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Disitamab Vedotin Combined With Tislelizumab in Advanced HER2 Positive Colorectal Cancer

Primary Purpose

Colorectal Neoplasms

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Disitamab vedotin
Tislelizumab
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 Colorectal Neoplasms focused on measuring Colorectal Cancer, Antibody Drug Conjugate, Disitamab Vedotin, Tislelizumab

Eligibility Criteria

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

Inclusion Criteria:

  1. Signed the consents voluntarily;
  2. All genders, age 18 or above;
  3. Histological or cytological documentation of local advanced or metastatic unresectable colorectal carcinoma;
  4. Patients with HER-2 overexpression (HER-2 IHC 2+ or IHC 3+) detected by immunohistochemistry; Resampling is recommended for samples over 3 years.
  5. Subjects must have failed at treatments including fluoropyrimidine, oxaliplatin and irinotecan; For adjuvant or neoadjuvant chemotherapy, if disease progression occurs during treatment or within 6 months after treatment, it will be recorded as a first-line treatment;
  6. Patients who have used anti-PD-1 or anti-PD-L1 inhibitors can be selected after stopping the treatment for more than 6 months; Patients who have used other anti HER-2 drugs with different mechanisms can be selected.
  7. Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria, version 1.1.is necessary
  8. Life expectancy of at least 3 months.
  9. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1.
  10. Have sufficient heart, lung, liver and kidney functions, and the laboratory examination within 14 days before screening meets the following indicators:

    i. Hemoglobin Hb ≥ 90 g/L ii. Neutrophil count ANC ≥ 1.5*10^9 /L iii. Platelet count PLT ≥ 80*10^9 /L iv. Albumin ALB ≥ 35 g/L v. Alanine aminotransferase ALT and aspartate aminotransferase AST ≤ 2.5 times the upper limit of the normal range, and liver metastasis patients ≤ 5 times the upper limit of the normal range.

    vi. Total bilirubin ≤ 1.5 times, or 2 times the upper limit of normal. vii. Creatinine Scr ≤ upper limit of normal range. viii. Prothrombin: PT-INR ≤ 2.3 or PT < 6 seconds compared with normal control

  11. Subjects must complete the treatment and follow-up on schedule. according to the research plan.
  12. No brain metastasis, no spinal cord compression.
  13. Subjects agree to use blood samples for study analysis.
  14. Women of childbearing age must be negative in pregnancy test and willing to take effective contraceptive measures during the study period.

Exclusion Criteria:

  1. Subjects are severe malnutrition or need tube feeding.
  2. Major surgery has been performed within 30 days before treatment.
  3. Previous treatment with anti-PD-1 / PD-L1 inhibitor, anti-CTLA-4 inhibitor, ADC drugs targeting HER-2 such as RC48 and T-DM1 within 6 months.
  4. Other malignant tumors within 2 years and without cure (Except for patients with other early-stage tumors, after radical treatment, whom the researchers assess the recurrence risk of in the short term is small);
  5. Subjects have active autoimmune system diseases that need systemic hormone therapy or anti autoimmune drug therapy.
  6. Subjects with immunodeficiency or receiving systemic steroid therapy (prednisone > 10 mg / day or other equivalent drugs) or other forms of immunosuppressive therapy 7 days before the first dose of combination therapy in this study;
  7. Subjects with active infection and still need systemic treatment 7 days before the first dose of therapy in this study.
  8. Subjects with uncontrollable systemic diabetes.
  9. Subjects with interstitial lung disease, non infectious pneumonia or pulmonary fibrosis;
  10. Subjects who have received allogeneic organ or stem cell transplantation in the past.
  11. Subjects allergic to the drugs or related components involved in this study.
  12. Participating in other interventional clinical studies.
  13. The previous anti-tumor related adverses do not return to grade 1 in CTCAE before the first combination therapy.
  14. Subjects who have uncontrolled hypertension by drugs, that is, systolic blood pressure ≥ 140 mmHg and / or diastolic blood pressure ≥ 90 mmHg.
  15. Thrombotic or hemorrhagic tendency or history within 60 days before the first medication, regardless of the severity.
  16. Any serious or unstable medical condition#mental illness or known active alcohol or drug abuse or dependence.

Sites / Locations

  • Changzhou NO.2 People's HospitalRecruiting
  • The Affiliated Huaian No.1 People's Hospital of Nanjing Medical UniversityRecruiting
  • The First Affiliated Hospital with Nanjing Medical UniversityRecruiting
  • the Third Affiliated Hospital of Soochow UniversityRecruiting
  • Xuzhou Central HospitalRecruiting
  • Fudan University Shanghai Cancer CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Combination of Disitamab Vedotin and Tislelizumab

Arm Description

Disitamab Vedotin 2.0mg/kg q2w+Tislelizumab 400mg q6w. The treatment of Disitamab Vedotin + Tislelizumab will continue until the tumor progression confirmed by imaging, or up to 2 years, or intolerable toxic reactions, or other conditions determined by the researchers.

