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Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943).

Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Research Abstract Details 

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  • Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Abstract Text:

    r j woodmanR J Woodman,r l cysykR L Cysyk,i klineI Kline,m gangM Gang,j m vendittiJ M Venditti,

    The LD50 of intraperitoneally (ip) injected daunorubicin in nonleukemic mice (1.8 mg/kg, q4d times 3) can be increased several fold by the concomitant ip injection of ICRF-159. In addition, the survival of leukemic mice treated with daunorubicin and ICRF-159 on Days 1, 5, and 9 after ip inoculation of L1210 tumor cells was substantially greater than after treatment with either drug alone. This potentiation of survival with combination treatment usually occurred with doses of daunorubicin greater than the LD50 of daunorubicin alone. The LD50 of subcutaneously (sc) injected daunorubicin alone (14.0 mg/kg, q4d times 3) was not increased by concomitant ip treatment with ICRF-159. However, when leukemic mice were treated sc with daunorubicin and ip with ICRF-159 on Days 1, 5, and 9 after ip injection of L1210 leukemia cells, survival was greater than with treatment with either drug alone. The toxicity of ip injected adriamycin was not reduced by ICRF-159, but treatment of leukemic mice with this combination was more effective in prolonging survival than treatment with either drug alone. Combination treatment with daunorubicin plus ICRF-159 showed much less therapeutic enhancement against sc implanted L1210 leukemia than against the ip implanted tumor.

    Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Publishing Authors By Initials

    rj woodmanRJ Woodman,rl cysykRL Cysyk,i klineI Kline,m gangM Gang,jm vendittiJM Venditti,

    For similar natural sciences: time: time factors research abstracts see: natural sciences: time: time factors research

    PUBMED ID PMID:

    MEDLINE DATE: 1975 Jul-Aug

    Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Cancer chemotherapy reports. Part 1

    VOLUME: 59

    Page Numbers: 689-95

    Journal Abbreviation:

    ISSN: 0069-0112

    DAY: 20

    MONTH: 02

    YEAR: 2008

    Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7607105

    Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Keywords Mesh Terms:

    KEYWORDS: Time Factors

    MESH TERMS: toxicity

    Chemical & Substance for Abstract: Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943). Information

    Substance Name: Doxorubicin

    Registry Number: 23214-92-8

    Grant and Affiliation Information for Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943).

    AFFILIATION:

    Country: UNITED STATES

    UNITED STATES Research PublicationUNITED STATES Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Cancer Chemother Rep

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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    Enhancement of the effectiveness of daunorubicin NSC-82151 or adriamycin NSC-123127 against early mouse L1210 leukemia with ICRF-159 NSC-129943 Related Publications

     

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