Combined Effect of Natural Killer Cell and Doublet Chemotherapy in Advanced NSCLC as the 1st Line Treatment (ANKL-2)
Primary Purpose
Non-small Cell Lung Cancer
Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
ANKL(Ex vivo-expanded NK cell enriched lymphocytes)
Sponsored by
About this trial
This is an interventional treatment trial for Non-small Cell Lung Cancer focused on measuring Autologous Ex vivo-expanded NK cell enriched lymphocytes
Eligibility Criteria
Inclusion Criteria:
- advanced NSCLC with measurable lesions,
- age of 20 - 75 years, Eastern Cooperative Oncology Group (ECOG)
- performance status (PS) of 0 to 2, and stable response after x2 induction chemotherapy as first line treatment.
- No major organ dysfunction.
Exclusion Criteria:
- pregnant or lactating woman,
- active hepatitis B or C,
- AIDS or positivity for HIV, autoimmune diseases or treatment with immunosuppressive drugs,
- prior radiotherapy to the target region
Sites / Locations
- Daejeon St. Mary's HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
ANKL combined with chemotherapy
Arm Description
combination of ANKL and doublet chemotherapy as 3rd and 4th course in patients who get stable response after initial x2 courses
Outcomes
Primary Outcome Measures
response rate
confirmed response rate by CT scan
Secondary Outcome Measures
progression free survival
CT or other imaging modality
Full Information
NCT ID
NCT02370017
First Posted
February 1, 2015
Last Updated
February 1, 2017
Sponsor
The Catholic University of Korea
1. Study Identification
Unique Protocol Identification Number
NCT02370017
Brief Title
Combined Effect of Natural Killer Cell and Doublet Chemotherapy in Advanced NSCLC as the 1st Line Treatment
Acronym
ANKL-2
Official Title
Combined Effect of Autologous Ex-vivo Expanded Activated NK Cell-lymphocytes (ANKL) and Doublet Chemotherapy in Patients With Advanced NSCLC as the 1st Line Treatment; Phase II
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
August 2018 (Anticipated)
Study Completion Date
February 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Catholic University of Korea
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The object of this study is to identify the combined effect of ANKL and doublet chemotherapy in advanced NSCLC. The investigators design the combination of ANKL and approved chemotherapy as the 3rd and 4th courses in the patients who get stable response after x2 induction as the first line chemotherapy. ANKL (2x10*9) from peripheral blood 32ml is administered rapidly iv 12-36hr after each chemotherapeutic agents while peak effect of NK cell ligand modulation by chemotherapeutic agent is maintained. After 4th course, response evaluation is done by Response Evaluation Criteria in Solid Tumors (RECIST) and 40% or more partial response (PR, increased by 15% or more from historical control 25%) is the expected target and Simon's two stage design will be applied through the study (power 80%, a= 0.95, N1= 33, N= 68)
Detailed Description
Based on additive or synergistic effect of natural killer (NK) cell and chemotherapy (modulating the expression of NK stimulatory ligand on tumor cell), the investigators performed phase II trial of docetaxel and ANKL combination s the second line treatment in advanced non-small cell lung cancer (NSCLN) and reported the results in May 2013. (Anticancer Research 33;2115, Poster Presentation in ASCO).In that study, the investigators observed the feasibility and safety of ANKL combined with docetaxel in patients with advanced NSCLC, but the clinical benefit was not evaluated properly because the study was interrupted unintentionally and most of the enrolled patients were far advanced with large tumor burden, that is, poor immunological environment for ANKL to work.
The object of this study is to identify the combined effect of ANKL and doublet chemotherapy in advanced NSCLC. The approved doublet chemotherapy based on platinum is widely used with the response rate (RR) 25-35% after 4-6 courses as the first line treatment. The investigators design the combination of ANKL and chemotherapy as the 3rd and 4th courses in the patients who show stable response after x2 courses. Higher RR with the combination treatment is the primary outcome as compared with the chemotherapy alone - historical control; about 12% PR and 50% stable response after x2 initial courses and 25% PR after x2 more courses among the patients who get stable response after x2 initial courses. Peripheral blood 32 ml will be drawn from the patients who decide to be enrolled and about 2 weeks later ANKL (2x10*9) are scheduled to be administered rapidly iv 12-36hr after each chemotherapeutic agents while peak effect of NK cell ligand modulation by chemotherapeutic agent is maintained. After 4th course, response evaluation is done by RECIST and 40% or more PR (increased by 15% or more from historical control 25%) is the expected target and Simon's two stage design will be applied through the study (power 80%, a= 0.95, N1= 33, N= 68)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-small Cell Lung Cancer
Keywords
Autologous Ex vivo-expanded NK cell enriched lymphocytes
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
68 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
ANKL combined with chemotherapy
Arm Type
Experimental
Arm Description
combination of ANKL and doublet chemotherapy as 3rd and 4th course in patients who get stable response after initial x2 courses
Intervention Type
Biological
Intervention Name(s)
ANKL(Ex vivo-expanded NK cell enriched lymphocytes)
Intervention Description
add ANKL in 3rd and 4th course in case of stable response after two initial courses
Primary Outcome Measure Information:
Title
response rate
Description
confirmed response rate by CT scan
Time Frame
1 month later after 4th course
Secondary Outcome Measure Information:
Title
progression free survival
Description
CT or other imaging modality
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
advanced NSCLC with measurable lesions,
age of 20 - 75 years, Eastern Cooperative Oncology Group (ECOG)
performance status (PS) of 0 to 2, and stable response after x2 induction chemotherapy as first line treatment.
No major organ dysfunction.
Exclusion Criteria:
pregnant or lactating woman,
active hepatitis B or C,
AIDS or positivity for HIV, autoimmune diseases or treatment with immunosuppressive drugs,
prior radiotherapy to the target region
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bo Ra Hong, RN
Phone
+82-10-6402-9535
Email
shbrp@hanmail.net
First Name & Middle Initial & Last Name or Official Title & Degree
Young Jun Yang, MD
Phone
+82-10-6435-7009
Email
yyj7009@hanmail.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Suk Young Park, MD, PhD
Organizational Affiliation
The Catholic University of Korea
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hoon Kim, MD, PhD
Organizational Affiliation
The Catholic University of Korea
Official's Role
Study Director
Facility Information:
Facility Name
Daejeon St. Mary's Hospital
City
Jung-gu
State/Province
Daejeon
ZIP/Postal Code
34943
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Suk Young Park, MD, PhD
Phone
82-42-220-9821
Email
sypark1011@hotmail.com
First Name & Middle Initial & Last Name & Degree
young Jun Yang, MD
Phone
82-10-6435-7009
Email
yyj7009@daum.net
12. IPD Sharing Statement
Learn more about this trial
Combined Effect of Natural Killer Cell and Doublet Chemotherapy in Advanced NSCLC as the 1st Line Treatment
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