search
Back to results

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
Hamamatsu University
About
Eligibility
Locations
Arms
Outcomes
Full info

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

76 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
April 14, 2009
Last Updated
September 5, 2011
Sponsor
Hamamatsu University
search

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

Learn more about this trial

Gemcitabine and Carboplatin for Elderly Patient With Lung Cancer

We'll reach out to this number within 24 hrs