Transcutaneous Breast Cancer Diagnosis by Canine Odorology

  • STATUS
    Recruiting
  • participants needed
    450
  • sponsor
    Institut Curie
Updated on 19 February 2024
insulin
corticosteroids
fever
breast carcinoma
carcinoma
cancer diagnosis
breast imaging reporting and data system
ultrasound breast

Summary

Patient with an indication of interventional percutaneous procedure for characterization of a breast lesion, palpable or not, classified as category 4 or 5, according to the Breast Imaging (BI) Report and Data System of the American College of Radiology (RADS) classification detected at mammography and/or breast ultrasound examination.

Details
Condition Breast Cancer, Breast Cancer
Age 18years - 100years
Treatment Odour sampling
Clinical Study IdentifierNCT04217109
SponsorInstitut Curie
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Women 18 years and older, with one or more ipsilateral mammary lesion(s), palpable or not, detected at mammography and/or ultrasound and with at least one lesion classified as BI-RADS category 4 or 5 with an indication of percutaneous sampling (cytology, microbiopsies, macro-biopsies)
Benefit from the national social security
Signature of the informed consent of the study
There is no contraindication for the person to simultaneously participate to another research program and there is no exclusion period planned after the study

Exclusion Criteria

Patient with bilateral breast lesions classified as BI-RADS category 4 or 5
Patient with breast implant(s)
Patient with a personal history of breast surgery for benign lesion(s) of the concerned breast operated less than 4 weeks before the date of inclusion in this study
Patient with a personal history of cancer (in situ or invasive) less than 5 years before inclusion whatever the anatomical site including cutaneous basal cell carcinoma
Patient with a personal history of punctures and/or percutaneous breast biopsies of the concerned breast less than 4 weeks before inclusion
Patient with a breast skin ulceration
Patient under insulin (risk of sudation that may impair compress sample)
Concomitant antibiotics or corticoids taken one week before inclusion in the study
Patient with a current viral infection (fever)
Persons under guardianship or deprived of liberty
Impossibility to submit to the medical monitoring expected by the study for geographical or severe psychological reasons
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