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Proteomic Signature in Breast Cancer: Correlation With Tumor Response to Neo-adjuvant Chemotherapy

Analysis of the Proteomic Signature in Breast Cancer Correlated With Tumor Response in Patients Necessitating a Neo-adjuvant Chemotherapy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00911911
Acronym
SPAM
Enrollment
66
Registered
2009-06-03
Start date
2007-02-22
Completion date
2012-01-16
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast cancer, Neo-adjuvant chemotherapy, Proteomic, Histological response

Brief summary

The scope of the trial is to identify proteomic signatures correlated with tumor response to neo-adjuvant chemotherapy.

Interventions

PROCEDUREBlood sampling

Taken at different times : inclusion, at the cycle 4 and at the cycle 6 during the neoadjuvant chemotherapy

PROCEDUREBIOPSY

Biopsy at the moment of inclusion, before neoadjuvant chemotherapy

PROCEDURESURGERY

Surgery after neoadjuvant chemotherapy

Sponsors

Centre Oscar Lambret
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women aged more than 18 years * Histologically proven breast carcinoma * Neo-adjuvant chemotherapy with anthracyclines and/or taxanes * No prior chemotherapy * Written informed consent

Exclusion criteria

* Metastatic disease

Design outcomes

Primary

MeasureTime frame
Proteomic analysis by SELDI-TOF on the tumor biopsy and blood samples Histological response according To Chevallier and Sataloff6 months

Secondary

MeasureTime frame
Correlation with node invasion6 months
Correlation with basal, luminal phenotypes, HER2 status or hormonal status6 months
Correlation with the response measured by ultrasound after chemotherapyAfter 3 and 5 months

Countries

France

Contacts

PRINCIPAL_INVESTIGATORBONNETERRE Jacques, MD, PhD

Centre Oscar Lambret

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026