Literature DB >> 6793224

One-day VATH (vinblastine, Adriamycin, thiotepa, and Halotestin) therapy for advanced breast cancer refractory to chemotherapy.

R D Hart, M Perloff, J F Holland.   

Abstract

Twenty-nine postmenopausal patients with metastatic breast cancer refractory to conventional combination chemotherapy underwent treatment with a combination of vinblastine, Adriamycin, thiotepa, and Halotestin given once every 21 days. Thirteen patients (45%) responded with a greater than 50% regression of measurable tumor. Responses occurred in nine of 12 patients (75%) with visceral dominant disease and were recognized in four of 15 (27%) with osseous dominant disease (another 5 improved for a total improvement of 60%). The median duration of response was 11 months. The median survival times were 16 months for responders and eight months for those with progressive disease. Response rate was not affected by age, number of years after menopause, number of metastatic sites involved, or number of systemic treatment modalities previously used, but may have been adversely affected by late stage at original diagnosis, short time from diagnosis, poor response to primary chemotherapy, and dose modification. This combination of drugs is a convenient, tolerable, and effective regimen for treating breast cancer refractory to primary chemotherapy regimens currently in use.

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Year:  1981        PMID: 6793224     DOI: 10.1002/1097-0142(19811001)48:7<1522::aid-cncr2820480709>3.0.co;2-g

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  11 in total

1.  Single and repeated dose pharmacokinetics of thio-TEPA in patients treated for ovarian carcinoma.

Authors:  B Hagen; F Walseth; R A Walstad; T Iversen; O G Nilsen
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

2.  Adriamycin, vinblastine and mitomycin C as second-line chemotherapy in advanced breast cancer.

Authors:  A Sulkes; E Gez; M R Pfeffer; R Catane; R Isacson; S Biran
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

3.  A phase II study of thioTEPA in children with recurrent solid tumor malignancies: a Children's Cancer Group study.

Authors:  J R Geyer; F M Balis; M D Krailo; R Heideman; E Broxson; J K Sato; D Poplack; W A Bleyer
Journal:  Invest New Drugs       Date:  1996       Impact factor: 3.850

4.  Pharmacokinetics of thio-TEPA at two different doses.

Authors:  B Hagen; R A Walstad; O G Nilsen
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

Review 5.  Postmenopausal breast cancer. Drug therapy in the 1990s.

Authors:  C I Falkson; G Falkson; H C Falkson
Journal:  Drugs Aging       Date:  1993 Mar-Apr       Impact factor: 3.923

Review 6.  Managing breast cancer in an outpatient setting.

Authors:  F M Muggia
Journal:  Breast Cancer Res Treat       Date:  1992       Impact factor: 4.872

7.  On the search for new anticancer drugs 14: the plasma pharmacokinetics and tissue distribution of spin-labeled thio-TEPA (SL-O-TT).

Authors:  P L Gutierrez; B E Cohen; G Sosnovsky; T A Davis; M J Egorin
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

8.  Vincristine, doxorubicin and mitomycin (VAM) in patients with advanced breast cancer previously treated with cyclophosphamide, methotrexate and fluorouracil (CMF). A clinical trial of the Piedmont Oncology Association (POA).

Authors:  S K Shipp; H B Muss; M A Westrick; M R Cooper; D V Jackson; F C Richards; D R White; J J Stuart; R M Christian; W Ramseur
Journal:  Cancer Chemother Pharmacol       Date:  1983       Impact factor: 3.333

Review 9.  Chemotherapy of breast cancer.

Authors:  L S Perlow; J F Holland
Journal:  Med Oncol Tumor Pharmacother       Date:  1984

10.  Adjuvant therapy of breast cancer 1971-1981. Ten years of progress.

Authors:  P P Carbone
Journal:  Breast Cancer Res Treat       Date:  1982       Impact factor: 4.872

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