Literature DB >> 3791561

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

A Sulkes, E Gez, M R Pfeffer, R Catane, R Isacson, S Biran.   

Abstract

Thirty-six evaluable patients with metastatic measurable breast carcinoma previously treated with CMF or CMFVP were given second-line chemotherapy with Adriamycin, vinblastine, and mitomycin C (AVM), as follows: Adriamycin 20 mg/m2 and vinblastine 6 mg/m2 by i. v. push on days 1, 8, and 15, and mitomycin C 10 mg/m2 i. v. on day 1, every 6 weeks. Ten patients (28%) achieved partial remission (PR) lasting a median of 10 months, and eight patients (22%) experienced improvement of a lesser level than PR. An additional nine patients (25%) had disease stabilization; in the remaining nine patients (25%), persistent disease progression was observed. The median survival from the onset of AVM was 7 months for all patients; patients with PR survived a median of 13 months. Myelotoxicity was substantial and frequently interfered with the optimal administration of AVM, especially in patients with skeletal metastases; four patients were hospitalized with leukopenia and fever; all recovered promptly; one death was probably related to thrombocytopenia and CNS bleeding. Our results with AVM are similar to the average response rate published in the literature with the use of Adriamycin as a single agent in previously treated patients with advanced breast cancer.

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Year:  1986        PMID: 3791561     DOI: 10.1007/bf00262288

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  32 in total

1.  Sequential administration of two oncostatic drugs: study of modalities for pharmacodynamic potentiation.

Authors:  R Pouillart; T H Huong; E Brugerie; J Lheritier
Journal:  Biomedicine       Date:  1974-12-10

2.  Phase II study of mitomycin C and vinblastine in women with advanced breast cancer refractory to standard cytotoxic therapy.

Authors:  J M Denefrio; D R East; M B Troner; C L Vogel
Journal:  Cancer Treat Rep       Date:  1978-12

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

Authors:  R D Hart; M Perloff; J F Holland
Journal:  Cancer       Date:  1981-10-01       Impact factor: 6.860

Review 4.  The anthracycline antineoplastic drugs.

Authors:  R C Young; R F Ozols; C E Myers
Journal:  N Engl J Med       Date:  1981-07-16       Impact factor: 91.245

5.  Vinblastine, adriamycin, thiotepa, and halotestin (VATH): therapy for advanced breast cancer refractory to prior chemotherapy.

Authors:  M Perloff; R D Hart; J F Holland
Journal:  Cancer       Date:  1978-12       Impact factor: 6.860

6.  Treatment of advanced breast cancer with mitomycin C combined with vinblastine or vindesine.

Authors:  H S Garewal; R J Brooks; S E Jones; T P Miller
Journal:  J Clin Oncol       Date:  1983-12       Impact factor: 44.544

7.  Vinblastine given as a continuous 5-day infusion in the treatment of refractory advanced breast cancer.

Authors:  H Y Yap; G R Blumenschein; M J Keating; G N Hortobagyi; C K Tashima; T L Loo
Journal:  Cancer Treat Rep       Date:  1980 Feb-Mar

8.  Combination chemoimmunotherapy of metastatic breast cancer with 5-fluorouracil, adriamycin, cyclophosphamide, and BCG.

Authors:  G N Hortobagyi; J U Gutterman; G R Blumenschein; C K Tashima; M A Burgess; L Einhorn; A U Buzdar; S P Richman; E M Hersh
Journal:  Cancer       Date:  1979-04       Impact factor: 6.860

9.  Experience with the use of adriamycin in combination with other anticancer agents using a weekly schedule, with particular reference to lack of cardiac toxicity.

Authors:  A J Weiss; R W Manthel
Journal:  Cancer       Date:  1977-11       Impact factor: 6.860

10.  Doxorubicin, mitolactol (dibromodulcitol), and mitomycin C treatment for patients with metastatic breast cancer previously treated with cyclophosphamide, methotrexate, 5-FU, vincristine, and prednisone (CMFVP).

Authors:  A DiStefano; H Y Yap; G R Blumenschein
Journal:  Cancer Treat Rep       Date:  1981 Jan-Feb
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