Trial of Docetaxel Versus Vinorelbine as 1st Line Treatment in Elderly Patients With Non-Small-Cell Lung Cancer (NSCLC)
This study has been completed.
Sponsor:
Hellenic Oncology Research Group
Collaborator:
University Hospital of Crete
Information provided by:
Hellenic Oncology Research Group
ClinicalTrials.gov Identifier:
NCT00441922
First received: February 28, 2007
Last updated: October 28, 2008
Last verified: October 2008
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Purpose
This trial will compare the efficacy of docetaxel versus vinorelbine as first-line treatment in elderly patients with advanced NSCLC.
| Condition | Intervention | Phase |
|---|---|---|
|
Non Small Cell Lung Cancer |
Drug: Docetaxel Drug: Vinorelbine |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Multicenter Randomized Phase II Study of Docetaxel Versus Vinorelbine as First-Line Treatment in Elderly Patients With Advanced Non-Small-Cell Lung Cancer (NSCLC) |
Resource links provided by NLM:
Further study details as provided by Hellenic Oncology Research Group:
Primary Outcome Measures:
- Overall survival between the two treatment arms [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Time to disease progression [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- Toxicity profile [ Time Frame: During the time of chemotherapy ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 166 |
| Study Start Date: | January 2003 |
| Study Completion Date: | January 2008 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
D
|
Drug: Docetaxel
Docetaxel at the dose of 38 mg/m2 IV on days 1 and 8 every 3 weeks for 6 consecutive cycles
Other Name: Taxotere
|
|
Experimental: 2
V
|
Drug: Vinorelbine
Vinorelbine at the dose of 25 mg/m2 IV on days 1 and 8 every 3 weeks for 6 consecutive cycles
Other Name: Navelbine
|
Detailed Description:
Docetaxel and vinorelbine are well known active agents in the treatment of NSCLC. The standard treatment of elderly patients with advanced NSCLC is monotherapy with a third generation agent. The role of comprehensive geriatric assessment in treatment efficacy and tolerance is an area of investigation.
Eligibility| Ages Eligible for Study: | 65 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Histologically- or cytologically- confirmed Non-Small-Cell Lung Cancer
- Stage IIIB/IV
- No prior chemotherapy
- Existence of two-dimensional measurable disease. The measurable disease should not have been irradiated
- Life expectancy of more than 3 months
- Age ≥ 65 years
- Performance status (WHO) ≤ 3
- Adequate bone marrow function (absolute neutrophil count > 1000/mm^3, platelet count > 100000/mm^3, Hemoglobin > 9 gr/mm^3)
- Adequate liver (bilirubin < 1.5 times upper limit of normal and SGOT/SGPT < 2 times upper limit of normal), and renal function (creatinine < 2 mg/dl)
- Informed consent
Exclusion Criteria:
- Psychiatric illness or social situation that would preclude study compliance.
- Other concurrent uncontrolled illness
- Other invasive malignancy within the past 5 years except nonmelanoma skin cancer
- No absence or irradiated and stable central nervous system metastatic disease.
- No presence of a reliable care giver
- Other concurrent investigational agents
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00441922
Locations
| Greece | |
| University General Hospital of Alexandroupolis, Department of Medical Oncology | |
| Alexandroupolis, Greece | |
| Sotiria General Hospital, 1st, 3rd, 8th Department of Pulmonary Diseases | |
| Athens, Greece | |
| IASO General Hospital of Athens, 1st Department of Medical Oncology | |
| Athens, Greece | |
| Laikon General Hospital, Medical Oncology Unit, Propedeutic Department of Internal Medicine | |
| Athens, Greece | |
| Air Forces Military Hospital of Athens | |
| Athens, Greece | |
| Sismanogleio General Hospital, 1st, 2nd Department of Pulmonary Diseases | |
| Athens, Greece | |
| 401 Military Hospital of Athens | |
| Athens, Greece | |
| State General Hospital of Larissa, Department of Medical Oncology | |
| Larissa, Greece | |
| Metaxa's Anticancer Hospital of Piraeus, 1st Department of Medical Oncology | |
| Piraeus, Greece | |
| Theagenion Anticancer Hospital of Thessaloniki | |
| Thessaloniki, Greece | |
Sponsors and Collaborators
Hellenic Oncology Research Group
University Hospital of Crete
Investigators
| Principal Investigator: | Lampros Vamvakas, MD | University Hospital of Crete, Department of Medical Oncology |
More Information
No publications provided
| Responsible Party: | L.Vamvakas, Hellenic Oncology Research Group |
| ClinicalTrials.gov Identifier: | NCT00441922 History of Changes |
| Other Study ID Numbers: | CT/03.07 |
| Study First Received: | February 28, 2007 |
| Last Updated: | October 28, 2008 |
| Health Authority: | Greece: National Organization of Medicines |
Keywords provided by Hellenic Oncology Research Group:
|
Cancer Elderly Chemotherapy Docetaxel Vinorelbine |
Additional relevant MeSH terms:
|
Carcinoma, Non-Small-Cell Lung Lung Neoplasms Carcinoma, Bronchogenic Bronchial Neoplasms Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site Neoplasms Lung Diseases Respiratory Tract Diseases Vinorelbine |
Vinblastine Docetaxel Antineoplastic Agents, Phytogenic Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Tubulin Modulators Antimitotic Agents Mitosis Modulators Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 16, 2013