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Activity of Exemestane in metastatic breast cancer after failure of nonsteroidal aromatase inhibitors : A Phase II Trial

Identifieur interne : 00C369 ( Main/Exploration ); précédent : 00C368; suivant : 00C370

Activity of Exemestane in metastatic breast cancer after failure of nonsteroidal aromatase inhibitors : A Phase II Trial

Auteurs : P. E. L Nning [Norvège, Italie, Australie, France, États-Unis, Argentine, Pays-Bas] ; E. Bajetta ; R. Murray ; M. Tubiana-Hulin ; P. D. Eisenberg ; E. Mickiewicz ; L. Celio ; P. Pitt ; M. Mita ; N. K. Aaronson ; C. Fowst ; A. Arkhipov ; E. Di Salle ; A. Polli ; G. Massimini

Source :

RBID : Pascal:00-0297144

Descripteurs français

English descriptors

Abstract

Purpose: To evaluate the antitumor activity and toxicity of a new steroidal aromatase inactivator, exemestane, in postmenopausal women with metastatic breast cancer who had progressive disease (PD) after treatment with a nonsteroidal aromatase inhibitor. Patients and Methods: In this phase II trial, eligible patients were treated with exemestane 25 mg daily (n = 241) followed, at the time PD was determined, by exemestane 100 mg daily (n = 58). Results: On the basis of the intent-to-treat analysis by independent review, exemestane 25 mg produced objective responses in 6.6% of patients (95% confidence interval [Cl], 3.8% to 10.6%) and overall success (complete response + partial response + no change for 24 weeks or longer) in 24.3% (95% Cl, 19.0% to 30.2%). The median durations of objective response and overall success were 58.4 weeks (95% Cl, 49.7 to 71.1 weeks) and 37.0 weeks (95% Cl, 35.0 to 39.4 weeks), respectively. increasing the dose of exemestane to 100 mg upon the development of PD produced one partial response (1.7%; 95% Cl, 0.0% to 9.2%). Both dosages were well tolerated and were discontinued because of adverse events in only 1.7% of patients. Conclusion: Exemestane 25 mg once daily seems to be an attractive alternative to chemotherapy for the treatment of patients with metastatic breast cancer after multiple hormonal therapies have failed.


Affiliations:


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Le document en format XML

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<title level="j" type="main">Journal of clinical oncology</title>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Androstane derivatives</term>
<term>Antineoplastic agent</term>
<term>Chemotherapy</term>
<term>Exemestane</term>
<term>Female</term>
<term>Human</term>
<term>Malignant tumor</term>
<term>Mammary gland</term>
<term>Metastasis</term>
<term>Negative therapeutic reaction</term>
<term>Phase II trial</term>
<term>Postmenopause</term>
<term>Toxicity</term>
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<term>Tumeur maligne</term>
<term>Glande mammaire</term>
<term>Femelle</term>
<term>Homme</term>
<term>Métastase</term>
<term>Essai clinique phase II</term>
<term>Exémestane</term>
<term>Toxicité</term>
<term>Anticancéreux</term>
<term>Postménopause</term>
<term>Chimiothérapie</term>
<term>Résistance traitement</term>
<term>Androstane dérivé</term>
<term>Hormonothérapie</term>
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<div type="abstract" xml:lang="en">Purpose: To evaluate the antitumor activity and toxicity of a new steroidal aromatase inactivator, exemestane, in postmenopausal women with metastatic breast cancer who had progressive disease (PD) after treatment with a nonsteroidal aromatase inhibitor. Patients and Methods: In this phase II trial, eligible patients were treated with exemestane 25 mg daily (n = 241) followed, at the time PD was determined, by exemestane 100 mg daily (n = 58). Results: On the basis of the intent-to-treat analysis by independent review, exemestane 25 mg produced objective responses in 6.6% of patients (95% confidence interval [Cl], 3.8% to 10.6%) and overall success (complete response + partial response + no change for 24 weeks or longer) in 24.3% (95% Cl, 19.0% to 30.2%). The median durations of objective response and overall success were 58.4 weeks (95% Cl, 49.7 to 71.1 weeks) and 37.0 weeks (95% Cl, 35.0 to 39.4 weeks), respectively. increasing the dose of exemestane to 100 mg upon the development of PD produced one partial response (1.7%; 95% Cl, 0.0% to 9.2%). Both dosages were well tolerated and were discontinued because of adverse events in only 1.7% of patients. Conclusion: Exemestane 25 mg once daily seems to be an attractive alternative to chemotherapy for the treatment of patients with metastatic breast cancer after multiple hormonal therapies have failed.</div>
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