CIK in Treating Patients With Bladder Cancer

Sponsor
The First People's Hospital of Changzhou (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02489890
Collaborator
(none)
1,500
2
172.9

Study Details

Study Description

Brief Summary

Chemotherapy is the main treatment method for patients with Bladder Cancer. However, Relapse remains the major cause of treatment failure.Biological therapies such as CIK stimulate the immune system and stop tumor cells from growing. A series of studies reported that cytokine-induced killer cells (CIK) have a broad anti-tumor spectrum. The investigators suppose that CIK will improve the prognosis. Combining chemotherapy with biological therapy may kill more tumor cells. In this study, the patients will be treated with CIK cells after chemotherapy. The purpose of this study is to evaluate the efficacy of CIK for Bladder Cancer.

Condition or Disease Intervention/Treatment Phase
  • Biological: Cytokine-induced Killer Cells
Phase 2

Detailed Description

About 1500 patients with staging I-III of Bladder Cancer, after accepting chemotherapy, will be randomly divided into group A (receive CIK treatment) or group B (just regularly follow up), and the randomize ratio will be 1:1. Patients in group A will receive 3 cycles of CIK cells treatment (every 12 weeks). Patients in group B will have no anti-tumor therapy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomized Controlled Study of Cytokine-induced Killer Cells (CIK) Treatment in Patients With Staging Ⅰ-Ⅲ of Urinary Bladder Carcinoma
Study Start Date :
Feb 1, 2016
Anticipated Primary Completion Date :
Jul 1, 2025
Anticipated Study Completion Date :
Jul 1, 2030

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Non-CIK

After accepting chemotherapy, patients will regularly follow up.

Experimental: CIK

After accepting chemotherapy, patients will receive at least 3 cycles of Cytokine-induced Killer Cells treatment per year.

Biological: Cytokine-induced Killer Cells
chemotherapy plus 3 cycles of Cytokine-induced Killer Cells(CIK) treatment
Other Names:
  • CIK
  • Outcome Measures

    Primary Outcome Measures

    1. progression-free survival(PFS) [1 month]

    Secondary Outcome Measures

    1. overall survival(OS) [1 month]

    Other Outcome Measures

    1. age [1 week]

      by years

    2. gender [1 week]

      men or women

    3. Performance status [1 week]

      WHO standard

    4. number of sites of extranodal involvement [1 week]

      evaluated by CT scan

    5. Stage at diagnosis [1 week]

      Tumor Node Metastasis (TNM) stage, Tumor:CIS,T1,T2,T3,T4 according to the depth of tumor invasion. Lymph node involvement: N0,N1,N2. Metastasis: M0,M1

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients histologically confirmed carcinoma in of the bladder with urinary cytology;

    • Patients with staging I-III of Bladder Cancer;

    • Patients who had completed chemotherapy;

    • Patients who have a life expectancy of at least 12 weeks;

    • Eastern Cooperative Oncology Group (ECOG) performance status was 0-1;

    • The bone marrow functioned normally (WBC>4.0×109/L, Hb>120 g/L, Platelet(PLT)>100×109/L);

    • The ECG results were normal, and the liver and kidney were functional.

    Exclusion Criteria:
    • Patients who had upper urinary tract disease (e.g., vesico-ureteral reflux or massive stones) that would make multiple transurethral procedures risk;

    • Patients who had urethral strictures that would prevent endoscopic procedures and repeated catheterization;

    • Patients who had prior or concurrent upper urinary tract tumors;

    • Patients who had distant metastases by imaging studies;

    • Patients with uncontrolled infection; underlying disease that was severe or life-threatening;

    • Patients who were lactating;

    • ECOG perform status ≥ 2;

    • Patients who are suffering from auto immune diseases or patients who need to accept glucocorticoid treatment;

    • Patients who are pregnant or nursing;

    • Patients with active tuberculosis (highly positive skin tests allowed if no active disease);

    • Patients with disease that would preclude general anesthesia;

    • Patients with active intractable or uncontrollable infection.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • The First People's Hospital of Changzhou

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    The First People's Hospital of Changzhou
    ClinicalTrials.gov Identifier:
    NCT02489890
    Other Study ID Numbers:
    • BLAD001
    First Posted:
    Jul 3, 2015
    Last Update Posted:
    Feb 22, 2016
    Last Verified:
    Feb 1, 2016
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 22, 2016