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OpenTrials
Completed

NCT Number: NCT00173875

Iressa as a First-Line Treatment in Chemonaive Patients With Inoperable Non-Small Cell Lung Cancer

The purpose of this study is to assess the overall response rate to Iressa as a first-line treatment in chemonaive patients with inoperable Non-Small Cell Lung Cancer (NSCLC)

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Oncology, National Taiwan University Hospital

Taipei, Taiwan

About this study

The epidermal growth factor receptor (EGFR) is a promising target for anticancer therapy because it is expressed or highly expressed in a variety of tumors, including NSCLC.Furthermore, high levels of EGFR expression have been associated with a poor prognosis in lung cancer patients in several studies. EGFR-targeted cancer therapies are currently being developed; strategies include inhibition of the intracellular tyrosine kinase domain of the receptor by small molecules such as gefitinib (Iressa [ZD1839]; AstraZeneca, Wilmington, DE). Iressa is an orally active, selective EGFR tyrosine kinase inhibitor that blocks signal transduction pathways implicated in the proliferation and survival of cancer cells.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically or cytologically confirmed stage IIIB/IV NSCLC
  • No immediate need for palliative radiotherapy and No prior chemotherapy
  • age > 20 Y/O
  • ECOG PS: 0 - 2
  • ANC >2000
  • PLT >100k
  • Hb > 10
  • total bilirubin < 2.0 mg/dL
  • serum creatinine < 2 mg/dl
  • SGPT and SGOT < 2.5 ×ULN, alkaline phosphatase < 5 ×ULN
  • life expectancy >6mos.

Exclusion criteria

  • If the patients have brain metastases or receive radiotherapy, the disease must be stable for more than 6 weeks after the last dose of radiotherapy
  • 2nd malignancies
  • Unable to swallow tablets
  • Patients (M/F) with reproductive potential not implementing adequate contraceptive measurements
  • Pregnant or lactating patients
  • Participation in other clinical trials within 30 days of study entry
  • Major systemic disease which in the investigator's opinion might confound the clinical trial

Treatment and study plan

Iressa

Drug

Primary outcomes

  1. The primary objective of this study is to assess the overall response rate to Iressa as a first-line treatment in chemonaive patients with inoperable Non-Small Cell Lung Cancer

    Time frame: 2005~2007

Secondary outcomes

  1. To evaluate 1) Individual response rate 2) Time to progression 3) Overall survival (OS) at year1 4) Progression free survival (PFS) at year1 5) Toxicity

    Time frame: 2005~2007

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

A Phase II Study to Evaluate the Efficacy and Safety of Iressa as a First-Line Treatment in Chemonaive Patients With Inoperable Non-Small Cell Lung Cancer (NSCLC)

Important dates

Study start
2005
Study completion
2007
First posted
Sep 15, 2005
Registry last updated
Jul 30, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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