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Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches - Proceedings of the 18th Annual Detroit Cancer Symposium Detroit, Michigan, USA - June 13-14, 1986 (Paperback, Softcover reprint of the original 1st ed. 1986)
Loot Price: R4,251
Discovery Miles 42 510
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Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches - Proceedings of the 18th Annual Detroit Cancer Symposium Detroit, Michigan, USA - June 13-14, 1986 (Paperback, Softcover reprint of the original 1st ed. 1986)
Series: Developments in Oncology, 47
Expected to ship within 10 - 15 working days
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Biochemical Modulation at the present time defines an area of study
in which the intracellular metabolism of a given anti cancer agent
is modulated (usually by a noncytotoxic agent or a cytotoxic agent
at sufficiently low dosage to make it non cytotoxic) in order to
either increase the effectiveness of the particular agent against
tumor cells or decrease its cytotox icity against normal cells. The
major focus of modulation has been the agents 5-fluorouracil
(FUra), arabinofuranosylcytosine (ara-C), methotrexate (MTX) and a
few alkylating agents. The major thrust of the studies has been to
increase the flow of the anticancer agent along the pathway
responsible for the formation of the cytotoxic species: for
example, FUra to FUTP or ara-C to ara-CTP. While in most cases the
application of research re sults to clinical trials does not
require the subsequent exper tise of the laboratory researchers,
application of biochemical modulatory schemes to clinical protocols
necessitate a dramatic break with the past procedures. As shown in
the laboratory clinical loop below, close collaboration between the
laboratory and clinical investigator is essential. While the
laboratory REDEFINE TECHNOLOGY, TESTS OR QUESTIONS FOR FURTHER
THERAPEUTIC ADVANCE CLINICAL EXPERIMENTAL PROTOCOL (LABORATORY)
RESEARCH STUDIES DEFINE AND TEST APPROPRIATE SCIENTIFIC PARAMETERS
results define rationally-based regimens, it is essential that the
clinical protocols contain the requirement that clinical material
(either tumor or normal tissues) be sampled to deter mine whether
the biochemical modulation being proposed is in fact beinq
accomplished.
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