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Mutation of BRCA1/2 and Other Potential Genes in Triple-negative Breast Cancer

Primary Purpose

Breast Cancer

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Mutation analysis
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Breast Cancer focused on measuring BRCA1/2;Mutations;Neoadjuvant chemotherapy;TNBC

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients receiving neoadjuvant chemotherapy with paclitaxel and carboplation are enrolled in this study.

  • (1) histologically confirmed mainly invasive breast carcinoma
  • (2) a unilateral and non-inflammatory tumors
  • (3) status of ER, PR and HER-2 are available and negative
  • (4) The participants are required to have clinical stage II or III breast cancer with a clinical or radiographically measurable residual tumor after core biopsy.
  • (5)patients had pathological evaluation after NAC
  • (6) the pathologic tissues are available for immunohistochemistry and next generation sequencing

Exclusion Criteria:

  • (1) carcinoma in situ
  • (2) received less than 4 cycles neoadjuvant chemotherapy

Sites / Locations

  • Department of Breast Surgery, Cancer Hospital, Fudan University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Mutation analysis- NACwith PCR

Mutation analysis-NAC with SD/PD.

Arm Description

consisting of 50 patients undergoing NACwith pathological compete response

consisting of 50 patients undergoing NAC with SD/PD

Outcomes

Primary Outcome Measures

Gene mutation prevalence of tBRCA1/2, HRR, or other chemo-response related genes in TNBC patients between pCR and SD/PD, which achieved after NAC

Secondary Outcome Measures

To evaluate potential relationship between these gene mutations and NAC-response in TNBC patients

Full Information

First Posted
January 28, 2016
Last Updated
January 28, 2016
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT02670668
Brief Title
Mutation of BRCA1/2 and Other Potential Genes in Triple-negative Breast Cancer
Official Title
Single Centre,Exploratory,Parallel and Retrospective Study to Analysis the Mutation and Expression of BRCA1/2 and Other Potential Genes in Triple-negative Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is to determine the prevalence of potential chemo-response related genes mutation in TNBC patients between pCR and SD/PD group, which achieved after NAC; and to evaluate potential relationship between these gene mutations and NAC-response in TNBC patients.Based on the results,we can further characterize TNBC from a phenotypical and molecular perspective, in order to identify potential new target agents and to individualize the treatment.
Detailed Description
This is single centre,exploratory,parallel and retrospective study to analysis the mutation and expression of tBRCA1/2 and other potential genes in triple-negative breast cancer. Patients received neoadjuvant chemotherapy with paclitaxel and carboplation are enrolled in this study. The participants are required to have clinical stage II or III breast cancer with a clinical or radiographically measurable residual tumor after core biopsy. We will enroll the patients of pCR or SD/PD, which achieved after complete NAC. Every group will enroll 50 patients. This study is to identify relationship between different gene mutations and expression, which may be targeted with currently available investigational drugs, and chemo-response. Patients who will fulfil all inclusion/exclusion criteria. We conducted a retrospective chart review of the 100 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
BRCA1/2;Mutations;Neoadjuvant chemotherapy;TNBC

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mutation analysis- NACwith PCR
Arm Type
Experimental
Arm Description
consisting of 50 patients undergoing NACwith pathological compete response
Arm Title
Mutation analysis-NAC with SD/PD.
Arm Type
Experimental
Arm Description
consisting of 50 patients undergoing NAC with SD/PD
Intervention Type
Other
Intervention Name(s)
Mutation analysis
Primary Outcome Measure Information:
Title
Gene mutation prevalence of tBRCA1/2, HRR, or other chemo-response related genes in TNBC patients between pCR and SD/PD, which achieved after NAC
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
To evaluate potential relationship between these gene mutations and NAC-response in TNBC patients
Time Frame
Baseline

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients receiving neoadjuvant chemotherapy with paclitaxel and carboplation are enrolled in this study. (1) histologically confirmed mainly invasive breast carcinoma (2) a unilateral and non-inflammatory tumors (3) status of ER, PR and HER-2 are available and negative (4) The participants are required to have clinical stage II or III breast cancer with a clinical or radiographically measurable residual tumor after core biopsy. (5)patients had pathological evaluation after NAC (6) the pathologic tissues are available for immunohistochemistry and next generation sequencing Exclusion Criteria: (1) carcinoma in situ (2) received less than 4 cycles neoadjuvant chemotherapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ayong Cao, MD
Phone
+86 13917406138
Email
caoayong0309@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ayong Cao, MD
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Breast Surgery, Cancer Hospital, Fudan University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ayong Cao

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Mutation of BRCA1/2 and Other Potential Genes in Triple-negative Breast Cancer

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