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Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation.

Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Research Abstract Details 

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  • Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Abstract Text:

    maneesh jainManeesh Jain,ganesh venkatramanGanesh Venkatraman,surinder k batraSurinder K Batra,

    In contrast to the overwhelming success of radiolabeled antibodies in treating hematologic malignancies, only modest success has been achieved in the radioimmunotherapy of solid tumors. One of the major limitations in successful application of radioimmunotherapy is the large molecular size of the intact immunoglobulin that results in prolonged serum half-life and poor tumor penetration and uptake. With the advent of antibody engineering, small molecular weight antibody fragments exhibiting improved pharmacokinetics and tumor penetration have been generated. However, their clinical application has been limited by suboptimal tumor uptake and short tumor residence time. There is a greater realization that optimization of the molecular size of the antibodies alone is not sufficient for clinical success of radioimmunotherapy. In addition to their size, radiolabeled antibodies encounter other impediments before reaching their target antigens expressed on the cell surface of solid tumors. Some of the barriers include poor blood flow in large tumors, permeability of vascular endothelium, elevated interstitial fluid pressure of tumor stroma, and heterogeneous antigen expression. Recent research has considerably improved our understanding and appreciation of these forces, and the new wave of optimization strategies involves the use of biological modifiers to modulate the impediments posed by solid tumors. In combination with radiolabeled antibodies, various agents are being used to improve the tumor blood flow, enhance vascular permeability, lower tumor interstitial fluid pressure by modulating stromal cells and extracellular matrix components, up-regulate the expression of target antigens, and improve the penetration and retention of the radiopharmaceuticals. This review outlines ongoing research efforts involving biological modifiers to optimize the uptake and efficacy of radiolabeled antibodies for the treatment of solid tumors.

    Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Publishing Authors By Initials

    m jainM Jain,g venkatramanG Venkatraman,sk batraSK Batra,

    For similar therapeutics: biological therapy: immunotherapy: radioimmunotherapy research abstracts see: therapeutics: biological therapy: immunotherapy: radioimmunotherapy research

    PUBMED ID PMID:

    MEDLINE DATE:

    Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Clinical cancer research : an official journal of

    VOLUME: 13

    Page Numbers: 1374-82

    Journal Abbreviation: Clin. Cancer Res.

    ISSN: 1078-0432

    DAY: 19

    MONTH: 02

    YEAR: 2007

    Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Information

    Number of References: 97

    LANGUAGE: eng

    NlmUniqueID: 9502500

    Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Keywords Mesh Terms:

    KEYWORDS: Radioimmunotherapy

    MESH TERMS: methods

    Chemical & Substance for Abstract: Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation. Information

    Substance Name: Antibodies

    Registry Number: 0

    Grant and Affiliation Information for Optimization of radioimmunotherapy of solid tumors: biological impediments and their modulation.

    AFFILIATION: Department of Biochemistry and Molecular Biology, Department of Pathology and Microbiology, Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198-5870, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA78590

    ACRONYM: CA

    MEDLINETA: Clin Cancer Res

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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