Gefitinib in Treating Patients With Previously Untreated Stage IIIB or Stage IV Non-Small Cell Lung Cancer

Lung Cancer Clinical Trial

Official title:

A Phase II, Open Label Study of Gefitinib (IRESSA) in Treatment-Naïve Subjects With Stage IIIB or IV Non-Small Cell Lung Cancer and Somatic Activating Mutations in the Epidermal Growth Factor Receptor

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00411047
• Other study ID #: 04-291
• Secondary ID: IRUSIRES0483
• Status: Completed
• Phase: Phase 2
• First received: December 11, 2006
• Last updated: May 12, 2013
• Start date: September 2005
• Est. completion date: December 2012

Study information

• Verified date: May 2013
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Gefitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

PURPOSE: This phase II trial is studying how well gefitinib works in treating patients with previously untreated stage IIIB or stage IV non-small cell lung cancer.

Description:

OBJECTIVES:

Primary

• Determine the objective tumor response rate in patients with previously untreated stage IIIB or IV non-small cell lung cancer with somatic activating mutations in the TK region of the epidermal growth factor receptor (EGFR) gene treated with gefitinib.

Secondary

• Determine response duration, progression-free survival, and overall survival of patients treated with this drug.

• Determine the safety of this drug in these patients.

• Compare the ability of various somatic activating mutations in the TK region of the EGFR gene to predict response in patients treated with this drug.

• Compare the ability of various somatic activating mutations in the TK region of the EGFR gene to predict toxicity of this drug in these patients.

• Define a molecular profile in patients who initially respond to treatment with this drug but subsequently progress on therapy.

• Determine the significance of germline polymorphisms of the EGFR gene, somatic amplification of the EGFR gene, and other molecular factors for their association with clinical outcome parameters in these patients.

OUTLINE: This is an open-label study.

Patients receive oral gefitinib once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 2 months.

PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: December 2012
• Est. primary completion date: January 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Pathologically confirmed non-small cell lung cancer (NSCLC)

• No squamous cell histology

• Stage IIIB (with pleural effusion) or stage IV disease

• Must meet = 1 of the following criteria:

• Female

• Adenocarcinoma tumor histology

• No history of smoking, defined as smoking < 100 cigarettes (5 standard packs of cigarettes) in a lifetime, < 20 oz of pipe tobacco in a lifetime, OR < 100 cigars in a lifetime

• Asian/Pacific Rim ethnicity, defined as Japanese, Chinese, Korean, or other Asian/Pacific Rim ethnicity

• Must have activating mutations in the TK region of the epidermal growth factor receptor (EGFR) gene

• Measurable disease

• No symptomatic or newly diagnosed CNS metastases that have not been definitively treated with radiotherapy and/or surgery

• History of CNS metastases or cord compression allowed if definitively treated and clinically stable

PATIENT CHARACTERISTICS:

• See Disease Characteristics

• ECOG performance status 0-2

• Life expectancy = 12 weeks

• Absolute neutrophil count = 2,000/mm³

• Platelet count = 100,000/mm³

• Bilirubin = 1.25 times upper limit of normal (ULN)

• ALT and AST = 2.5 times ULN (5 times ULN if liver has tumor involvement)

• Creatinine = 1.5 times ULN OR creatinine clearance = 60 mL/min

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No known severe hypersensitivity to gefitinib or any other component of gefitinib tablets

• No evidence of clinically active interstitial lung disease

• Patients with chronic, stable radiographic changes who are asymptomatic are eligible

• No other concurrent malignancy or malignancy diagnosed within the past 5 years except for basal cell carcinoma of the skin or cervical cancer in situ

• No concurrent severe or uncontrolled systemic disorder

• No evidence of any other significant clinical disorder or laboratory finding that, in the opinion of the investigator, would preclude study participation

• Able to tolerate protocol treatment, in the opinion of the investigator

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No prior systemic chemotherapy, biological therapy, immunotherapy, or hormonal therapy for NSCLC, including adjuvant and neoadjuvant treatment

• No prior radiotherapy to the target lesion

• Prior radiotherapy to bony disease or CNS disease allowed

• At least 2 weeks since prior radiotherapy and recovered

• More than 30 days since prior non-FDA approved or investigational agents

• No prior EGFR antagonists

• At least 2 weeks since prior and no concurrent phenytoin, carbamazepine, rifampin, barbiturates, or Hypericum perforatum (St. John's wort)

• No concurrent chemotherapy, immunotherapy, hormonal therapy, nonpalliative radiotherapy, surgery for cancer, or other experimental medications

• No other concurrent specific antitumor therapy

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• gefitinib
oral drug taken daily around the same time

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective tumor response rate			No
Secondary	Response duration, progression-free survival, and overall survival			No
Secondary	Safety			Yes
Secondary	Ability of various somatic activating mutations in the TK region of the epidermal growth factor receptor (EGFR) gene to predict response and toxicity			Yes
Secondary	Molecular profile			No
Secondary	Significance of germline polymorphisms of the EGFR gene, somatic amplification of the EGFR gene, and other molecular factors for their association with clinical outcome parameters			No

External Links

•   Clinical trial summary from the National Cancer Institute's PDQ® database