Actively Recruiting

Age: 18Years +
FEMALE
NCT04504747

Real Time Molecular Analysis of Breast Cancer Receiving Neo-adjuvant Chemotherapy

Led by Institut Paoli-Calmettes · Updated on 2025-06-15

150

Participants Needed

1

Research Sites

373 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present project aims at identifying robust candidates for drug resistance in BC patients eligible for NAC. Its originality lies upon the combination of three different and complementary prospective approaches: from the molecular analyses of biopsies sampled before and after NAC, from in vitro BC Patient-Derived Organoids (PDO) mimicking patient's response to NAC, and from Circulating Tumor Cells (CTCs) isolated before/during/after NAC.

CONDITIONS

Official Title

Real Time Molecular Analysis of Breast Cancer Receiving Neo-adjuvant Chemotherapy

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Woman over 18
  • Signed consent to participate
  • Histologically or cytologically confirmed invasive mammary adenocarcinoma
  • Indication for neo-adjuvant chemotherapy by clinical team
  • No contraindication to neo-adjuvant chemotherapy
  • Planned surgery and radiotherapy after neo-adjuvant chemotherapy
  • Performance status of 0 or 1 (WHO scale)
  • Affiliated with or beneficiary of a social security scheme
Not Eligible

You will not qualify if you...

  • Planned treatment including neo-adjuvant radiotherapy before surgery
  • Metastatic breast cancer at diagnosis
  • Previous breast cancer relapse
  • Other cancer within the past 3 years except treated low-risk cancers
  • Pregnant, likely to be pregnant without effective contraception, or breastfeeding
  • Under legal protection or unable to give consent
  • Unable to attend medical follow-up due to geographical, social, or psychological reasons

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institut Paoli-Calmettes

Marseille, Marseille, France, 13009

Actively Recruiting

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Research Team

J

j PAKRADOUNI, PharmD,PhD

CONTACT

L

Laurie-Anne GOUTY, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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