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Am J Clin Oncol ; 11 Suppl 2: S112-4, 1988.
Article in English | MEDLINE | ID: mdl-2977263

ABSTRACT

From April 1984 to May 1986, 129 patients with prostate cancer entered a prospective trial with a new LH-RH agonist, Zoladex. Mean age was 72 years (range of 45-94 years) and, in most cases, patients had metastatic disease, not previously treated by chemotherapy or hormone therapy. Patients received a monthly injection of 3.6 mg. Serum testosterone was lowered into the range of castrate levels after 4 weeks of treatment. In 105 evaluable patients at 3 months, a 65% partial response (PR) rate was observed, with 11% stable and 24% progressive disease. Median time to progression was 37 weeks. Analysis of objective criteria revealed 30% PR for prostate volume and 51% CR-PR for prostatic acid phosphatases. Seventeen percent of lytic metastases had recalcified. One hundred twenty-nine patients were evaluable for toxicity. Endocrinological side effects were common: decrease in libido, 92%; impotence, 86%; hot flushes, 48%; and breast swelling or tenderness, 9%. Nonendocrinologic side effects were rare. The treatment is generally well accepted by patients owing to the convenient depot formulation and to the minor side effects.


Subject(s)
Buserelin/analogs & derivatives , Prostatic Neoplasms/drug therapy , Acid Phosphatase/analysis , Aged , Aged, 80 and over , Buserelin/administration & dosage , Buserelin/adverse effects , Buserelin/therapeutic use , Delayed-Action Preparations , Follicle Stimulating Hormone/blood , France , Goserelin , Humans , Injections, Subcutaneous , Luteinizing Hormone/blood , Male , Middle Aged , Multicenter Studies as Topic , Neoplasm Metastasis , Neoplasms, Hormone-Dependent/drug therapy , Neoplasms, Hormone-Dependent/enzymology , Prospective Studies , Prostate/enzymology , Prostatic Neoplasms/enzymology
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