Clinical Trials/NCT00075439

NCT00075439CompletedPhase 2

A Phase II Trial of ZD1839 (Iressa®) in Metastatic Neuroendocrine Tumors

National Cancer Institute (NCI)1 site in 1 country90 target enrollmentStarted: December 2003Last updated: June 4, 2013

Conditions

Interventions

Drugs

Trial Snapshot

Phase: Phase 2
Status: Completed
Sponsor: National Cancer Institute (NCI)
Enrollment: 90
Locations: 1
Primary Endpoint: Proportion of patients progression-free at 6 months

Study Overview Study Design Eligibility Criteria Arms & Interventions Outcomes Investigators Sites Records & Identifiers Similar Trials

Study Overview

Brief Summary

This phase II trial is studying how well gefitinib works in treating patients with progressive metastatic neuroendocrine tumors. Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine the 6 month progression free survival rate in patients with progressive, advanced neuroendocrine tumors treated with ZD1839.

SECONDARY OBJECTIVES:

I. Objective tumor response rate. II. Progression free survival and time to progression. III. Improvement in circulating hormone levels. IV. Overall survival V. We will explore the molecular characterization of these tumors in attempt to understand the role of EGFR expression and its inhibition with ZD1839 in neuroendocrine tumors. The measurements will be performed on pretreatment and post-treatment tumor biopsies when possible: EGFR expression and gene amplification (IHC for EGFR and phosphorylated EGFR, ISH for gene amplification); Activation of the Ras/Raf/MAPK pathway (IHC for phosphorylated MAPK); Cell proliferation (Ki-67 staining); Apoptosis (TUNEL assay).

OUTLINE: This is a multicenter study. Patients are stratified according to disease type (carcinoid vs islet cell and other neuroendocrine tumors).

Study Design

Study Type: Interventional
Allocation: Na
Intervention Model: Single Group
Primary Purpose: Treatment
Masking: None

Eligibility Criteria

Ages: 18 Years to — (Adult, Older Adult)
Sex: All
Accepts Healthy Volunteers: No

Inclusion Criteria

•Histologically confirmed metastatic neuroendocrine neoplasms or histologic confirmation of primary neuroendocrine tumor with clear clinical evidence of metastases
•Measurable disease
•Radiographic evidence of disease progression, following any prior systemic therapy, chemoembolization, embolization, or observation; for eligibility purposes, disease progression will be defined as follows:
•Either of the following documented by comparison of the on-study radiographic assessment with a prior assessment of the same type performed within the previous 60 calendar weeks:
•Appearance of a new lesion
•At least 20% increase in the longest diameter (LD) of any previously documented lesion or an increase in the sum of the LDs of multiple lesions in aggregate of 20%
•≥4 weeks from the completion of major surgery, chemotherapy or other systemic therapy and hepatic artery embolization/chemoembolization to study registration
•≥3 weeks from the completion of radiation therapy to study registration
•Recovered sufficiently from side effects of prior therapy
•Absolute neutrophil count (ANC) ≥ 1000/mm3
•PLT ≥ 75,000/ mm3
•Hgb ≥ 8.0 g/dL
•Total bilirubin ≤ 2 x upper normal limit (UNL)
•Alkaline phosphatase ≤ 3 x UNL (5 x UNL if liver metastases present)
•AST ≤ 3 x UNL (≤ 5 x UNL if liver metastases present)
•Creatinine ≤ 1.5 x UNL
•ECOG performance score (ps) ≤ 2
•Life expectancy ≥ 24 weeks
•Capable of understanding the investigational nature, potential risks and benefits of the study and able to provide valid informed consent

