search
Back to results

A Phase II Clinical Study of Treatment With Disitamb Vedotin Plus Pyrotinib in HER2-positive Early Breast Cancer

Primary Purpose

Breast Cancer

Status
Not yet recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Disitamb Vedotin ,pyrotinib
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring HER2-positive, RC48

Eligibility Criteria

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

Inclusion Criteria: 1.18 to 75 years old (at the time of signing the informed consent form), regardless of gender. 2. Subject type and disease characteristics. Histologically confirmed HER2 positive EBC subjects: (a) evaluated as HER2 positive in local laboratories according to ASCOCAP guidelines. (b) Single and multifocal tumors (greater than 1 tumor area limited to the same quadrant as the primary tumor) must be sampled from 1 lesion and laboratory confirmed as HER2 positive. (c) Multicenter tumors (multiple tumors involving more than one breast quadrant) must sample one lesion from each affected quadrant and be confirmed as HER2 positive by the central laboratory. (d) According to ASCOCAP guidelines, tumors are either HR positive or HR negative (ER and PgR negative). (e) Clinical staging at visit (based on breast X-ray or breast MRI evaluation): Stage II-IIIC determined by the AJCC staging system, 8th edition. (f) Lymph node involvement is determined by fine needle aspiration or coarse needle aspiration biopsy (if applicable). 3. When randomized, ECOG physical fitness status is 0 or 1 point. Exclusion Criteria: Previous history of invasive breast cancer. Stage IV breast cancer according to AJCC staging system version 8. Within 3 years, there is any primary malignant tumor, except for fully resected non-melanoma skin cancer or cured in situ disease. DCIS medical history, except for the subjects who only received Mastectomy According to the judgment of the researchers, there is evidence of any diseases (such as severe or uncontrolled systemic diseases, including persistent or active infections, uncontrolled hypertension, kidney transplantation and active bleeding diseases, and severe chronic gastrointestinal diseases related to diarrhea) that the researchers consider to be unfavorable for the participants to participate in the study or may affect adherence to the protocol. Uncontrolled infection requiring intravenous administration of antibiotics, Antiviral drug or antifungal drugs.

Sites / Locations

  • Jiangsu Provincial People's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Disitamb Vedotin combined with pyrotinib

Arm Description

Disitamb Vedotin: 2 mg/kg,ivgtt,d1,14/28day/cycle pyrotinib:320mg, oral, every day.

Outcomes

Primary Outcome Measures

pathologic complete response(pCR)
The pCR rate is defined as the proportion of subjects who, after completion of neoadjuvant therapy, showed no evidence of residual invasive lesions in H&E staining in completely excised breast specimens and all sampled local lymph nodes (ypT0/TisypN0) through central evaluation

Secondary Outcome Measures

Disease free survival (DFS)
Breast-conserving surgery(BCS)
The Number of Participants Who Experienced Adverse Events (AE)
Residual Cancer Burden(RCB)
Health-related quality of life(HRQoL)questionnaire

Full Information

First Posted
August 14, 2023
Last Updated
August 18, 2023
Sponsor
The First Affiliated Hospital with Nanjing Medical University
search

1. Study Identification

Unique Protocol Identification Number
NCT06001086
Brief Title
A Phase II Clinical Study of Treatment With Disitamb Vedotin Plus Pyrotinib in HER2-positive Early Breast Cancer
Official Title
A Multicenter, Open Phase II Clinical Study to Evaluate the Efficacy and Safety of Disitamb Vedotin Combined With Pyrotinib in Previously Untreated Histologically Proven HER2 Positive Early Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 21, 2023 (Anticipated)
Primary Completion Date
August 1, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University

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
Evaluate the efficacy and safety of Disitamb Vedotin combined with pyrotinib in HER2 positive early breast cancer
Detailed Description
The main goal of this clinical trial is to evaluate the efficacy of Disitamb Vedotin combined with pyrotinib in previously untreated histologically proven HER2 positive early breast cancer and evaluate the PCR DFS,OS and safety of the subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
HER2-positive, RC48

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Disitamb Vedotin combined with pyrotinib
Arm Type
Experimental
Arm Description
Disitamb Vedotin: 2 mg/kg,ivgtt,d1,14/28day/cycle pyrotinib:320mg, oral, every day.
Intervention Type
Drug
Intervention Name(s)
Disitamb Vedotin ,pyrotinib
Other Intervention Name(s)
Regular Visits
Intervention Description
Disitamb Vedotin combined with pyrotinib
Primary Outcome Measure Information:
Title
pathologic complete response(pCR)
Description
The pCR rate is defined as the proportion of subjects who, after completion of neoadjuvant therapy, showed no evidence of residual invasive lesions in H&E staining in completely excised breast specimens and all sampled local lymph nodes (ypT0/TisypN0) through central evaluation
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Disease free survival (DFS)
Time Frame
3 years
Title
Breast-conserving surgery(BCS)
Time Frame
Intraoperative
Title
The Number of Participants Who Experienced Adverse Events (AE)
Time Frame
1 year
Title
Residual Cancer Burden(RCB)
Time Frame
3 years
Title
Health-related quality of life(HRQoL)questionnaire
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1.18 to 75 years old (at the time of signing the informed consent form), regardless of gender. 2. Subject type and disease characteristics. Histologically confirmed HER2 positive EBC subjects: (a) evaluated as HER2 positive in local laboratories according to ASCOCAP guidelines. (b) Single and multifocal tumors (greater than 1 tumor area limited to the same quadrant as the primary tumor) must be sampled from 1 lesion and laboratory confirmed as HER2 positive. (c) Multicenter tumors (multiple tumors involving more than one breast quadrant) must sample one lesion from each affected quadrant and be confirmed as HER2 positive by the central laboratory. (d) According to ASCOCAP guidelines, tumors are either HR positive or HR negative (ER and PgR negative). (e) Clinical staging at visit (based on breast X-ray or breast MRI evaluation): Stage II-IIIC determined by the AJCC staging system, 8th edition. (f) Lymph node involvement is determined by fine needle aspiration or coarse needle aspiration biopsy (if applicable). 3. When randomized, ECOG physical fitness status is 0 or 1 point. Exclusion Criteria: Previous history of invasive breast cancer. Stage IV breast cancer according to AJCC staging system version 8. Within 3 years, there is any primary malignant tumor, except for fully resected non-melanoma skin cancer or cured in situ disease. DCIS medical history, except for the subjects who only received Mastectomy According to the judgment of the researchers, there is evidence of any diseases (such as severe or uncontrolled systemic diseases, including persistent or active infections, uncontrolled hypertension, kidney transplantation and active bleeding diseases, and severe chronic gastrointestinal diseases related to diarrhea) that the researchers consider to be unfavorable for the participants to participate in the study or may affect adherence to the protocol. Uncontrolled infection requiring intravenous administration of antibiotics, Antiviral drug or antifungal drugs.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wei Li, Ph.D
Phone
025-68307102
Email
real.lw@163.com
Facility Information:
Facility Name
Jiangsu Provincial People's Hospital
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Phase II Clinical Study of Treatment With Disitamb Vedotin Plus Pyrotinib in HER2-positive Early Breast Cancer

We'll reach out to this number within 24 hrs