Outcomes

Primary Outcome Measures

Objective response rate(ORR)
The percentage of subjects with total number of Complete Response (CR) + total number of Partial Response (PR)

Secondary Outcome Measures

Progression-free Survival(PFS)
PFS was defined as the time from assignment to disease progression radiological/clinical or death due to any cause, whichever occurs first. Subjects without progression or death at the time of analysis were censored at their last date of tumor evaluation.
Overall Survival (OS)
OS is defined as the time from date of assignment to death due to any cause. Subjects still alive at the time of analysis were censored at their last date of last contact.
Disease control rate (DCR)
DCR is defined as the percentage of subjects whose best response was not Progressive Disease (PD) according to Response Evaluation Criteria in Solid Tumors (RECIST) (= total number of Complete Response (CR) + total number of Partial Response (PR) + total number of Stable Disease (SD).
Safety and Feasibility
Safety is defined as the incidence of Grade 3-4 Treatment-Related Adverse Events (TRAEs) from the day of neoadjuvant therapy to 30 days after surgery or within 90 days after last neoadjuvant treatment. Feasibility of surgery is defined as the incidence of TRAEs causing surgery delay of ≥30 days and/or inoperable patients.Feasibility of surgery is defined as the incidence of TRAEs causing surgery delay of ≥30 days and/or inoperable patients.
Duration of Response (DOR)
DOR is defined as the time from randomization to disease progression or death in patients who achieve complete or partial response.

Full Information

First Posted
August 7, 2022
Last Updated
October 19, 2022
Sponsor
The First Affiliated Hospital with Nanjing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT05493683
Brief Title
Disitamab Vedotin Combined With Tislelizumab in Advanced HER2 Positive Colorectal Cancer
Official Title
A Single Arm, Open Label, Multiple Center, Prospective Study of Disitamab Vedotin Combined With Tislelizumab in HER2 Positive Advanced Colorectal Cancer Failed at Least Two Lines of Systemic Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2022 (Actual)
Primary Completion Date
July 2025 (Anticipated)
Study Completion Date
July 2025 (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

5. Study Description

Brief Summary
Among patients with colonrectal cancer, 5% were HER-2 positive, but the immunohistochemical results were mostly HER-2 2 +, which did not meet the indications of HER-2 targeting drugs. Disitamab Vedotin , which was listed in China last year, achieved similar results in HER-2 2+ and 3+, according to a clinical trial for breast cancer, suggesting that patients with colonrectal cancer may benefit from it. Tislelizumab is a PD-1 monoclonal antibody, which has been approved for a variety of tumors. It was reported that anti-HER-2 treatment can improve the tumor immune microenvironment and improve the efficacy of immunotherapy. At the same time, our previous studies showed that anti-PD-1 combined with Disitamab Vedotin can significantly inhibit the growth of colon tumor in mice. Therefore, Disitamab Vedotin and Tislelizumab were used in this study. This prospective clinical trial may bring new hope for the treatment of HER-2 positive CRC patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms
Keywords
Colorectal Cancer, Antibody Drug Conjugate, Disitamab Vedotin, Tislelizumab

