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Review
. 2024 Sep 29;7(1):261.
doi: 10.1038/s41746-024-01262-x.

Blending space and time to talk about cancer in extended reality

Affiliations
Review

Blending space and time to talk about cancer in extended reality

Tamsin J Robb et al. NPJ Digit Med. .

Abstract

We introduce a proof-of-concept extended reality (XR) environment for discussing cancer, presenting genomic information from multiple tumour sites in the context of 3D tumour models generated from CT scans. This tool enhances multidisciplinary discussions. Clinicians and cancer researchers explored its use in oncology, sharing perspectives on XR's potential for use in molecular tumour boards, clinician-patient communication, and education. XR serves as a universal language, fostering collaborative decision-making in oncology.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Integrating genomic, radiology and therapeutic cancer data in extended reality—a level playing field for enhanced multidisciplinary communication.
a Overview of the information displayed in the model, including interactive phylogenetic tree (left), central body model showing tumours (red) overlaid on organs (blue), with genomic data sites labelled and coloured according to shared genomic information in the phylogenetic tree, and interactive annotated timeline (right). b See tumours changing through time, with respect to other clinical information. Users may slide through a timeline, annotated with therapeutic information, to access radiology-based tumour information displayed on the main body model (in red, shown behind participants). c Recognise genomic tumour heterogeneity. The lung has been isolated from the main body model for detailed inspection. Sampled tumour sites for which genomic data was generated are annotated. Labels relate to sample site codes, with colouring representing the genomic clades of tumour-relatedness. d Workspace for multidisciplinary collaboration. The tool was designed to be used by up to ten participants simultaneously, allowing multidisciplinary teams to discuss different facets of the data and integrate their personal understanding of the layers of data together. For example, major tumours can be ‘pulled’ out of the main skeletal model, as can be seen here, where the participants on the left are examining the pancreatic tumour while the participants on the right are examining the primary lung tumour. A further participant is discerning extra information about tumour genomic data on a large monitor at the back of the room. A phylogenetic tree based on DNA variants shown to the left of the main patient model allows users to view the spatial distribution of tumours that share common genomic changes and indicate relatedness. Users may highlight a clade on the phylogenetic tree and observe these samples highlighted on the main model. Many tasks can be completed simultaneously by small groups of people, or alternatively, one user may guide all other participants through the dataset, with all users seeing the same information through their headsets. bd shows the view through one participant’s headset, while they are interacting with other participants.
Fig. 2
Fig. 2. Digital and physical elements come together to enable interdisciplinary discussions.
a Digital information accessible via Microsoft HoloLens MR headset, including patient model (within yellow circle at centre), model controls including time-slider and evolutionary tree (pink circle), and static overview graphics on the wall (green circle). b Physical elements enable best use of the model, including space to use traditional tools such as laptops and whiteboards, and ample space for members of the team to explore the data individually or together.

References

    1. Sharp, P. A. & Langer, R. Promoting convergence in biomedical science. Science333, 527–527 (2011). - PubMed
    1. Rolfo, C. et al. Multidisciplinary molecular tumour board: a tool to improve clinical practice and selection accrual for clinical trials in patients with cancer. ESMO Open3, e000398 (2018). - PMC - PubMed
    1. Moore, D. A. et al. Prospective analysis of 895 patients on a UK Genomics Review Board. ESMO Open4, e000469 (2019). - PMC - PubMed
    1. Dillekås, H., Rogers, M. S. & Straume, O. Are 90% of deaths from cancer caused by metastases? Cancer Med8, 5574–5576 (2019). - PMC - PubMed
    1. Perakis, S. O. et al. Comparison of three commercial decision support platforms for matching of next-generation sequencing results with therapies in patients with cancer. ESMO Open5, e000872 (2020). - PMC - PubMed

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