Exclusion Criteria

•Thyroid carcinoma of any histology or pheochromocytoma/paraganglioma
•Any of the following as this regimen may be harmful to a developing fetus or nursing child:
•Pregnant women
•Breastfeeding women
•Men or women of childbearing potential or their sexual partners who are unwilling to employ adequate contraception (condoms, diaphragm, birth control pills, injections, intrauterine device [IUD], surgical sterilization, subcutaneous implants, or abstinence, etc.)
•NOTE: The effects of the agent(s) on the developing human fetus at the recommended therapeutic dose are unknown
•Anaplastic or high-grade histology
•Any of the following prior therapies:
•> 1 prior systemic chemotherapy regimen (chemoembolization not counted as systemic chemotherapy)
•Prior EGFR targeted regimen (e.g. OSI-774, EKB-569, ZD1839)
•< 4 weeks from last Interferon injection
•< 2 weeks from last octreatide short acting injection or < 6 weeks long acting injection; Note: concurrent octreatide allowed if stable dose has been administered for ≥1 month, there is documented tumor progression on the current dose, and there is no current plan for increasing dose • Other concurrent treatment considered investigational
•Concurrent chemotherapy or radiation therapy
•Any of the following:
•Gastrointestinal tract disease resulting in an inability to take oral medication (e.g. dysphagia or inability to swallow capsules intact).
•Requirement for IV alimentation
•Prior procedures clearly adversely affecting intestinal absorption
•Active peptic ulcer disease
•Failure to fully recover from adverse effects of prior therapies regardless of interval since last treatment
•Known abnormality of cornea, such as:
•History of dry eye syndrome or Sjogren syndrome
•Congenital abnormality
•Abnormal slit-lamp examination using a vital dye (e.g.: fluorescein or Bengal-rose)
•Abnormal corneal sensitivity test (Schirmer test)
•Uncontrolled intercurrent illness including, but not limited to:
•Ongoing or active infection
•Symptoms of congestive heart failure
•Unstable angina pectoris, cardiac arrhythmia
•Psychiatric illness/social situation that would limit compliance with study requirement
•Known brain metastases; Note: These patients are excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events
•Known HIV-positive patients receiving combination anti-retroviral therapy; Note: These patients are excluded from the study because of possible pharmacokinetic interactions with ZD1839 and because patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy; appropriate studies will be undertaken in patients receiving combination and anti-retroviral therapy when indicated
•Concurrent or recent use (≤ 7 days prior to ZD1839 administration) of phenytoin, carbamazepine, barbiturates, rifampicin, oxcarbazepine, rifapentine, modafinil, or St. John's Wort; Note: Because these drugs induce CYP3A4 enzymes and can cause reductions in ZD1839 plasma concentrations below levels thought to be biologically active, patients with concurrent or recent use of these drugs are excluded from the study
•History of other invasive malignancy ≤ the previous 3 years, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix

Arms & Interventions

Arm I

Experimental

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

Intervention: gefitinib (Drug)

Arm I

Experimental

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

Intervention: laboratory biomarker analysis (Other)

Outcomes

Primary Outcomes

Proportion of patients progression-free at 6 months

Time Frame: At 6 months

If patients are lost to follow-up or discontinue active monitoring prior to 6 months post-registration, we will consider censoring them for the evaluation of the primary endpoint. Here, Kaplan-Meier methodology will be used to estimate the final success proportion (ie, 6 month success rate with a 95% confidence interval). Otherwise, ninety-five percent confidence intervals for the true success proportion will be calculated according to the approach of Duffy and Santner.

Secondary Outcomes

Incidence of adverse events graded according to NCI CTCAE version 3.0(Up to 2 years)
Confirmed tumor response to treatment will be evaluated and will be considered a PR or CR on consecutive evaluations at least 4 weeks apart(Up to 2 years)
Survival time(Time from registration to death due to any cause, assessed up to 2 years)
Time to disease progression(Time from randomization to documentation of disease progression, assessed up to 2 years)
Duration of response(Date from which the patient's objective status is first noted to be either a CR or PR to the date progression is documented, assessed up to 2 years)
Time to treatment failure(Time from the date of registration to the date at which the patient is removed from treatment due to progression, toxicity, refusal, or death, assessed up to 2 years)

Investigators

Sponsor

National Cancer Institute (NCI)

Sponsor Class

Nih

Responsible Party

Sponsor

Study Sites (1)

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