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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Withdrawn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
Yanqiao Zhang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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:

    1. Absolute neutrophil count ≥1.5×109/L, platelet ≥100×109/L, hemoglobin ≥9g/dL;
    2. Bilirubin ≤ 1.5 times ULN (patients drained by retrograde technique may be included); ALT and AST ≤ 5 times ULN;
    3. 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

    First Posted
    June 3, 2020
    Last Updated
    October 1, 2022
    Sponsor
    Yanqiao Zhang
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    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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