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A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer.

A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Research Abstract Details 

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  • A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Abstract Text:

    sheri k dennisonSheri K Dennison,samuel a jacobsSamuel A Jacobs,john w wilsonJohn W Wilson,janell seegerJanell Seeger,terrence p cesconTerrence P Cescon,jane m raymondJane M Raymond,charles e geyerCharles E Geyer,norman wolmarkNorman Wolmark,sandra m swainSandra M Swain,

    This was a phase II multi-institutional trial to determine the efficacy and tolerability of gefitinib (Iressatrade) and docetaxel as first-line treatment in patients with metastatic breast cancer. All patients had histologically confirmed breast cancer with metastatic disease. They were permitted to have received adjuvant chemotherapy, but no prior docetaxel or prior chemotherapy for metastatic disease. Patients received gefitinib 250 mg once daily and docetaxel 75 mg/m(2) every 3 weeks, until tumor progression, toxicity or other reasons for discontinuation. Thirty-three patients were enrolled and received a median of 5 cycles of treatment. The clinical benefit rate was 51.5% (95% CI: 33.5-69.2%). There were 1 confirmed complete response and 12 confirmed partial responses, and the overall objective response rate was 39.4% (95% CI: 22.9-57.9%). Four patients had stable disease for > or =24 weeks. The median duration of clinical benefit was 10.9 months (95% CI: 6.0-17.6 months). The most common reason for study discontinuation was disease progression (16 patients), followed by toxicity (ten patients). Toxicities were mainly attributable to docetaxel, including > or =grade 3 neutropenia in 43% of patients. The combination of gefitinib and docetaxel is an active regimen in patients with previously untreated metastatic breast cancer, with a clinical benefit rate and toxicity profile in the range of that reported for docetaxel alone.

    A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Publishing Authors By Initials

    sk dennisonSK Dennison,sa jacobsSA Jacobs,jw wilsonJW Wilson,j seegerJ Seeger,tp cesconTP Cescon,jm raymondJM Raymond,ce geyerCE Geyer,n wolmarkN Wolmark,sm swainSM Swain,

    For similar abstracts research abstracts see: abstracts research

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    A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Investigational new drugs

    VOLUME: 25

    Page Numbers: 545-51

    Journal Abbreviation:

    ISSN: 0167-6997

    DAY: 12

    MONTH: 06

    YEAR: 2007

    A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Information

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    LANGUAGE: eng

    NlmUniqueID: 8309330

    A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer. Keywords Mesh Terms:

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    Grant and Affiliation Information for A phase II clinical trial of ZD1839 (Iressa) in combination with docetaxel as first-line treatment in patients with advanced breast cancer.

    AFFILIATION: Walter Reed Army Medical Center, 6900 Georgia Ave. NW, Washington, DC 20307, USA. dennisonsk@mail.nih.gov

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Invest New Drugs

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