Phase 1 Clinical Trial to Evaluate the Safety of Allogeneic NK Cell ("SMT-NK") Cell Therapy in Advanced Biliary Tract Cancer
Primary Purpose
Advanced Biliary Tract Cancer
Status
Completed
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Natural killer cell
Sponsored by
About this trial
This is an interventional treatment trial for Advanced Biliary Tract Cancer
Eligibility Criteria
Inclusion Criteria:
- patients with pathologically proven biliary tract cancer (gallbladder cancer, cholangiocarcinoma),
- patients with refractory disease after chemotherapy and/or patients who have difficulty with chemotherapy due to side effects of chemotherapy
- 18y≤age≤75y
- ECOG performance status (ECOG-PS) ≤2
- Patients who meet the following conditions; 1)ANC ≥ 1,500/μL, 2) Hemoglobin) ≥ 10 g/dL, 3) PLT > 100,000/ μL, 4) Serum BUN & Creatinine ≤ 1.5 x ULN, 5) AST & ALT ≤ 2.5 x ULN, 6) Bilirubin ≤ 3mg/L
- Informed consent
Exclusion Criteria:
- Immune deficiency or autoimmune disease that can be exacerbated by immunotherapy
- Pregnancy
- Patients who have a history of other malignancies except skin cancer, local prostate cancer or cervical intraepithelial neoplasm within 5 years before the start of this study
- Serious allergic history, psychological disease
- Breast feeding or Patients planning pregnancy
Sites / Locations
- Division of Gastroenterology, Department of Internal Medicine, Yonsei University College of Medicine
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
experimental group
Arm Description
Outcomes
Primary Outcome Measures
Dose limiting toxicity
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Dose limiting toxicity
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Dose limiting toxicity
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Dose limiting toxicity
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Maximum Tolerated Dose
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Maximum Tolerated Dose
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Maximum Tolerated Dose
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Maximum Tolerated Dose
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03358849
Brief Title
Phase 1 Clinical Trial to Evaluate the Safety of Allogeneic NK Cell ("SMT-NK") Cell Therapy in Advanced Biliary Tract Cancer
Official Title
Phase 1 Clinical Trial to Evaluate the Safety of Allogeneic NK Cell ("SMT-NK") Cell Therapy in Advanced Biliary Tract Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
October 17, 2017 (Actual)
Primary Completion Date
September 27, 2018 (Actual)
Study Completion Date
September 27, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Cholangiocarcinoma refers to bile duct cancer (bile duct cancer) and gallbladder cancer that develop in the gallbladder. According to the data from National Cancer Information Center in 2013, the incidence of cancer in Korea is 5,283, which corresponds to about 2.3% of all cancers and the 5-year survival rate is 30% And most of the long-term survival is due to early detection by screening, and advanced carcinoma is a refractory carcinoma with a 5-year survival rate of less than 5%. In addition to the standard anticancer drugs, alternative anticancer drugs and targeted therapies have been developed to provide a variety of treatment modalities. However, the development of cell therapy drugs for cancer, such as cancers, has not been developed in Korea. .
Natural killer cells (NK cells) are innate lymphocyte cells with cytotoxic activity. Unlike T cells and B cells, which have antigen-specific receptors, NK cells express various innate immunoreceptors on the cell surface, thereby enabling selective recognition of cancer cells And recognizes cancer cells, it is a cytotoxic cell that can immediately remove cancer cells without any other activation process. In addition, natural killer cells also interact with dendritic cells or T cells directly or indirectly to regulate the immune response, thereby inhibiting the development and metastasis of cancer cells and effectively removing cancer stem cells important for cancer recurrence It has many advantages in the development of anti-cancer immunotherapy.
Detailed Description
Cholangiocarcinoma refers to bile duct cancer (bile duct cancer) and gallbladder cancer that develop in the gallbladder. According to the data from National Cancer Information Center in 2013, the incidence of cancer in Korea is 5,283, which corresponds to about 2.3% of all cancers and the 5-year survival rate is 30% And most of the long-term survival is due to early detection by screening, and advanced carcinoma is a refractory carcinoma with a 5-year survival rate of less than 5%. In addition to the standard anticancer drugs, alternative anticancer drugs and targeted therapies have been developed to provide a variety of treatment modalities. However, the development of cell therapy drugs for cancer, such as cancers, has not been developed in Korea. .
Although surgical resection is mandatory for curettage of the biliary tract, 40 ~ 50% of all patients are able to undergo radical resection. In general, the incidence of mid / lower bile duct cancer is high and the upper bile duct cancer is relatively low. The surgical resection of the tumor depends on the location of the tumor. The curative surgery of the biliary cancer is very complicated and time-consuming. The anatomical structures of the biliary and vascular system are variable and it is difficult to accurately determine the extent of the tumor invasion before surgery or even during surgery there is also a great deal of risk. Especially in the case of hepatic portal biliary duct (upper bile duct cancer), it is difficult to judge whether surgical resection is feasible, and there are many cases where resection is difficult at the time of operation or discovery. Gallbladder cancer also has a poor prognosis. Early cancer can be cured by surgery, but progressive cancer has a poor prognosis and overall survival rate is similar to that of biliary cancer. Because it occurs in the biliary tract with bile duct cancer, the clinical method and characteristics of the cancer cells are similar, and the same method is used for the treatment and the chemotherapy.
