Clinical Trials Directory

Trials / Completed

CompletedNCT00330746

CALC-1 (Cetuximab in Advanced Lung Cancer): Study of 2 Methods of Combining Cetuximab and Gemcitabine in Patients With Advanced Non Small-cell Lung Cancer

Randomized Phase II Study of Cetuximab in Combination With Gemcitabine or Gemcitabine Followed by Cetuximab in Advanced Non Small-cell Lung Cancer Patients Who Are Not Candidates for Platinum Based Therapy.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
National Cancer Institute, Naples · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to select the more promising method of combining cetuximab with gemcitabine for treating patients with advanced non small-cell lung cancer, who are not candidates for platinum based therapy.

Detailed description

The standard treatment for advanced non small cell lung cancer (NSCLC) is combination chemotherapy with cisplatin or carboplatin. Due to its toxicity, this therapy may not be suited for certain patients including the elderly, those whose general condition is poor. Combining chemotherapy with a biologic agent ("targeted therapy") is a new strategy being evaluated for the treatment of NSCLC, and cetuximab is one of the drugs that has shown promise for its activity and tolerability. This study aims to determine the more promising of 2 methods of combining gemcitabine with cetuximab (in combination vs. sequential administration), in two groups of patients who are not candidates for combination platinum based chemotherapy: patients under age 70 with performance status 2 (expected enrollment 42) , and patients over age 70 (expected enrollment 58). Patients will be randomly assigned to one of two treatment arms: * Arm A: Cetuximab + Gemcitabine: * Cetuximab given intravenously weekly AND * Gemcitabine given intravenously for a maximum of 6 cycles (on days 1 and 8 of each 3 week cycle) * Arm B: Gemcitabine followed by Cetuximab: * Gemcitabine given intravenously for a maximum of 6 cycles (on days 1 and 8 of each 3 week cycle) THEN * Cetuximab given intravenously weekly In Arm B, Cetuximab is administered as maintenance therapy when there has been an objective response to chemotherapy, or as second line therapy in patients who had disease progression during chemotherapy

Conditions

Interventions

TypeNameDescription
DRUGcetuximab400 mg/m2 first dose then weekly at 250 mg/m2 until disease progression
DRUGgemcitabine1200 mg/m2 days 1 and 8 every 3 weeks for a maximum of 6 cycles
DRUGgemcitabine1200 mg/m2 IV days 1 and 8 every 3 weeks for a maximum of 6 cycles
DRUGcetuximab400 mg/m2 first dose followed by 250 mg/m2 weekly

Timeline

Start date
2005-11-01
Primary completion
2008-01-01
Completion
2008-06-01
First posted
2006-05-29
Last updated
2012-05-18

Locations

25 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT00330746. Inclusion in this directory is not an endorsement.