A Trial of Camrelizumab Combined With Ablation and Chemotherapy in Patients With Pancreatic Cancer Liver Metastasis(SHR-1210-HLJ-009)
Primary Purpose
Pancreatic Cancer, Liver Metastasis
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Camrelizumab
Chemotherapy
Ablation
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with liver metastasis of pancreatic cancer diagnosed by histology or cytology;
- Must have CT or MRI examination in the last 3 months;
- With measurable tumor lesions (spiral CT scan ≥10mm, meet RECIST 1.1 standard);
- Expected survival time> 3 months;
- The interval between the end of the patient's previous chemotherapy or adjuvant chemotherapy must be more than 6 months;
- No radiation therapy (unless there is at least one measurable target lesion in the non-irradiated area);
- Must score pain;
- Age: 18 to 70 years old, male or female;
- ECOG PS: 0-1 points;
The functions of important organs meet the following requirements:
- Absolute neutrophil count ≥1.5×109/L, platelet ≥100×109/L, hemoglobin ≥9g/dL;
- Bilirubin ≤ 1.5 times ULN (patients drained by retrograde technique may be included); ALT and AST ≤ 5 times ULN;
- Creatinine <120 μmol/L, or MDRD creatinine clearance rate> 60 mL/min;
- Women of childbearing age must undergo a negative pregnancy test (βHCG) before starting treatment. Women and men of childbearing age (sexual relationships with women of childbearing age) must agree to use them effectively during treatment and 6 months after the last dose of treatment Contraceptive measures;
- Signature of patient information and informed consent.
Exclusion Criteria:
- Women who are pregnant or nursing, or have fertility but refuse to take contraceptive measures;
- During the enrollment period, a serious active infection requiring antibiotic intravenous treatment occurred;
- Those who are allergic to test drugs;
- Presence of ≥2 grade neuropathy (CTCAE 5.0);
- Uncontrolled, symptomatic brain metastases or those with a history of difficult-to-control mental illness or severe intellectual or cognitive dysfunction;
- Suffering from active, known or suspected autoimmune diseases (including but not limited to: uveitis, enteritis, hepatitis, pituitary inflammation, nephritis, vasculitis, hyperthyroidism, hypothyroidism and the need for bronchodilators Treatment of asthma, etc.). Subjects with hypothyroidism who only need hormone replacement therapy and skin diseases that do not require systemic treatment (such as vitiligo, psoriasis, or hair loss) can be selected;
- Have been vaccinated or will be vaccinated with live vaccine within 30 days before the administration of Camrelizumab;
- Congestive heart failure, uncontrolled arrhythmia, myocardial infarction, unstable angina, stroke or transient ischemic attack within 6 months; or other patients who cannot tolerate surgery;
- Suffering from other malignant tumors within 5 years, except for fully treated cervical carcinoma in situ or squamous cell carcinoma of the skin, or basal cell carcinoma of the skin that has been basically controlled;
- Patients who cannot comply with the trial protocol or cannot cooperate with follow-up;
- The patient has already participated in another clinical trial;
- People deprived of their liberty or guardianship;
- Unable to receive medical supervision during the trial due to geographical, social or psychological reasons;
- Patients who cannot follow the trial protocol or cannot cooperate with follow-up;
- The researchers believe that it is not appropriate to participate in this experiment.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Camrelizumab combined with ablation and chemotherapy
Arm Description
First, patients with liver metastases from pancreatic cancer are given ablation of liver metastases, and conventional chemotherapy plus camrelizumab is performed 1 week after surgery. If patients have multiple metastases, ablation treatment needs to be performed in stages, each ablation After 1 week of treatment, sequential chemotherapy + camrelizumab were reinfused, and the efficacy was evaluated every 2 cycles until the disease progressed or the patient could not tolerate it.
Outcomes
Primary Outcome Measures
6-month PFS rate
6-month progression-free survival rate
Secondary Outcome Measures
ORR
Overall Response Rate
DCR
Disease Control Rate
PFS
Progression Free Survival
Incidence of Treatment-Emergent Adverse Events
adverse events/serious adverse events
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04420130
Brief Title
A Trial of Camrelizumab Combined With Ablation and Chemotherapy in Patients With Pancreatic Cancer Liver Metastasis(SHR-1210-HLJ-009)
Official Title
Camrelizumab Combined With Ablation and Chemotherapy in Patients With Pancreatic Cancer Liver Metastasis: a Single-arm, Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Withdrawn
Why Stopped
Failed to pass ethics committee review
Study Start Date
August 1, 2020 (Anticipated)
Primary Completion Date
August 1, 2022 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Yanqiao Zhang
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
This is a a single-arm, prospective study of Camrelizumab combined with ablation and chemotherapy for patients with Pancreatic cancer liver metastasis.
