A Pilot Study of Radiation-Immune Cell Combination Therapy in Cervical Cancer
Primary Purpose
Uterine Cervical Neoplasms
Status
Terminated
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Immune cell
Low dose radiation
Sponsored by
About this trial
This is an interventional treatment trial for Uterine Cervical Neoplasms focused on measuring Low dose radiation, Adoptive immune cell therapy, Cervical cancer, Pilot study
Eligibility Criteria
Inclusion Criteria:
- Patients must have signed an approved informed consent and authorization permitting release of personal health information.
- Age 18-75 years
Pathologically proven recurrent or persistent cervical cancer patients resistant to conventional palliative chemotherapy or radiation therapy
- Persistent tumor more than 1cm after initial chemoradiation or radiation therapy
- Persistent tumor more than 1cm after chemoradiation, radiation or chemotherapy in recurrent cervical cancer
- Metastatic cervical cancer to lung resistant to conventional chemotherapy
- ECOG performance status 0, 1, 2.
- Expected survival more than 3 months
Patients must have adequate:
Hematologic function: ANC ≥ 1,500/mcl, Hemoglobin >10g/dL, platelets ≥ 100,000/mcl Renal function: creatinine ≤ 1.5 x ULN Hepatic function: AST, ALT ≤ 1.5 x ULN,
- More than 3 weeks from the last day of previous chemotherapy or radiation
Exclusion Criteria:
- Patients with immune disease or auto-immune disease (ex. rheumatoid arthritis, SLE, immune vasculitis, IDDM)
- Immune deficiency disease
- Cancers other than cervical cancer within 5 years
- Acute myocardial infarction, uncontrolled hypertension
- Severe allergic disease
- Severe psychotic disease
- Those who can be a candidate for curative surgery
Sites / Locations
- Sang-Young Ryu
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Low dose radiation, Immune cell therapy
Arm Description
Combination treatment of low-dose radiation 20cGy every 3 weeks three times and autologous immune cell therapy 2 consecutive weeks 3 times every 3 weeks
Outcomes
Primary Outcome Measures
Response rate
Response rate according to RECIST criteria for 12 months
Secondary Outcome Measures
Toxicity
Toxcity according to CTCSEver4.0
Full Information
NCT ID
NCT01194609
First Posted
September 2, 2010
Last Updated
May 7, 2014
Sponsor
Korea Cancer Center Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01194609
Brief Title
A Pilot Study of Radiation-Immune Cell Combination Therapy in Cervical Cancer
Official Title
A Pilot Study of Radiation-Immune Cell Combination Therapy in Recurrent or Persistent Cervical Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Terminated
Why Stopped
No further enrollment after two patients
Study Start Date
September 2010 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea Cancer Center Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Among the immune cell therapy, autologous adoptive immune cell therapy is a method to transfer the immune cells derived from peripheral white blood cells and expanded and stimulated with various cytokines and tumor specific antigens in cancer patients. Recently, the low-dose radiation is known to increase the immune response in many human cancer patients. In a clinical trial, 70% response rate with combination of low-dose radiation and adoptive immune cell therapy was reported in recurrent melanoma patients. This study is to investigate the feasibility of combination of low-dose radiation and autologous immune cell therapy in recurrent cervical cancer which is resistant to conventional palliative treatment.
Detailed Description
Immune cell therapy is considered one of the most promising anti-cancer strategy in many human cancers. Compared to the destructive methods such as surgery, radiation, and chemotherapy, anti-cancer immune therapy is safer and less toxic method in the treatment of human cancer patients.
Among the immune cell therapy, autologous adoptive immune cell therapy is a method to transfer the immune cells derived from peripheral white blood cells and expanded and stimulated with various cytokines and tumor specific antigens in cancer patients. Recent development of the technique to expand immune cells ex vivo make autologous adoptive immune cell therapy much more feasible and popular. However, immune cell therapy showed response of below 10% currently in several clinical trials. The reason of poor response is that the adopted immune cells have to overcome the highly immune compromised environment in advanced or recurrent cancer patients.
