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CIK in Treating Patients With Bladder Cancer

A Randomized Controlled Study of Cytokine-induced Killer Cells (CIK) Treatment in Patients With Staging Ⅰ-Ⅲ of Urinary Bladder Carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02489890
Enrollment
1500
Registered
2015-07-03
Start date
2016-02-29
Completion date
2030-07-31
Last updated
2016-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Bladder Neoplasms

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.

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.

Interventions

chemotherapy plus 3 cycles of Cytokine-induced Killer Cells(CIK) treatment

Sponsors

The First People's Hospital of Changzhou
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
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\>4.0×10\^9/L, Hb\>120 g/L, Platelet(PLT)\>100×10\^9/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.

Design outcomes

Primary

MeasureTime frame
progression-free survival(PFS)1 month

Secondary

MeasureTime frame
overall survival(OS)1 month

Other

MeasureTime frameDescription
Performance status1 weekWHO standard
age1 weekby years
Stage at diagnosis1 weekTumor 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
number of sites of extranodal involvement1 weekevaluated by CT scan
gender1 weekmen or women

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026