Abstract
In a randomised study 142 patients with advanced oestrogen-receptor-negative breast cancer in the tumour tissue received chemotherapy alone or chemotherapy combined with high doses (1000 mg daily) of oral medroxyprogesterone acetate (HD-MPA). Of the 126 fully evaluable for response, the response rates were 46% for chemotherapy alone and 73% for chemotherapy with HD-MPA (P = 0.005). There was no significant difference with regard to duration of response. Of the 138 patients evaluable for survival and toxicity, survival was shorter in the combined treatment group; median survival of 9 versus 13 months (P less than 0.05). Considerable toxicity was seen from HD-MPA, especially weight gain and fluid retention. The present study provides evidence that in concordance with preclinical studies an interaction between chemotherapy and HD-MPA may exist in breast cancer normally resistant to hormone therapy. The side-effects from MPA were substantial, however, and the survival data are of great concern.
Publication types
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Clinical Trial
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Multicenter Study
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Randomized Controlled Trial
MeSH terms
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Antineoplastic Agents / therapeutic use
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Breast Neoplasms / chemistry
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / mortality
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Cyclophosphamide / administration & dosage
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Doxorubicin / administration & dosage
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Female
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Fluorouracil / administration & dosage
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Humans
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Medroxyprogesterone / adverse effects
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Medroxyprogesterone / analogs & derivatives*
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Medroxyprogesterone / therapeutic use
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Medroxyprogesterone Acetate
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Middle Aged
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Mitomycins / administration & dosage
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Neoplasm Metastasis
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Neoplasm Proteins / analysis*
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Receptors, Estrogen / analysis*
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Vincristine / administration & dosage
Substances
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Antineoplastic Agents
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Mitomycins
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Neoplasm Proteins
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Receptors, Estrogen
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Vincristine
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Doxorubicin
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Cyclophosphamide
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Medroxyprogesterone Acetate
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Medroxyprogesterone
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Fluorouracil
Supplementary concepts
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CAV protocol
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FuMi protocol