Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06706570

PIK3CA Mutational Status Assessment

Evaluation of PIK3CA mutational status: a route towards a tailored diagnostic approach.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

European Institute of Oncology

Milan, MI, 20141, Italy

Location status: Recruiting

Location contact

Nicola Fusco, MD

CONTACT

[email protected]

00390294372079

About this study

Evaluate the effectiveness and concordance of molecular methods in identifying mutations affecting the PIK3CA gene both on paraffin tissue sections of the tumor and on liquid biopsy of patients with breast cancer treated at the IEO. The molecular test on the liquid biopsy of same patient could bring an important benefit considering that the withdrawal of this biomaterial turns out to be less invasive than a biopsy performed on an organ

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant has a histologically and/or cytologically confirmed diagnosis of ER+ and/or PgR+ breast cancer by local laboratory.
  • Participant has HER2-negative breast cancer defined as a negative in situ hybridization test or an IHC status of 0, 1+ or 2+. If IHC is 2+, a negative in situ hybridization (Fluorescent in situ hybridization (FISH), Chromogenic in situ hybridization (CISH), or Silver-enhanced in situ hybridization (SISH)) test is required by local laboratory testing.
  • Participants should be at advanced or metastatic setting prior to treatment.
  • Written informed consent must be signed and dated by the patient and the investigator prior to inclusion.
  • Patients must be accessible for follow-up.

Exclusion criteria

  • patients already treated with different treatments like chemotherapy, hormone therapy etc

Treatment and study plan

Primary outcomes

  1. Evaluation of PIK3CA mutational status: a path towards a "tailored" diagnostic approach.

    Time frame: 2 years

    Investigate concordance between sequencing panels again generation (NGS) based on different principles and different RT-PCR assays in detecting mutations of PIK3CA.

Study contacts

Contact information is provided by the study sponsor or research team.

Nicola Fusco, MD

CONTACT

[email protected]

00390294372079

francesca lombardi, biologist

CONTACT

[email protected]

00390257489425

Sponsors and collaborators

Lead sponsor

European Institute of Oncology

Other

Registry information

Official study title

PIK3CA Mutational Status Assessment: Towards a "Tailored" Diagnostic Approach

Important dates

Study start
2024
Primary completion
2026
Study completion
2030
First posted
Nov 26, 2024
Registry last updated
Mar 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.