Urine-derived bladder cancer organoids (urinoids) as a tool for cancer longitudinal response monitoring and therapy adaptation

Publication date

2024-02-24

Authors

Viergever, Bas
Raats, Daniëlle A E
Geurts, Veerle
Mullenders, Jasper
Jonges, Trudy G.N.ISNI 0000000389945256
van der Heijden, Michiel S
van Es, Johan H.
Kranenburg, Onno
Meijer, Richard PORCID 0000-0003-2510-7982

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Advisors

Supervisors

Document Type

Article

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cc_by

Abstract

BACKGROUND: Bladder cancer is one of the most common cancer types worldwide. Generally, research relies on invasive sampling strategies. METHODS: Here, we generate bladder cancer organoids directly from urine (urinoids). In this project, we establish 12 urinoid lines from 22 patients with non-muscle and muscle-invasive bladder tumours, with an efficiency of 55%. RESULTS: The histopathological features of the urinoids accurately resemble those of the original bladder tumours. Genetically, there is a high concordance of single nucleotide polymorphisms (92.56%) and insertions & deletions (91.54%) between urinoids and original tumours from patient 4. Furthermore, these urinoids show sensitivity to bladder cancer drugs, similar to their tissue-derived organoid counterparts. Genetic analysis of longitudinally generated tumoroids and urinoids from one patient receiving systemic immunotherapy, identify alterations that may guide the choice for second-line therapy. Successful treatment adaptation was subsequently demonstrated in the urinoid setting. CONCLUSION: Therefore, urinoids can advance precision medicine in bladder cancer as a non-invasive platform for tumour pathogenesis, longitudinal drug-response monitoring, and therapy adaptation.

Keywords

Oncology, Cancer Research, Journal Article

Citation

Viergever, B J, Raats, D A E, Geurts, V, Mullenders, J, Jonges, T N, van der Heijden, M S, van Es, J H, Kranenburg, O & Meijer, R P 2024, 'Urine-derived bladder cancer organoids (urinoids) as a tool for cancer longitudinal response monitoring and therapy adaptation', British Journal of Cancer, vol. 130, no. 3, pp. 369-379. https://doi.org/10.1038/s41416-023-02494-6