Ftorafur, adriamycin, cyclophosphamide and BCG in the treatment of metastatic breast cancer. 1979

G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey

Ftorafur is a 5-fluorouracil analogue which is slowly metabolized to 5-FU, resulting in prolonged therapeutic levels of this latter drug. Ninety-one evaluable patients with metastatic breast cancer were treated with Ftorafur, Adriamycin, cyclophosphamide, and BCG (ACFTOR-BCG), in an attempt to increase the effectiveness of the program or decrease its myelosuppressive toxicity. The results of this trial were compared to those previously reported with the combination of 5-FU, Adriamycin, cyclophosphamide, and BCG (FAC-BCG). Overall objective response rates were 65% and 76% for ACFTOR-BCG and FAC-BCG, respectively. Durations of response were 12 months and 14 months for ACFTOR-BCG and FAC-BCG (p = 0.53). The median survival of responders was 22 and 23.9 months, respectively. Substantial toxicity was observed with Ftorafur: nausea and vomiting severe enough to cause weight loss was observed in a substantially higher fraction of the patients treated with this drug than with 5-FU. Other side-effects, which were not observed with the 5-FU combination, were somnolence, dizziness, personality changes, tremor, ataxia, and confusion. No differences in myelosuppressive toxicity were observed between the two combinations, and the incidence of infectious complications was identical. The combination of Ftorafur, Adriamycin, cyclophosphamide and BCG did not offer any advantages with respect to increased effectiveness or reduced toxicity over the FAC-BCG regimen in breast carcinoma.

UI MeSH Term Description Entries
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D001835 Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. Body Weights,Weight, Body,Weights, Body
D001943 Breast Neoplasms Tumors or cancer of the human BREAST. Breast Cancer,Breast Tumors,Cancer of Breast,Breast Carcinoma,Cancer of the Breast,Human Mammary Carcinoma,Malignant Neoplasm of Breast,Malignant Tumor of Breast,Mammary Cancer,Mammary Carcinoma, Human,Mammary Neoplasm, Human,Mammary Neoplasms, Human,Neoplasms, Breast,Tumors, Breast,Breast Carcinomas,Breast Malignant Neoplasm,Breast Malignant Neoplasms,Breast Malignant Tumor,Breast Malignant Tumors,Breast Neoplasm,Breast Tumor,Cancer, Breast,Cancer, Mammary,Cancers, Mammary,Carcinoma, Breast,Carcinoma, Human Mammary,Carcinomas, Breast,Carcinomas, Human Mammary,Human Mammary Carcinomas,Human Mammary Neoplasm,Human Mammary Neoplasms,Mammary Cancers,Mammary Carcinomas, Human,Neoplasm, Breast,Neoplasm, Human Mammary,Neoplasms, Human Mammary,Tumor, Breast
D002490 Central Nervous System The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges. Cerebrospinal Axis,Axi, Cerebrospinal,Axis, Cerebrospinal,Central Nervous Systems,Cerebrospinal Axi,Nervous System, Central,Nervous Systems, Central,Systems, Central Nervous
D003520 Cyclophosphamide Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate,B-518,Cyclophosphamide Anhydrous,Cyclophosphamide Monohydrate,Cyclophosphamide, (R)-Isomer,Cyclophosphamide, (S)-Isomer,Cyclophosphane,Cytophosphan,Cytophosphane,Cytoxan,Endoxan,NSC-26271,Neosar,Procytox,Sendoxan,B 518,B518,NSC 26271,NSC26271
D004317 Doxorubicin Antineoplastic antibiotic obtained from Streptomyces peucetius. It is a hydroxy derivative of DAUNORUBICIN. Adriamycin,Adriablastin,Adriablastine,Adriblastin,Adriblastina,Adriblastine,Adrimedac,DOXO-cell,Doxolem,Doxorubicin Hexal,Doxorubicin Hydrochloride,Doxorubicin NC,Doxorubicina Ferrer Farm,Doxorubicina Funk,Doxorubicina Tedec,Doxorubicine Baxter,Doxotec,Farmiblastina,Myocet,Onkodox,Ribodoxo,Rubex,Urokit Doxo-cell,DOXO cell,Hydrochloride, Doxorubicin,Urokit Doxo cell
D004359 Drug Therapy, Combination Therapy with two or more separate preparations given for a combined effect. Combination Chemotherapy,Polychemotherapy,Chemotherapy, Combination,Combination Drug Therapy,Drug Polytherapy,Therapy, Combination Drug,Chemotherapies, Combination,Combination Chemotherapies,Combination Drug Therapies,Drug Polytherapies,Drug Therapies, Combination,Polychemotherapies,Polytherapies, Drug,Polytherapy, Drug,Therapies, Combination Drug
D005260 Female Females
D005472 Fluorouracil A pyrimidine analog that is an antineoplastic antimetabolite. It interferes with DNA synthesis by blocking the THYMIDYLATE SYNTHETASE conversion of deoxyuridylic acid to thymidylic acid. 5-FU,5-FU Lederle,5-FU Medac,5-Fluorouracil,5-Fluorouracil-Biosyn,5-HU Hexal,5FU,Adrucil,Carac,Efudex,Efudix,Fluoro-Uracile ICN,Fluoroplex,Fluorouracil Mononitrate,Fluorouracil Monopotassium Salt,Fluorouracil Monosodium Salt,Fluorouracil Potassium Salt,Fluorouracil-GRY,Fluorouracile Dakota,Fluorouracilo Ferrer Far,Fluoruracil,Fluracedyl,Flurodex,Haemato-FU,Neofluor,Onkofluor,Ribofluor,5 FU Lederle,5 FU Medac,5 Fluorouracil,5 Fluorouracil Biosyn,5 HU Hexal,Dakota, Fluorouracile,Fluoro Uracile ICN,Fluorouracil GRY,Haemato FU
D005641 Tegafur Congener of FLUOROURACIL with comparable antineoplastic action. It has been suggested especially for the treatment of breast neoplasms. 1-(2-Tetrahydrofuryl)-5-fluorouracil,1-(Tetrahydro-2-furanyl)-5-fluorouracil,5-Fluoro-1-(tetrahydro-2-furanyl)-2,4-pyrimidinedione,FT-207,FT207,Florafur,Fluorofur,Ftorafur,Futraful,N1-(2'-Tetrahydrofuryl)-5-fluorouracil,Sunfural S,Uftoral,Utefos,FT 207

Related Publications

G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
September 1984, Gan to kagaku ryoho. Cancer & chemotherapy,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1984, Cancer chemotherapy and pharmacology,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1988, Gan to kagaku ryoho. Cancer & chemotherapy,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
December 1988, Gan to kagaku ryoho. Cancer & chemotherapy,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
December 1977, Cancer treatment reports,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1983, Orvosi hetilap,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1991, Neoplasma,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
August 1988, American journal of clinical oncology,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1989, Oncology,
G N Hortobagyi, and G R Blumenschein, and C K Tashima, and A U Buzdar, and M A Burgess, and R B Livingston, and M Valdivieso, and J U Gutterman, and E M Hersh, and G P Bodey
January 1984, Neoplasma,
Copied contents to your clipboard!