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Combination of Disitamab Vedotin and Tislelizumab
Arm Type
Experimental
Arm Description
Disitamab Vedotin 2.0mg/kg q2w+Tislelizumab 400mg q6w. The treatment of Disitamab Vedotin + Tislelizumab will continue until the tumor progression confirmed by imaging, or up to 2 years, or intolerable toxic reactions, or other conditions determined by the researchers.
Intervention Type
Drug
Intervention Name(s)
Disitamab vedotin
Other Intervention Name(s)
RC48
Intervention Description
2.0mg/kg,q2w
Intervention Type
Drug
Intervention Name(s)
Tislelizumab
Intervention Description
400mg,q6w
Primary Outcome Measure Information:
Title
Objective response rate(ORR)
Description
The percentage of subjects with total number of Complete Response (CR) + total number of Partial Response (PR)
Time Frame
up to 2 years
Secondary Outcome Measure Information:
Title
Progression-free Survival(PFS)
Description
PFS was defined as the time from assignment to disease progression radiological/clinical or death due to any cause, whichever occurs first. Subjects without progression or death at the time of analysis were censored at their last date of tumor evaluation.
Time Frame
From date of subjects until the date of first documented progression or death from any cause, whichever came first, assessed up to 24 months
Title
Overall Survival (OS)
Description
OS is defined as the time from date of assignment to death due to any cause. Subjects still alive at the time of analysis were censored at their last date of last contact.
Time Frame
From assignment of the first subject until 32 death events observed, up to 2 years.
Title
Disease control rate (DCR)
Description
DCR is defined as the percentage of subjects whose best response was not Progressive Disease (PD) according to Response Evaluation Criteria in Solid Tumors (RECIST) (= total number of Complete Response (CR) + total number of Partial Response (PR) + total number of Stable Disease (SD).
Time Frame
up to 2 years
Title
Safety and Feasibility
Description
Safety is defined as the incidence of Grade 3-4 Treatment-Related Adverse Events (TRAEs) from the day of neoadjuvant therapy to 30 days after surgery or within 90 days after last neoadjuvant treatment. Feasibility of surgery is defined as the incidence of TRAEs causing surgery delay of ≥30 days and/or inoperable patients.Feasibility of surgery is defined as the incidence of TRAEs causing surgery delay of ≥30 days and/or inoperable patients.
Time Frame
up to 2 years
Title
Duration of Response (DOR)
Description
DOR is defined as the time from randomization to disease progression or death in patients who achieve complete or partial response.
Time Frame
up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed the consents voluntarily; All genders, age 18 or above; Histological or cytological documentation of local advanced or metastatic unresectable colorectal carcinoma; Patients with HER-2 overexpression (HER-2 IHC 2+ or IHC 3+) detected by immunohistochemistry; Resampling is recommended for samples over 3 years. Subjects must have failed at treatments including fluoropyrimidine, oxaliplatin and irinotecan; For adjuvant or neoadjuvant chemotherapy, if disease progression occurs during treatment or within 6 months after treatment, it will be recorded as a first-line treatment; Patients who have used anti-PD-1 or anti-PD-L1 inhibitors can be selected after stopping the treatment for more than 6 months; Patients who have used other anti HER-2 drugs with different mechanisms can be selected. Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria, version 1.1.is necessary Life expectancy of at least 3 months. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1. Have sufficient heart, lung, liver and kidney functions, and the laboratory examination within 14 days before screening meets the following indicators: i. Hemoglobin Hb ≥ 90 g/L ii. Neutrophil count ANC ≥ 1.5*10^9 /L iii. Platelet count PLT ≥ 80*10^9 /L iv. Albumin ALB ≥ 35 g/L v. Alanine aminotransferase ALT and aspartate aminotransferase AST ≤ 2.5 times the upper limit of the normal range, and liver metastasis patients ≤ 5 times the upper limit of the normal range. vi. Total bilirubin ≤ 1.5 times, or 2 times the upper limit of normal. vii. Creatinine Scr ≤ upper limit of normal range. viii. Prothrombin: PT-INR ≤ 2.3 or PT < 6 seconds compared with normal control Subjects must complete the treatment and follow-up on schedule. according to the research plan. No brain metastasis, no spinal cord compression. Subjects agree to use blood samples for study analysis. Women of childbearing age must be negative in pregnancy test and willing to take effective contraceptive measures during the study period. Exclusion Criteria: Subjects are severe malnutrition or need tube feeding. Major surgery has been performed within 30 days before treatment. Previous treatment with anti-PD-1 / PD-L1 inhibitor, anti-CTLA-4 inhibitor, ADC drugs targeting HER-2 such as RC48 and T-DM1 within 6 months. Other malignant tumors within 2 years and without cure (Except for patients with other early-stage tumors, after radical treatment, whom the researchers assess the recurrence risk of in the short term is small); Subjects have active autoimmune system diseases that need systemic hormone therapy or anti autoimmune drug therapy. Subjects with immunodeficiency or receiving systemic steroid therapy (prednisone > 10 mg / day or other equivalent drugs) or other forms of immunosuppressive therapy 7 days before the first dose of combination therapy in this study; Subjects with active infection and still need systemic treatment 7 days before the first dose of therapy in this study. Subjects with uncontrollable systemic diabetes. Subjects with interstitial lung disease, non infectious pneumonia or pulmonary fibrosis; Subjects who have received allogeneic organ or stem cell transplantation in the past. Subjects allergic to the drugs or related components involved in this study. Participating in other interventional clinical studies. The previous anti-tumor related adverses do not return to grade 1 in CTCAE before the first combination therapy. Subjects who have uncontrolled hypertension by drugs, that is, systolic blood pressure ≥ 140 mmHg and / or diastolic blood pressure ≥ 90 mmHg. Thrombotic or hemorrhagic tendency or history within 60 days before the first medication, regardless of the severity. Any serious or unstable medical condition#mental illness or known active alcohol or drug abuse or dependence.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yanhong Gu, Dr
Phone
00862568306714
Email
guluer@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Shiyun Cui, Dr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gu Yanhong
Organizational Affiliation
The First Affiliated Hospital with Nanjing Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Changzhou NO.2 People's Hospital
City
Changzhou
State/Province
Jiangsu
ZIP/Postal Code
150000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hua Jiang
Facility Name
The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University
City
Huai'an
State/Province
Jiangsu
ZIP/Postal Code
150000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaomin Zhong
Facility Name
The First Affiliated Hospital with Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanhong Gu, Ph.D
Phone
13813908678
Email
guluer@163.com
First Name & Middle Initial & Last Name & Degree
Yanhong Gu, Ph.D
Facility Name
the Third Affiliated Hospital of Soochow University
City
Suzhou
State/Province
Jiangsu
ZIP/Postal Code
150000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wenwei Hu
Facility Name
Xuzhou Central Hospital
City
Xuzhou
State/Province
Jiangsu
ZIP/Postal Code
150000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuan Yuan
Facility Name
Fudan University Shanghai Cancer Center
City
Shanghai
State/Province
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhiyu Chen

12. IPD Sharing Statement

Plan to Share IPD
No
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Disitamab Vedotin Combined With Tislelizumab in Advanced HER2 Positive Colorectal Cancer

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