Prostate Cancer
Prostate cancer accounted for approximately 1.55 million new cases worldwide in 2024, representing 7.5% of all newly diagnosed cancers and making it the fourth most commonly diagnosed cancer globally. The WHO Classification describes the morphological and molecular features of prostatic tumours, while clinical guidelines address the use of molecular testing for prognosis and treatment selection. In routine practice, the diagnosis and classification of most prostate carcinomas remain primarily histomorphological. Molecular and biomarker testing has its greatest established clinical relevance in advanced disease, where it can identify alterations associated with targeted or tumour-agnostic treatment options.
Available tests
The sequencing and the fusion gene analysis listed below can be ordered individually or together as one combined analysis.
This analysis focuses on selected treatment-relevant genes and does not constitute comprehensive genomic profiling. Depending on the clinical setting, additional testing may be indicated, including analysis of CDK12, assessment of PTEN expression, tumour mutational burden (TMB), MMR protein expression, germline testing, or broader DNA/RNA profiling.
Single-method analysis | Panel | Gene scope | Purpose |
| Sequencing | Panel00751 | ATM, BRAF, BRCA1, BRCA2, CHEK2, FANCA, PALB2, RAD51D | Detection of sequence variants in tumour tissue |
| Fusion gene analysis | Panel00749 | NTRK1, NTRK2, NTRK3 | Detection of gene fusions in tumour tissue |
| Microsatellite instability (MSI) | Panel00750 | Microsatellite marker analysis | Determination of tumour MSI status |
Combined analysis | Panel | Gene scope |
| Combined focused analysis | Panel00541 | ATM, BRAF, BRCA1, BRCA2, CHEK2, FANCA, PALB2, RAD51D, NTRK1, NTRK2, NTRK3 |
Additional tumour analyses, including TMB assessment and an assay-specific HRD or genomic-instability assessment, are available as part of Panel00617 ().
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