Working… Menu
Trial record 76 of 543 for:    Celecoxib

Gefitinib and Celecoxib in Treating Patients With Refractory Non-Small Cell Lung Cancer

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00068653
Recruitment Status : Completed
First Posted : September 11, 2003
Last Update Posted : April 29, 2013
National Cancer Institute (NCI)
Information provided by (Responsible Party):
Barbara Ann Karmanos Cancer Institute

Brief Summary:

RATIONALE: Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Celecoxib may slow the growth of cancer by stopping blood flow to the tumor. Combining gefitinib with celecoxib may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of combining gefitinib with celecoxib in treating patients who have non-small cell lung cancer that is refractory to platinum-based chemotherapy (such as cisplatin or carboplatin).

Condition or disease Intervention/treatment Phase
Lung Cancer Drug: Celecoxib Drug: ZD1839 Phase 2

Detailed Description:



  • Determine the response rate in patients with platinum-refractory non-small cell lung cancer treated with gefitinib and celecoxib.


  • Determine the progression-free and overall survival of patients treated with this regimen.
  • Determine the toxicity of this regimen in these patients.

OUTLINE: Patients receive oral gefitinib once daily and oral celecoxib twice daily on days 1-28. Treatment repeats every 28 days for up to 3 courses in the absence of disease progression or unacceptable toxicity.

Patients are followed for up to 6 weeks.

PROJECTED ACCRUAL: A total of 18-27 patients will be accrued for this study within 22 months.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 27 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase II Study of the Combination of ZD1839 (Iressa) and Celecoxib in Patients With Platinum Refractory Non-Small Cell Lung Cance
Study Start Date : June 2003
Actual Primary Completion Date : October 2007
Actual Study Completion Date : May 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Lung Cancer

Arm Intervention/treatment
Experimental: Celecoxib & ZD1839

Celecoxib: 400mg orally two times a day, taken with meals.

ZD1839: 250 mg po every day, taken with or without food.

Drug: Celecoxib
Celecoxib 400mg orally two times a day, taken with meals.
Other Name: Celebrex

Drug: ZD1839
ZD1839 250 mg po every day, taken with or without food.
Other Names:
  • Iressa
  • Gefitinib

Primary Outcome Measures :
  1. Response rate [ Time Frame: Every 2 cycles; after the 1st 4 cycles, every month by clinical exam & every 3 months radiological evaluation ]
    CT scan chest/abdomen; Assessments of complete response (CR) or partial response (PR)require confirmation 4 weeks or later.

Secondary Outcome Measures :
  1. Progression-free survival (PFS) [ Time Frame: Every 2 cycles; after the 1st 4 cycles, every month by clinical exam & every 3 months radiological evaluation ]
  2. Overall survival [ Time Frame: Every 2 cycles; after the 1st 4 cycles, every month by clinical exam & every 3 months radiological evaluation ]
  3. Toxicity of this drug combination [ Time Frame: Every 2 weeks; Every month after 4 cycles if the patient has not developed > Grade 2 toxicity ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No


  • Histologically or cytologically confirmed non-small cell lung cancer (NSCLC)
  • Progression of disease during platinum-based (cisplatin or carboplatin) chemotherapy or within 3 months of completing chemotherapy

    • Treatment with other agents since prior platinum-based chemotherapy allowed
  • Measurable disease

    • Target lesions within a prior radiation field must have documented evidence of progression at least 8 weeks after the completion of radiotherapy
  • No active brain or leptomeningeal metastases

    • Treated brain metastases allowed at least 4 weeks after the completion of appropriate therapy



  • 18 and over

Performance status

  • ECOG 0-2

Life expectancy

  • Not specified


  • Absolute neutrophil count at least 1,500/mm^3
  • Platelet count at least 100,000/mm^3
  • Hemoglobin at least 8 g/dL


  • Bilirubin no greater than upper limit of normal (ULN)
  • AST/ALT no greater than 2.5 times ULN (if alkaline phosphatase is no greater than ULN)
  • Alkaline phosphatase no greater than 5 times ULN (if AST and ALT are greater than ULN)
  • No history of chronic hepatitis


  • Creatinine no greater than 1.5 times ULN


  • No active thromboembolic event within the past 4 weeks
  • No uncontrolled congestive heart failure
  • No uncontrolled angina
  • No myocardial infarction and/or stroke within the past 6 months


  • No evidence of clinically active interstitial lung disease


  • No history of gastrointestinal bleeding within the past 6 months
  • No history of peptic ulcer disease


  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Must weigh at least 110 pounds (50 kg)
  • HIV negative
  • No allergy to sulfonamides
  • No allergy to any NSAID, including celecoxib
  • No known severe hypersensitivity to gefitinib or any of its excipients
  • No other malignancy within the past 3 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix
  • No history of dementia, active psychiatric disorder, or any other condition that would preclude study compliance
  • No other concurrent serious medical condition


Biologic therapy

  • No prior epidermal growth factor receptor inhibitor
  • No concurrent biologic therapy


  • See Disease Characteristics
  • More than 2 weeks since prior chemotherapy

Endocrine therapy

  • Not specified


  • Recovered from prior radiotherapy


  • Recovered from prior surgery


  • Recovered from prior therapy
  • More than 2 weeks since prior investigational therapy
  • More than 1 week since prior fluconazole
  • More than 30 days since prior participation in another investigational agent clinical trial
  • More than 30 days since prior chronic nonsteroidal anti-inflammatory drugs (NSAIDs), including celecoxib or rofecoxib
  • No prior gefitinib
  • No prior cyclooxygenase-2 (COX-2) inhibitor or another clinical trial for NSCLC
  • No other concurrent NSAIDs

    • Concurrent aspirin allowed (not to exceed 325 mg/day)
  • No other concurrent COX-2 inhibitors
  • No concurrent lithium
  • No concurrent fluconazole
  • No concurrent use of any of the following:

    • Phenytoin
    • Carbamazepine
    • Barbiturates
    • Rifampin
    • Phenobarbital
    • Hypericum perforatum

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00068653

Layout table for location information
United States, Michigan
Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States, 48201-1379
Sponsors and Collaborators
Barbara Ann Karmanos Cancer Institute
National Cancer Institute (NCI)
Layout table for investigator information
Study Chair: Shirish M. Gadgeel, MD Barbara Ann Karmanos Cancer Institute

Layout table for additonal information
Responsible Party: Barbara Ann Karmanos Cancer Institute Identifier: NCT00068653     History of Changes
Other Study ID Numbers: CDR0000327805
P30CA022453 ( U.S. NIH Grant/Contract )
First Posted: September 11, 2003    Key Record Dates
Last Update Posted: April 29, 2013
Last Verified: April 2013
Keywords provided by Barbara Ann Karmanos Cancer Institute:
recurrent non-small cell lung cancer
Additional relevant MeSH terms:
Layout table for MeSH terms
Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Inflammatory Agents
Antirheumatic Agents
Cyclooxygenase 2 Inhibitors
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Protein Kinase Inhibitors