Erlotinib With or Without Fulvestrant in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

NCT ID: NCT00100854

Last Updated: 2019-03-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 108 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-10-28
• Study Completion Date: 2018-09-05

Brief Summary

RATIONALE: Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Estrogen can cause the growth of non-small cell lung cancer cells. Hormone therapy using fulvestrant may fight non-small cell lung cancer by lowering the amount of estrogen the body makes. Giving erlotinib together with fulvestrant may kill more tumor cells. It is not yet known whether giving erlotinib together with fulvestrant is more effective than erlotinib alone in treating non-small cell lung cancer.

PURPOSE: This randomized phase II trial is studying giving erlotinib together with fulvestrant to see how well it works compared to erlotinib alone in treating patients with stage IIIB or stage IV non-small cell lung cancer.

Detailed Description

OBJECTIVES:

Primary

• Compare objective tumor response in patients stage IIIB or IV non-small cell lung cancer treated with erlotinib hydrochloride with vs without fulvestrant.

Secondary

• Correlate response rate with ER and EGF receptor expression in patients treated with these regimens.
• Correlate measurement of ER-α, ER-β, EGF/HER-1 receptor and HER-2/neu receptor with clinical response in patients treated with these regimens.
• Correlate erlotinib hydrochloride resistance with ER and HER receptor expression in patients treated with these regimens.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to performance status, gender, and participating center. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oral erlotinib hydrochloride once daily on days 1-28. Courses repeat every 28 days.
• Arm II: Patients receive erlotinib hydrochloride as in arm I and fulvestrant intramuscularly on days 1, 15, and 29, and then every 28 days thereafter.

In both arms, treatment continues in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed for 30 days and then every 2 months until disease progression.

PROJECTED ACCRUAL: A total of 102 patients (34 in arm I and 68 in arm II) will be accrued for this study.

Conditions

Lung Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive oral erlotinib hydrochloride once daily on days 1-28. Courses repeat every 28 days.

Group Type: ACTIVE_COMPARATOR

erlotinib hydrochloride

Intervention Type: DRUG

Given orally

Arm II

Patients receive erlotinib hydrochloride as in arm I and fulvestrant intramuscularly on days 1, 15, and 29, and then every 28 days thereafter.

Group Type: EXPERIMENTAL

erlotinib hydrochloride

Intervention Type: DRUG

Given orally

fulvestrant

Intervention Type: DRUG

Given intramuscularly

Interventions

erlotinib hydrochloride

Given orally

Intervention Type: DRUG

fulvestrant

Given intramuscularly

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• adults over the age of 18 capable of giving informed consent.
• Histologically confirmed non-small cell lung cancer
• Stage IIIB or IV NSCLC
• Tumor tissue block available.
• ECOG performance status of 0, 1 or 2.
• Measurable disease by RECIST criteria defined as ≥ 1 target lesion that has not been irradiated. New lesions that have developed in a previously irradiated field may be used as sites of measurable disease provided all other criteria are met.
• Meets 1 of the following criteria:
• Progressive disease after ≥ 1 prior standard chemotherapy regimen
• Refused chemotherapy
• Unable to receive standard chemotherapy
• women of childbearing age must have negative pregnancy test by urine or serum prior to initiation of treatment. men and women of childbearing potential must consent to using adequate contraception throughout treatment and for 3 months following surgery.

Exclusion Criteria

• Renal insufficiency (serum creatinine >2mg/dl)
• Liver insufficiency (serum total bilirubin >1.5X ULN, or serum transaminases > 2.5X the ULN or %X ULN if hepatic metastases).
• hematologic abnormality platelets< 100,000 ANC <1,500/mm3
• THerapeutic anticoagulation will be allowed, but patients receiving fulvestrant while on therapeutic anticoagulation will have the fulvestrant dose divided into twice as many syringes to minimize the volume of intramuscular injection in these patients. In patients receiving low molecular weight heparin or fondaparinux, these medications should be held for 12 hours before and after fulvestrant injection if possible.
• Active CNS metastases.
• New York Heart Association class III or IV cardiac disease
• myocardial infarction within the past 12 months
• symptomatic ventricular arrhythmia
• symptomatic conduction abnormality
• evidence of clinically active interstitial lung disease
• Patients with asymptomatic chronic stable radiographic changes are eligible
• pregnant or nursing or inadequate contraception
• hypersensitivity to erlotinib hydrochloride or fulvestrant or to any of their excipients
• comorbid disease or medical condition that would preclude study treatment or compliance
• malignancy within the past 3 years except nonmelanoma skin cancer or carcinoma in situ of the cervix
• chemotherapy or non-cytotoxic investigational agents within 4 weeks of initiating treatment.
• major surgery within 4 weeks of initiating therapy. Minor surgery within 7 days of initiating therapy.
• anticancer antiestrogen therapy. Concurrent stable-dose steroids allowed
• concomitant radiation therapy to the lungs. Radiation therapy to non-target lesions will be allowed as long as it is completed 1 week prior to initiation of treatment.
• prior anticancer epidermal growth factor receptor inhibitors
• concurrent CYP3A4 inducers, including any of the following:
• Phenytoin
• Carbamazepine
• Rifampin
• Barbiturates
• Hypericum perforatum (St. John's wort)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Translational Oncology Research International

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Edward Garon, MD

Role: PRINCIPAL_INVESTIGATOR

Jonsson Comprehensive Cancer Center

Locations

Jonsson Comprehensive Cancer Center at UCLA

Los Angeles, California, United States

Countries

United States

Other Identifiers

P50CA090388

Identifier Type: NIH

Identifier Source: secondary_id

View Link

P30CA016042

Identifier Type: NIH

Identifier Source: secondary_id

View Link

UCLA-0407058-01

Identifier Type: -

Identifier Source: secondary_id

CDR0000407580

Identifier Type: -

Identifier Source: org_study_id