However, since there is no standard for the selection of second-line chemotherapy after gemcitabine treatment, the development of an alternative therapeutic agent is urgently required have.
Natural killer cells (NK cells) are innate lymphocyte cells with cytotoxic activity. Unlike T cells and B cells, which have antigen-specific receptors, NK cells express various innate immunoreceptors on the cell surface, thereby enabling selective recognition of cancer cells And recognizes cancer cells, it is a cytotoxic cell that can immediately remove cancer cells without any other activation process. In addition, natural killer cells also interact with dendritic cells or T cells directly or indirectly to regulate the immune response, thereby inhibiting the development and metastasis of cancer cells and effectively removing cancer stem cells important for cancer recurrence It has many advantages in the development of anti-cancer immunotherapy.
Therefore, various clinical studies have been conducted to treat cancer using natural killer cells worldwide, including in Korea, and therapeutic clinical results are shown for various cancers. The clinical application of natural killer cells is carried out by culturing natural killer cells isolated from blood of patient, patient's family or even from other people's blood and injecting them into patients. It is also possible to expect the effect as a combination therapy with chemotherapy alone or by eliminating the cancer cells in the patient's body while improving the immunity of the patient by improving the immunity of the patient.
However, despite this, the clinical application of natural killer cells in Korea is limited to only a few cancers, including hematologic and hepatocellular carcinoma.
Carcinoid cancer (biliary cancer, gallbladder cancer) is a rare carcinoma with around 3,500 cases per year in Korea. In the majority of cases, the rate of relying entirely on chemotherapy is more than 50%, and the response rate of Gemcitabine based on the first chemotherapy is about 30%. Other alternative therapies that do not lead to cancer are natural killer cells that need to be tested for safety and efficacy in existing drugs.
In Korea, the clinical application of natural killer cells is limited to only a few cancers, including hematologic and hepatocellular carcinomas. Carcinoid cancer (biliary cancer, gallbladder cancer) is a rare carcinoma with around 3,500 cases per year in Korea. In the majority of cases, the rate of relying entirely on chemotherapy is more than 50%, and the response rate of Gemcitabine based on the first chemotherapy is about 30%. Other alternative therapies that do not lead to cancer are natural killer cells that need to be tested for safety and efficacy in existing drugs.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Biliary Tract Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
experimental group
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Natural killer cell
Other Intervention Name(s)
SMT-NK cell
Intervention Description
Patients who received natural killer cell injection
Primary Outcome Measure Information:
Title
Dose limiting toxicity
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
1 week after NK cell injection
Title
Dose limiting toxicity
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
2 weeks after NK cell injection
Title
Dose limiting toxicity
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
3 weeks after NK cell injection
Title
Dose limiting toxicity
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
4 weeks after NK cell injection
Title
Maximum Tolerated Dose
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
1 week after NK cell injection
Title
Maximum Tolerated Dose
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
2 weeks after NK cell injection
Title
Maximum Tolerated Dose
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
3 weeks after NK cell injection
Title
Maximum Tolerated Dose
Description
Adverse event and drug related toxicity will be checked every week by the investigator's monitoring.
Time Frame
4 weeks after NK cell injection
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
patients with pathologically proven biliary tract cancer (gallbladder cancer, cholangiocarcinoma),
patients with refractory disease after chemotherapy and/or patients who have difficulty with chemotherapy due to side effects of chemotherapy
18y≤age≤75y
ECOG performance status (ECOG-PS) ≤2
Patients who meet the following conditions; 1)ANC ≥ 1,500/μL, 2) Hemoglobin) ≥ 10 g/dL, 3) PLT > 100,000/ μL, 4) Serum BUN & Creatinine ≤ 1.5 x ULN, 5) AST & ALT ≤ 2.5 x ULN, 6) Bilirubin ≤ 3mg/L
Informed consent
Exclusion Criteria:
Immune deficiency or autoimmune disease that can be exacerbated by immunotherapy
Pregnancy
Patients who have a history of other malignancies except skin cancer, local prostate cancer or cervical intraepithelial neoplasm within 5 years before the start of this study
Serious allergic history, psychological disease
Breast feeding or Patients planning pregnancy
Facility Information:
Facility Name
Division of Gastroenterology, Department of Internal Medicine, Yonsei University College of Medicine
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Phase 1 Clinical Trial to Evaluate the Safety of Allogeneic NK Cell ("SMT-NK") Cell Therapy in Advanced Biliary Tract Cancer
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