS lesion segmentation

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Referencing this lesion atlas which could be very useful in creating this lesion seg protocol: https://link.springer.com/book/10.1007/978-3-540-71372-2

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