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Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future.

Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Research Abstract Details 

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  • Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Abstract Text:

    robert g makiRobert G Maki,

    Objective. In the era of oral molecular kinase inhibitors, cytotoxic chemotherapy agents are somewhat overlooked, but remain the backbone of treatment for most cancers. Patients with non-gastrointestinal stromal tumor sarcomas, such as leiomyosarcoma, liposarcoma, and undifferentiated high-grade pleomorphic sarcoma (formerly called malignant fibrous histiocytoma), have received doxorubicin and ifosfamide as the backbone of their treatment for over 15 years or more. The goal of this article is to review the data that have led to the use of gemcitabine and docetaxel as a useful combination for patients with metastatic sarcomas, and to comment on possible synergy of the combination. Methods and results. The literature regarding the use of gemcitabine, docetaxel, or both, is reviewed, with emphasis on patients with metastatic sarcoma. Results. Activity of gemcitabine and docetaxel is observed in leiomyosarcoma and undifferentiated high-grade pleomorphic sarcoma. There is apparent schedule dependence of the combination in other cancers; it is unclear if schedule matters in patients with sarcomas. The dose and schedule of gemcitabine and docetaxel examined in phase II studies are probably too high for routine practice. Conclusions. The combination of gemcitabine and docetaxel is an effective option for patients with metastatic sarcoma, increasing the armamentarium for the practicing oncologist in treating this heterogeneous group of diseases. Given the low response rate to docetaxel as a single agent, it is likely that there is true clinical synergy of the combination. Disclosure of potential conflicts of interest is found at the end of this article.

    Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Publishing Authors By Initials

    rg makiRG Maki,

    For similar organic chemicals: hydrocarbons: hydrocarbons, cyclic: hydrocarbons, alicyclic: cycloparaffins: cyclodecanes: taxoids research abstracts see: organic chemicals: hydrocarbons: hydrocarbons, cyclic: hydrocarbons, alicyclic: cycloparaffins: cyclodecanes: taxoids research

    PUBMED ID PMID:

    MEDLINE DATE:

    Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Journal Published:

    PUBLICATION TYPE: Review

    Journal: The oncologist

    VOLUME: 12

    Page Numbers: 999-1006

    Journal Abbreviation: Oncologist

    ISSN: 1083-7159

    DAY: 3

    MONTH: Aug

    YEAR: 2007

    Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Information

    Number of References: 44

    LANGUAGE: eng

    NlmUniqueID: 9607837

    Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Keywords Mesh Terms:

    KEYWORDS: Taxoids

    MESH TERMS: therapeutic use

    Chemical & Substance for Abstract: Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future. Information

    Substance Name: Deoxycytidine

    Registry Number: 951-77-9

    Grant and Affiliation Information for Gemcitabine and docetaxel in metastatic sarcoma: past, present, and future.

    AFFILIATION: Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, New York 10021-6007, USA. makir@mskcc.org.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: P01-CA47179

    ACRONYM: CA

    MEDLINETA: Oncologist

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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