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Developing new drugs for the treatment of lymphoma.

Developing new drugs for the treatment of lymphoma. Research Abstract Details 

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  • Developing new drugs for the treatment of lymphoma. Abstract Text:

    Despite the great progress that has been made over the last several decades in the treatment of lymphoma, the prognosis for patients with relapsed disease, and particular sub-types of lymphoma like mantle cell and T cell lymphoma, remains quite poor. While major advances in the use of combination chemotherapy, monoclonal antibodies, peripheral blood stem cell transplants, and radioimmunotherapy, have provided new opportunities to alter the natural history of these diseases, and even improve cure rates among elected sub-populations of patients, these 'traditional' approaches have not benefited all patients, or subtypes of lymphoma. The incredibly rapid pace of understanding the molecular basis for the discrete sub-types of both non-Hodgkin's lymphoma and Hodgkin's Disease is beginning to afford exciting new opportunities to both risk stratify patients, and to identify potentially novel 'drugable' targets. These advancements in understanding the major molecular defects in lymphoma, have provided a new context in which we can rethink the use of new and old drugs, and design new ones with unique mechanisms of action. The panoply of new targets and drugs now becoming available for the treatment of lymphoma is truly daunting. A plethora of new small molecules that target bcl-2, mTOR, histone deactylases, and NF-kB have shown promising preclinical activity, and are now promising early phase activity. In many cases, the empirical observations from early clinical trials have provided invaluable clues to potentially valuable drugs like bortezomib, depsipeptide, and SAHA, These empirical observations, based on the inclusion of patients with lymphoma on these studies, have thus far proven to be as or more valuable than any other 'rational' target based approach. In addition, beyond the novel small molecules affecting unique and heretofore unrecognized biological pathways, there continues to be a robust and important effort to identify new derivatives of older generation drugs with hopefully better activity, and less toxicity. For example, new generation anthracenediones and anti-folates, and new formations of older drugs like doxorubicin, irinotecan, and vincristine afford new opportunities to favourably change the pharmacokinetic profile of these agents, and improve their overall safety profile. While it would not be possible to address each and every new such drug, we hope to touch on some of the major new themes and agents emerging for the treatment of Hodgkin's Disease and non-Hodgkin's lymphoma.

    Developing new drugs for the treatment of lymphoma. Publishing Authors By Initials

    For similar neoplasms: neoplasms by histologic type: lymphoma research abstracts see: neoplasms: neoplasms by histologic type: lymphoma research

    PUBMED ID PMID:

    MEDLINE DATE:

    Developing new drugs for the treatment of lymphoma. Journal Published:

    PUBLICATION TYPE: Review

    Journal: European journal of haematology. Supplementum

    VOLUME:

    Page Numbers: 150-8

    Journal Abbreviation:

    ISSN: 0902-4506

    DAY: 26

    MONTH: Jul

    YEAR: 2005

    Developing new drugs for the treatment of lymphoma. Information

    Number of References: 41

    LANGUAGE: eng

    NlmUniqueID: 8703474

    Developing new drugs for the treatment of lymphoma. Keywords Mesh Terms:

    KEYWORDS: Lymphoma

    MESH TERMS: drug therapy

    Chemical & Substance for Abstract: Developing new drugs for the treatment of lymphoma. Information

    Substance Name: Antineoplastic Agents

    Registry Number: 0

    Grant and Affiliation Information for Developing new drugs for the treatment of lymphoma.

    AFFILIATION: Department of Medicine, Memorial Sloan Kettering Cancer Center, Lymphoma and Developmental Chemotherapy Services, Box 329, 1275 York Ave., New York, NY 10021, USA. oconnoro@mskcc.org

    Country: Denmark

    Denmark Research PublicationDenmark Research Publication

    AGENCY: United States NCI

    GRANT: UO1 CA 69913

    ACRONYM: CA

    MEDLINETA: Eur J Haematol Suppl

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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