Gemcitabine and Carboplatin for Elderly Patient With Lung Cancer (GEEP)
Primary Purpose
Non-Small Cell Lung Cancer
Status
Completed
Phase
Phase 2
Locations
Japan
Study Type
Interventional
Intervention
gemcitabine and carboplatin
Gemcitabine
Sponsored by

About this trial
This is an interventional treatment trial for Non-Small Cell Lung Cancer focused on measuring Elder Patients, Non-Small Cell Lung Cancer, Previously Untreated, Advanced
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of histologically confirmed stage IIIB or IV non-small cell lung cancer
- Good performance status (ECOG 0-1)
- No previous treatment
- Age 76 years and older
- Adequate bone marrow, liver and renal functions
- No pregnant
- Measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >=1.0 cm by spiral CT scan
- Provided written informed consent
Exclusion Criteria:
- Severe complications or a concomitant malignancy
- Prior and other concurrent radiotherapy, chemotherapy, immunotherapy, EGFR tyrosine kinase inhibitors
- Interstitial pneumonia or lung fibrosis
- Contraindicated gemcitabine or carboplatin
- Inappropriate patients for entry to this study, judged by the physicians
Sites / Locations
- Hamamatsu University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
Gemcitabine 1000mg/m2 Day 1,15 Carboplatin AUC=3 Day 1, 15 every 4 weeks
Gemcitabine 1000mg/m2 Day 1, 8, 15
Outcomes
Primary Outcome Measures
Efficacy (response rate)
Secondary Outcome Measures
The toxicity profile (adverse event profile)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00881296
Brief Title
Gemcitabine and Carboplatin for Elderly Patient With Lung Cancer
Acronym
GEEP
Official Title
Randomized Phase II Study of Biweekly Chemotherapy With Gemcitabine and Carboplatin in Elder Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2010
Overall Recruitment Status
Completed
Study Start Date
March 2008 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hamamatsu University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A comparison of biweekly combination chemotherapy (gemcitabine plus carboplatin) with weekly gemcitabine in elder patients (> 75) with previously untreated advanced non-small cell lung cancer. Primary objective is to determine the objective response rate (CR+PR by RECIST criteria) for biweekly gemcitabine and carboplatin combination chemotherapy versus weekly single gemcitabine as first-line therapy in elder advanced non-small lung cancer patients (> 76 years) who have received no prior treatment for non-small lung cancer. As secondary objectives, adverse event profile, tolerability of biweekly gemcitabine and carboplatin combination chemotherapy, progression-free survival and overall survival will be evaluated in both patients with biweekly gemcitabine and carboplatin combination chemotherapy and weekly single gemcitabine.
The study hypothesis is that biweekly combination chemotherapy of gemcitabine plus carboplatin may improve the efficacy.
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
Elder Patients, Non-Small Cell Lung Cancer, Previously Untreated, Advanced
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Gemcitabine 1000mg/m2 Day 1,15
Carboplatin AUC=3 Day 1, 15 every 4 weeks
Arm Title
2
Arm Type
Active Comparator
Arm Description
Gemcitabine 1000mg/m2 Day 1, 8, 15
Intervention Type
Drug
Intervention Name(s)
gemcitabine and carboplatin
Intervention Description
Gemcitabine 1000mg/m2, DIV on day 1 and 15 of each 28 day cycle. Carboplatin AUC=3, DIV on day 1 and 15 of each 28 day cycle. Number of cycles: until progression or unacceptable toxicity develops, up to 6 cycles.
Intervention Type
Drug
Intervention Name(s)
Gemcitabine
Intervention Description
Gemcitabine 1000mg/m2, DIV on day 1, 8 and 15 of each 28 day cycle. Number of cycles: until progression or unacceptable toxicity develops, up to 6 cycles
Primary Outcome Measure Information:
Title
Efficacy (response rate)
Time Frame
two-years, followed RECIST criteria
Secondary Outcome Measure Information:
Title
The toxicity profile (adverse event profile)
Time Frame
two-years, followed NCI-CTCAE criteria
10. Eligibility
Sex
All
Minimum Age & Unit of Time
76 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of histologically confirmed stage IIIB or IV non-small cell lung cancer
Good performance status (ECOG 0-1)
No previous treatment
Age 76 years and older
Adequate bone marrow, liver and renal functions
No pregnant
Measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >=1.0 cm by spiral CT scan
Provided written informed consent
Exclusion Criteria:
Severe complications or a concomitant malignancy
Prior and other concurrent radiotherapy, chemotherapy, immunotherapy, EGFR tyrosine kinase inhibitors
Interstitial pneumonia or lung fibrosis
Contraindicated gemcitabine or carboplatin
Inappropriate patients for entry to this study, judged by the physicians
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kingo Chida, MD,PhD
Organizational Affiliation
Hamamatsu University
Official's Role
Study Chair
Facility Information:
Facility Name
Hamamatsu University School of Medicine
City
Hamamatsu
State/Province
Shizuoka
ZIP/Postal Code
431-3192
Country
Japan
12. IPD Sharing Statement
Citations:
PubMed Identifier
22705118
Citation
Kusagaya H, Inui N, Karayama M, Nakamura Y, Kuroishi S, Yokomura K, Toyoshima M, Shirai T, Masuda M, Yamada T, Yasuda K, Suda T, Chida K. Biweekly combination therapy with gemcitabine and carboplatin compared with gemcitabine monotherapy in elderly patients with advanced non-small-cell lung cancer: a randomized, phase-II study. Lung Cancer. 2012 Sep;77(3):550-5. doi: 10.1016/j.lungcan.2012.05.106. Epub 2012 Jun 15.
Results Reference
derived
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Gemcitabine and Carboplatin for Elderly Patient With Lung Cancer
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