IDENTITY: InheriteD brEast caNcer iTalian regIsTrY A Retrospective-prospective Observational Cohort Study to Evaluate Cancer Prevention Strategies in Women With a Deleterious Mutation in BRCA1-2

Sponsor
Centro di Riferimento Oncologico - Aviano (Other)
Overall Status
Recruiting
CT.gov ID
NCT05835739
Collaborator
(none)
78
12
193.1
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Study Details

Study Description

Brief Summary

The purpose of the study is to obtain and centralize data about cancer prevention strategies in women with a germline deleterious mutation in BRCA1-2 with or without a history of breast cancer in Italy

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Women who carry a deleterious mutation in breast cancer susceptibility gene 1 (BRCA1) or breast cancer susceptibility gene 2 (BRCA2) have an elevated lifetime risk of developing breast and ovarian cancer, estimated at up to 7 and 25 times that of the average risk population, respectively. By the age of 80 years, the estimated cumulative risk of breast cancer is about 70% for BRCA1/2 mutation carriers, while the cumulative ovarian cancer risk is about 40% for BRCA1 and 20% for BRCA2 carriers. Thus, BRCA1/2 mutation carriers are advised to consider different risk-reducing strategies, including surveillance (breast self-examination, clinical breast examination, screening using mammography, ultrasound and breast magnetic resonance imaging), chemoprevention and prophylactic surgery (prophylactic mastectomy and/or salpingo-oophorectomy). Prospective cohort studies demonstrate that risk-reducing mastectomy is associated with 90% or more decreased risk of breast cancer. Unfortunately, it is difficult to quantify its effect on overall mortality since no randomized studies have compared risk-reducing mastectomy with enhanced screening, risk-reducing salpingo oophorectomy or prophylactic treatment. Additionally, prophylactic mastectomy is an invasive intervention associated with a substantial complication rate and psychological distress, changes in body image and sexual function. Therefore, as a preventive measure, risk-reducing mastectomy should be discussed on a case-by case basis, after proper counseling regarding benefits, limitations, risks of surgical complications and psychosocial impact. Conversely, risk-reducing salpingo oophorectomy is strongly recommended for women with mutations in BRCA1 (between ages 35 and 40 years) and BRCA2 (between ages 40 and 45 years) after completion of childbearing desire, for a significant reduction in ovarian cancer incidence and all-cause mortality. In the absence of solid evidences coming from randomized clinical trials, the aim of the present study is to collect and centralize real-world data on cancer prevention strategies (prophylactic surgery, prophylactic therapies, active surveillance) and oncologic treatments of women with a deleterious mutation in BRCA1-2 with or without a diagnosis of breast cancer in Italy. By collecting and analyzing these data, the IDENTITY study aims to obtain a faithful representation of the practices related to oncological surveillance in the group of patients analyzed.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    78 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    InheriteD brEast caNcer iTalian regIsTrY A Retrospective-prospective Observational Cohort Study to Evaluate Cancer Prevention Strategies in Women With a Deleterious Mutation in BRCA1-2
    Actual Study Start Date :
    Aug 27, 2019
    Anticipated Primary Completion Date :
    Sep 30, 2025
    Anticipated Study Completion Date :
    Sep 30, 2035

    Arms and Interventions

    Arm Intervention/Treatment
    Cohort A (Retrospective)

    all consecutive women with a germline deleterious mutation in BRCA1-2 admitted to the participant Center since 1st of January 2010 until site activation will be enrolled

    Cohort B (Prospective):

    all consecutive women with a germline deleterious mutation in BRCA1-2 admitted to the participant Center since site activation until September 2025 will be enrolled

    Outcome Measures

    Primary Outcome Measures

    1. To obtain and centralize data about cancer prevention strategies in women with a germline deleterious mutation in BRCA1-2 with or without a history of breast cancer in Italy [10 years since enrolment]

      To obtain and centralize data about cancer prevention strategies in women with a germline deleterious mutation in BRCA1-2 with or without a history of breast cancer in Italy

    Secondary Outcome Measures

    1. To evaluate the clinico-radiological follow-up (type and frequency) of women with a germline deleterious mutation in BRCA1-2 with or without a history of early breast cancer [10 years since enrolment]

      To evaluate the clinico-radiological follow-up (type and frequency) of women with a germline deleterious mutation in BRCA1-2 with or without a history of early breast cancer

    2. To evaluate the treatment of early and/or advanced breast cancer in women with a germline deleterious mutation in BRCA1-2 [10 years since enrolment]

      To evaluate the treatment of early and/or advanced breast cancer in women with a germline deleterious mutation in BRCA1-2

    3. To evaluate disease-free survival and/or progression-free survival and overall survival of women with a germline deleterious mutation in BRCA1-2 treated for early and/or advanced breast cancer [10 years since enrolment]

      To evaluate disease-free survival and/or progression-free survival and overall survival of women with a germline deleterious mutation in BRCA1-2 treated for early and/or advanced breast cancer

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    Cohort A (Retrospective):
    1. Female sex

    2. Age ≥ 18 years

    3. Signed informed consent

    4. Documented germline deleterious mutation in BRCA1 and/or BRCA2 in people with: i) No history of cancer ii) Radically treated breast cancer iii) Stage IV breast cancer diagnosed after BRCA1-2 mutation detection

    5. Admission to the participating Center since 1st of January 2010, prior to site activation

    Cohort B (Prospective):
    1. Female sex

    2. Age ≥ 18 years

    3. Signed informed consent

    4. Documented germline deleterious mutation in BRCA1 and/or BRCA2 in people with: i) No history of cancer ii) Radically treated breast cancer iii) Stage IV breast cancer diagnosed after BRCA1-2 mutation detection

    5. Admission to the participating Center after site activation

    Exclusion Criteria:
    Cohort A/B (Retrospective/Prospective):
    1. Other malignancies diagnosed within five years prior to BRCA1-2 mutation detection, except for:
    • ovarian cancer stage I-II

    • basal or squamous cell carcinoma of the skin

    • melanoma in situ

    • CIS of the cervix

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centro di Riferimento Oncologico - Aviano Aviano Pordenone Italy 33081
    2 IRCCS AOU San Martino, IST Genova Genova Italy
    3 Azienda Ospedaliera Papardo Messina Italy
    4 ASST Ovest Milanese Milano Italy
    5 Azienda ospedaliera Universitaria di Modena Modena Italy
    6 Università degli studi di Napoli Federico II Napoli Italy
    7 Azienda AUSL IRCCS - Reggio Emilia Reggio Emilia Italy
    8 ASL Roma 1, Santo Spirito Roma Italy
    9 IFO - Istituto Regina Elena (Oncologia medica 2) Roma Italy
    10 Policlinico Universitario Gemelli Roma Italy
    11 Città della salute Torino, PO S. Anna Torino Italy
    12 ASU FC Azienda Sanitaria Universitaria Friuli Centrale Udine Italy

    Sponsors and Collaborators

    • Centro di Riferimento Oncologico - Aviano

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centro di Riferimento Oncologico - Aviano
    ClinicalTrials.gov Identifier:
    NCT05835739
    Other Study ID Numbers:
    • CRO-2019-33
    First Posted:
    Apr 28, 2023
    Last Update Posted:
    Apr 28, 2023
    Last Verified:
    Apr 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 28, 2023