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DC Vaccine Combined With CIK Cells in Patients With SCLC

Primary Purpose

Small- Cell Lung Cancer

Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
adenovirus-transfected autologous DC vaccine plus CIK cells
Sponsored by
Affiliated Hospital to Academy of Military Medical Sciences
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small- Cell Lung Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Histopathologically confirmed diagnosis of Small- Cell Lung Cancer
  • Age >18 years at time of consent
  • Received standardized treatment of Small-Cell Lung Cancer
  • Interval between the last standardized treatment and DC/CIK treatment ≥ 4weeks
  • KPS (Karnofsky performance scale) >60
  • Patient's written informed consent
  • No severe viral or bacterial infections
  • Predicted survival >3 months

Exclusion Criteria:

  • Clinically relevant diseases or infections (HBV, HCV, HIV)
  • Females who are pregnant or nursing
  • Immunosuppressant treatment
  • Currently participating in another clinical trial
  • Unfit for participating in this clinical trial in investigators' opinions

Sites / Locations

    Outcomes

    Primary Outcome Measures

    objective rate response (CR+PR) as measured by RECIST criteria

    Secondary Outcome Measures

    number of participants with adverse events

    Full Information

    First Posted
    February 18, 2016
    Last Updated
    February 18, 2016
    Sponsor
    Affiliated Hospital to Academy of Military Medical Sciences
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02688673
    Brief Title
    DC Vaccine Combined With CIK Cells in Patients With SCLC
    Official Title
    Safety and Therapeutic Efficacy of DC Vaccine Combined With Cytokine-induced Killer Cells in Patients With Extensive-Stage Small- Cell Lung Cancer: a Phase I/II Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 2014 (undefined)
    Primary Completion Date
    August 2016 (Anticipated)
    Study Completion Date
    November 2016 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Affiliated Hospital to Academy of Military Medical Sciences

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The aim of this study is to evaluate the safety and efficacy of dendritic cells (DC) combined with cytokine-induced killer (CIK) cells treatment patients with Extensive-Stage Small-Cell Lung Cancer. Experimental adopted recombinant adenovirus-code MUC1 and Survivin transfected DC, which are used for DC-based immunotherapy. Based on the results of our previously preclinical research with DC combined with CIK cells, the investigators plan to perform the clinical trial.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Small- Cell Lung Cancer

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Biological
    Intervention Name(s)
    adenovirus-transfected autologous DC vaccine plus CIK cells
    Primary Outcome Measure Information:
    Title
    objective rate response (CR+PR) as measured by RECIST criteria
    Time Frame
    4 weeks after DC/CIK treatment]
    Secondary Outcome Measure Information:
    Title
    number of participants with adverse events
    Time Frame
    3 days within DC/CIK treatment

    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: Histopathologically confirmed diagnosis of Small- Cell Lung Cancer Age >18 years at time of consent Received standardized treatment of Small-Cell Lung Cancer Interval between the last standardized treatment and DC/CIK treatment ≥ 4weeks KPS (Karnofsky performance scale) >60 Patient's written informed consent No severe viral or bacterial infections Predicted survival >3 months Exclusion Criteria: Clinically relevant diseases or infections (HBV, HCV, HIV) Females who are pregnant or nursing Immunosuppressant treatment Currently participating in another clinical trial Unfit for participating in this clinical trial in investigators' opinions

    12. IPD Sharing Statement

    Learn more about this trial

    DC Vaccine Combined With CIK Cells in Patients With SCLC

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