Prostate Cancer

Synonyms: -
Material
Material:
FFPE tissue sections
Untersuchungsdauer
TAT:
varies depending on the analysis
Contact
Methode
Method:
NGS
Overview

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, NTRK3Detection 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 analysisPanel00541ATM, 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 ().

Created by

Our editorial team consists of medical specialists and scientists in the field of human genetics. All content is created and reviewed in accordance with current scientific standards.

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