The low-dose radiation, defined as the radiation below the therapeutic dose range, is known to increase the immune response in many human cancer patients. Despite the exact mechanism is not well known, the 'danger signal' and the decrease of T-regulatory cells by low-dose radiation are the possible mechanism of enhanced immunity by low-dose radiation. So, the combination of low-dose radiation and immune cell therapy can be a attractive strategy to recurrent or advanced cancer patients who are resistant to conventional treatment.
A challenging clinical trial performed in recurrent melanoma cancers, Dr. Rosenverg reported around 70% response rate with combination of low-dose radiation and adoptive immune cell therapy. However, the feasibility of combination of low-dose radiation and immune cell therapy is still unknown in many human cancers.
This study is to investigate the feasibility of combination of low-dose radiation and autologous immune cell therapy in recurrent cervical cancer which is resistant to conventional palliative treatment. The cervical cancer, highly responsive to radiation, becomes resistant to radiation in case of recurrent disease. We hypothetize that if the low-dose radiation can reverse the immune compromised environment, adoptive immune cells derived from the autologous peripheral blood immune cells will be highly effective in recurrent cervical cancers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uterine Cervical Neoplasms
Keywords
Low dose radiation, Adoptive immune cell therapy, Cervical cancer, Pilot study
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
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low dose radiation, Immune cell therapy
Arm Type
Experimental
Arm Description
Combination treatment of low-dose radiation 20cGy every 3 weeks three times and autologous immune cell therapy 2 consecutive weeks 3 times every 3 weeks
Intervention Type
Biological
Intervention Name(s)
Immune cell
Other Intervention Name(s)
InnoLAK
Intervention Description
InnoLak two consecutive weeks every 3 weeks for 3 times
Intervention Type
Radiation
Intervention Name(s)
Low dose radiation
Other Intervention Name(s)
Whole body radiation
Intervention Description
20cGy whole body radiation every three weeks for three times
Primary Outcome Measure Information:
Title
Response rate
Description
Response rate according to RECIST criteria for 12 months
Time Frame
12months
Secondary Outcome Measure Information:
Title
Toxicity
Description
Toxcity according to CTCSEver4.0
Time Frame
12months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients must have signed an approved informed consent and authorization permitting release of personal health information.
Age 18-75 years
Pathologically proven recurrent or persistent cervical cancer patients resistant to conventional palliative chemotherapy or radiation therapy
Persistent tumor more than 1cm after initial chemoradiation or radiation therapy
Persistent tumor more than 1cm after chemoradiation, radiation or chemotherapy in recurrent cervical cancer
Metastatic cervical cancer to lung resistant to conventional chemotherapy
ECOG performance status 0, 1, 2.
Expected survival more than 3 months
Patients must have adequate:
Hematologic function: ANC ≥ 1,500/mcl, Hemoglobin >10g/dL, platelets ≥ 100,000/mcl Renal function: creatinine ≤ 1.5 x ULN Hepatic function: AST, ALT ≤ 1.5 x ULN,
More than 3 weeks from the last day of previous chemotherapy or radiation
Exclusion Criteria:
Patients with immune disease or auto-immune disease (ex. rheumatoid arthritis, SLE, immune vasculitis, IDDM)
Immune deficiency disease
Cancers other than cervical cancer within 5 years
Acute myocardial infarction, uncontrolled hypertension
Severe allergic disease
Severe psychotic disease
Those who can be a candidate for curative surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sang-Young Ryu, MD
Organizational Affiliation
Korea Institute of Radiological & Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sang-Young Ryu
City
Seoul
State/Province
Nowon-Gu
ZIP/Postal Code
139-706
Country
Korea, Republic of
12. IPD Sharing Statement
Learn more about this trial
A Pilot Study of Radiation-Immune Cell Combination Therapy in Cervical Cancer
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