ForeSENTIA Tumour Profile

Synonyms: -
Material
Material:
FFPE tissue sample from a biopsy
Untersuchungsdauer
TAT:
2-3 weeks
Contact
Methode
Method:
NGS
Overview

ForeSENTIA is a tumour profiling test for solid tumours that provides clinically relevant information to support treatment decision-making. It evaluates a range of genomic alterations and key biomarkers associated with targeted therapies and immunotherapies, enabling a more individualised approach to patient management.

The test is designed for patients who require additional guidance on therapeutic options, particularly in cases where standard treatments are limited, ineffective, or no longer provide benefit. By identifying molecular features of the tumour, ForeSENTIA helps inform the selection of therapies that are more likely to be effective for a specific patient.

The test provides clinically actionable insights by evaluating important biomarkers such as microsatellite instability (MSI) and tumour mutational burden (TMB), alongside genetic alterations – single nucleotide variants (SNVs), small insertions & deletions (INDELs), copy number alternations (CNVs), selected rearrangements, linked to available therapies and ongoing clinical trials. This allows healthcare providers to expand treatment possibilities and consider options tailored specifically to the patient’s tumour profile.

ForeSENTIA offers a flexible panel structure to address different clinical needs:

  • 3 Pan-Cancer Tumour Profile panels, providing broad genomic coverage across multiple tumor types
  • 6 Cancer-Specific panels, focused on genes relevant to particular cancer types
  • 5 Gene-Focused panels, targeting key clinically actionable genes

A key advantage of ForeSENTIA is the integration of multiple clinically relevant analyses within a single test. In addition to identifying tumour-specific molecular characteristics, the report provides guidance on available treatment options and ongoing clinical trials, supporting a more precise and evidence-based approach to cancer care.

*ForeSENTIA does not diagnose cancer and is not a screening test. It cannot determine germline status. Possible hereditary implications require separate germline testing.

ForeSENTIA genetic tests

ForeSENTIA includes tumour genomic profiling panels designed to identify clinically actionable alterations across multiple cancer types. Selected panels evaluate genomic biomarkers relevant for immunotherapy such as tumour mutational burden (TMB) and microsatellite instability (MSI).

ForeSENTIA panels include:

  • 3 Comprehensive tumour profile panels: Pan-Cancer Advanced, Pan-Cancer Plus and Pan-Cancer Core
  • 6 Cancer-specific tumour profile panels: Breast/Gynecological, Colorectal, Glioma, Lung (NSCLC), Prostate, Melanoma
  • 5 Gene-focused tumour profile panels: BRAF, EGFR, IDH1 & IDH2, KRAS & NRAS, PIK3CA & AKT
  • testing of immunotherapy biomarkers MSI and TMB

Panel size varies depending on the selected test and may include extended gene coverage for comprehensive tumour profiling.

Benefits

COMPREHENSIVE

Charts the mutational landscape of tumours

EXTENSIVE

Tests for MSI and TMB

INFORMATIVE

Provides tailored therapy options

VALUABLE

Identifies eligible clinical trials

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.

Download materials

Physician flyer
Order form
Pan-Cancer Advanced genes and genetic alternations tested
Pan-Cancer Core cancer-specific genes and genetic alternations tested
Pan-Cancer Plus genes and genetic alternations tested
Transportation kit instructions

How to order a genetic test

Select the right test for your patients. Contact our team in case you do not have an active contract yet.
Collect the sample. Download and fill in the order and consent form or access our portal (available for sample sent to Germany).
Properly pack the sample and send it to Medicover Genetics.
The sample will be analysed in our accredited laboratories.
An actionable report will be available for you to access safely and securely.

Get in touch with us

Our team of experts is here to support you at every stage.

Please select the option that best describes you.
Please enter your first name.
Please enter your last name.
Providing your phone number is optional and helps us contact you more quickly if needed.
Please enter a valid email address
Please provide your country of residence. This information is required to route your request to the appropriate sales representative based on your location​.
Please enter your organisation / institution
Please do not enter sensitive health data or special categories of personal data here. If you need to share such information, please use a secure, separate communication channel, such as encrypted email, a protected patient portal or a confidential phone call.​

Your data will be used solely for processing your inquiry. For more information on how we handle your personal data and your rights, please refer to our .

Are you a patient?

Why Medicover Genetics

Leader in genetic testing with >25 years of experience in counselling and diagnostics

Comprehensive CE-IVD kit portfolio and seamless Technology Transfer solution for laboratories of any size

End-to-end clinical workflow from sample processing to sequencing analysis and reporting

CAP- accredited, GMP- and ISO9001, 15189 and 13485 certified

Certified laboratories