The main purpose of this study is to evaluate the safety and tolerability of Camrelizumab combined with ablation and chemotherapy as a treatment of Pancreatic cancer liver metastasis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer, Liver Metastasis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Camrelizumab combined with ablation and chemotherapy
Arm Type
Experimental
Arm Description
First, patients with liver metastases from pancreatic cancer are given ablation of liver metastases, and conventional chemotherapy plus camrelizumab is performed 1 week after surgery. If patients have multiple metastases, ablation treatment needs to be performed in stages, each ablation After 1 week of treatment, sequential chemotherapy + camrelizumab were reinfused, and the efficacy was evaluated every 2 cycles until the disease progressed or the patient could not tolerate it.
Intervention Type
Drug
Intervention Name(s)
Camrelizumab
Intervention Description
Camrelizumab was administered 200mg iv every 3 weeks
Intervention Type
Drug
Intervention Name(s)
Chemotherapy
Intervention Description
The chemotherapy regimen may be a standard regimen for routine treatment of advanced pancreatic cancer.
Intervention Type
Procedure
Intervention Name(s)
Ablation
Intervention Description
First give pancreatic cancer patients with liver metastases to ablation of liver metastases
Primary Outcome Measure Information:
Title
6-month PFS rate
Description
6-month progression-free survival rate
Time Frame
From date of starting treatment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months.
Secondary Outcome Measure Information:
Title
ORR
Description
Overall Response Rate
Time Frame
From the first drug administration up to two years
Title
DCR
Description
Disease Control Rate
Time Frame
From the first drug administration up to two years
Title
PFS
Description
Progression Free Survival
Time Frame
From the first drug administration up to two years
Title
Incidence of Treatment-Emergent Adverse Events
Description
adverse events/serious adverse events
Time Frame
from the first drug administration to within 90 days for the last Camrelizumab combined with ablation and chemotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with liver metastasis of pancreatic cancer diagnosed by histology or cytology;
Must have CT or MRI examination in the last 3 months;
With measurable tumor lesions (spiral CT scan ≥10mm, meet RECIST 1.1 standard);
Expected survival time> 3 months;
The interval between the end of the patient's previous chemotherapy or adjuvant chemotherapy must be more than 6 months;
No radiation therapy (unless there is at least one measurable target lesion in the non-irradiated area);
Must score pain;
Age: 18 to 70 years old, male or female;
ECOG PS: 0-1 points;
The functions of important organs meet the following requirements:
Absolute neutrophil count ≥1.5×109/L, platelet ≥100×109/L, hemoglobin ≥9g/dL;
Bilirubin ≤ 1.5 times ULN (patients drained by retrograde technique may be included); ALT and AST ≤ 5 times ULN;
Creatinine <120 μmol/L, or MDRD creatinine clearance rate> 60 mL/min;
Women of childbearing age must undergo a negative pregnancy test (βHCG) before starting treatment. Women and men of childbearing age (sexual relationships with women of childbearing age) must agree to use them effectively during treatment and 6 months after the last dose of treatment Contraceptive measures;
Signature of patient information and informed consent.
Exclusion Criteria:
Women who are pregnant or nursing, or have fertility but refuse to take contraceptive measures;
During the enrollment period, a serious active infection requiring antibiotic intravenous treatment occurred;
Those who are allergic to test drugs;
Presence of ≥2 grade neuropathy (CTCAE 5.0);
Uncontrolled, symptomatic brain metastases or those with a history of difficult-to-control mental illness or severe intellectual or cognitive dysfunction;
Suffering from active, known or suspected autoimmune diseases (including but not limited to: uveitis, enteritis, hepatitis, pituitary inflammation, nephritis, vasculitis, hyperthyroidism, hypothyroidism and the need for bronchodilators Treatment of asthma, etc.). Subjects with hypothyroidism who only need hormone replacement therapy and skin diseases that do not require systemic treatment (such as vitiligo, psoriasis, or hair loss) can be selected;
Have been vaccinated or will be vaccinated with live vaccine within 30 days before the administration of Camrelizumab;
Congestive heart failure, uncontrolled arrhythmia, myocardial infarction, unstable angina, stroke or transient ischemic attack within 6 months; or other patients who cannot tolerate surgery;
Suffering from other malignant tumors within 5 years, except for fully treated cervical carcinoma in situ or squamous cell carcinoma of the skin, or basal cell carcinoma of the skin that has been basically controlled;
Patients who cannot comply with the trial protocol or cannot cooperate with follow-up;
The patient has already participated in another clinical trial;
People deprived of their liberty or guardianship;
Unable to receive medical supervision during the trial due to geographical, social or psychological reasons;
Patients who cannot follow the trial protocol or cannot cooperate with follow-up;
The researchers believe that it is not appropriate to participate in this experiment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanqiao Zhang, PhD
Organizational Affiliation
Harbin Medical University Cancer Hosptital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
A Trial of Camrelizumab Combined With Ablation and Chemotherapy in Patients With Pancreatic Cancer Liver Metastasis(SHR-1210-HLJ-009)
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