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Breast Cancer (AKT Pathway Gene Testing) [Tissue]

Product Code: 02-BRCA-AKT-26

From £299.00 Early Bird

Early Bird Deadline: 31/01/2026

Deadline to order: 28/02/2026

PIK3CA, AKT1 and PTEN gene testing in breast cancer (FFPE)

Target/Genes:

Variants in the PIK3CA, AKT1 and PTEN genes.

Technology:

CNV, NGS, Panel testing, PCR based

Language:

English, French, German, Italian, Spanish

Sample Type:

FFPE

Accredited:

Yes

Sample Dispatch Date:

June 2026

Survey Period:

June - August 2026

Final Results:

December 2026 - January 2027

You can complete purchase on our secure partner site.

EQA Assessment

The scheme is designed to assess the analytical process (genotyping), and reporting (biological and clinical interpretation of the test result) including the overall report layout, content and clerical accuracy.

Sample Details

Three mock clinical cases with matching human tumour tissue paraffin embedded (FFPE) and/or artificial FFPE (designed to simulate real patient samples). One 10um or 15um FFPE section per case is provided.

Samples are provided as cut sections (rolled scrolls / curls) only – we cannot provide slide mounted materials. Variant allele frequencies of any artificial FFPE reference materials have been validated using ddPCR. 

EQA Results

Participants will receive an individual report including educational advice and a scheme report which includes additional information from the cohort of participants including geographical spread, methodologies employed, common errors, learning points and scheme statistics allowing participants to benchmark their results.

Each laboratory will also receive a single certificate listing all EQAs participated in with performance result for each year.

Participation Information

The minimum requirement is PIK3CA gene testing. If you provide a clinical service for the AKT1 and PTEN genes, these should be included.

These samples are not suitable for an RNA-based methodology only.

Participants are expected to test the samples according to their routine strategy. For all cases, participants are expected to return a clinical report and complete an online data collection form. 

This EQA is supported by an educational grant from AstraZeneca, fees are subsidised so there is a reduced cost for participants. EMQN would like to acknowledge and thank AstraZeneca for this support. 

Restricted to 150 participants, please register early to avoid disappointment. Open to laboratories from ALL countries (note: some restrictions may apply due to sanctions, delivery network exceptions, restrictions on importation etc)

 

How it works

Register

  • Enrol before the closing date
  • EMQN ships EQA samples or digital cases

Test & submit results

  • Analyse samples in your routine workflow
  • Upload results via your website account

Review & get certified

  • EMQN assesses your data
  • Receive your individual results, EQA summary report & certificate of participation

Enquire about this scheme

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