Molecular Profiling in Young (<50 Years of Age) Patients With Metastatic Breast Cancer
Primary Purpose
Breast Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
FoundationOne CDx
Sponsored by
About this trial
This is an interventional diagnostic trial for Breast Cancer focused on measuring Young patient, Asian
Eligibility Criteria
Inclusion Criteria:
- Patients between 19 - 50 years of age on the day of signing informed consent.
- Able to provide written informed consent for voluntary participation in the trial.
- With metastatic breast cancer
- Willing to provide biopsies from the primary tumor or lymph nodes at screening to the central laboratory. (with at least 10 unstained slides and 1 H&E slide)
Exclusion Criteria:
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the study.
Sites / Locations
- Seoul National University Hospital
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
FMI
Arm Description
FoundationOne CDx will be performed using archival tumor tissue
Outcomes
Primary Outcome Measures
Genetic characteristic of young (<50 years of age) Korean patients with metastatic breast cancer.
Genetic characteristics will be evaluated using FoundationOne CDx.
Secondary Outcome Measures
Evaluate the prognostic and predictive role of tumor mutation burden
Tumor mutation burden will be analysed using FoundationOne CDx.
Reveal the correlation between genetic characteristics and immunohistochemical expression of selected proteins.
FoundationOne CDx results and immunohistochemical expression will be analysed.
Compare molecular characteristics of breast cancer according to age groups.
Genetic characteristics will be analysed according to age groups.
To offer genomic profiling guided therapy to patients To explore how genomic profiling guided therapy could improve patient outcome as an ad-hoc if sufficient number of patients can be followed up (compared to historic data).
The result of FoundationOne CDx will be used in patient treatment
Full Information
NCT ID
NCT04098640
First Posted
September 19, 2019
Last Updated
September 19, 2019
Sponsor
Seoul National University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04098640
Brief Title
Molecular Profiling in Young (<50 Years of Age) Patients With Metastatic Breast Cancer
Official Title
Molecular Profiling Using FoundationOne CDx in Young (<50 Years of Age) Patients With Metastatic Breast Cancer (ML41263)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 2019 (Anticipated)
Primary Completion Date
July 2021 (Anticipated)
Study Completion Date
July 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Breast cancer is the most common cancer in women worldwide, especially in developed countries. In developing countries, including South Korea, the incidence and mortality rate of breast cancer is rapidly increasing. One of the most important characteristics of breast cancer in South Korea, as well as in other Asian countries, is the younger onset of disease compared to Western.
Medical treatment of breast cancer is evolving rapidly, incorporating immune checkpoint blockades and molecularly targeted agents. However, data and knowledge are still limited in terms of molecular characteristics of Asian breast cancer, compared to that of Western countries, and this remains a major hurdle for drug development in Asian breast cancer patients.
The primary objective of this study is to elucidate the genetic characteristic of young (<50 years of age) Korean patients with metastatic breast cancer using FoundationOne CDx.
Detailed Description
Secondary Objective(s):
To evaluate the prognostic and predictive role of tumor mutation burden.
To reveal the correlation between genetic characteristics and immunohistochemical expression of selected proteins (including DNA damage repair (DDR) molecules and various immune modulating molecules including PD-L1, PD-1, IDO, and OX40).
Compare molecular characteristics of breast cancer according to age groups (<35 years vs. 35-50 years).
To offer genomic profiling guided therapy to patients as early as possible (preferably, 1st- or 2nd-line of treatment). In addition, to explore how genomic profiling guided therapy could improve patient outcome as an ad-hoc if sufficient number of patients can be followed up (compared to historic data).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Young patient, Asian
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
FMI
Arm Type
Other
Arm Description
FoundationOne CDx will be performed using archival tumor tissue
Intervention Type
Genetic
Intervention Name(s)
FoundationOne CDx
Intervention Description
FoundationOne CDx will be performed using archival tumor tissue
Primary Outcome Measure Information:
Title
Genetic characteristic of young (<50 years of age) Korean patients with metastatic breast cancer.
Description
Genetic characteristics will be evaluated using FoundationOne CDx.
Time Frame
After the end of patient enrollment
Secondary Outcome Measure Information:
Title
Evaluate the prognostic and predictive role of tumor mutation burden
Description
Tumor mutation burden will be analysed using FoundationOne CDx.
Time Frame
After the end of patient enrollment
Title
Reveal the correlation between genetic characteristics and immunohistochemical expression of selected proteins.
Description
FoundationOne CDx results and immunohistochemical expression will be analysed.
Time Frame
After the end of patient enrollment
Title
Compare molecular characteristics of breast cancer according to age groups.
Description
Genetic characteristics will be analysed according to age groups.
Time Frame
After the end of patient enrollment
Title
To offer genomic profiling guided therapy to patients To explore how genomic profiling guided therapy could improve patient outcome as an ad-hoc if sufficient number of patients can be followed up (compared to historic data).
Description
The result of FoundationOne CDx will be used in patient treatment
Time Frame
After the end of patient enrollment
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients between 19 - 50 years of age on the day of signing informed consent.
Able to provide written informed consent for voluntary participation in the trial.
With metastatic breast cancer
Willing to provide biopsies from the primary tumor or lymph nodes at screening to the central laboratory. (with at least 10 unstained slides and 1 H&E slide)
Exclusion Criteria:
Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seock-Ah Im, MD PhD
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
110-744
Country
Korea, Republic of
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Molecular Profiling in Young (<50 Years of Age) Patients With Metastatic Breast Cancer
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