TY - JOUR
T1 - Phase II study of sequential hormonal therapy with anastrozole/exemestane in advanced and metastatic breast cancer
AU - Gebbia, Vittorio
AU - Pizza, null
AU - Formato, null
AU - Pappagallo, null
AU - Pisconti, Salvatore
AU - Pezzella, Giuseppe
AU - Quattrin, null
AU - Giotta, null
AU - Marzano, null
AU - Ferrari, null
AU - Incoronato, null
AU - Incoronato, null
AU - Cigolari, Silvio
AU - Pedicini, null
AU - Quattrin, null
AU - Febbraro, Antonio
AU - Incoronato, null
AU - Ianniello, Giovanni Pietro
AU - Tortoriello, null
AU - Caraglia, null
AU - Del Prete, Salvatore
AU - Iaffaioli, null
AU - Nasti, null
AU - Fanelli, null
AU - Colucci, null
AU - Manzione, Luigi
AU - Pisano, null
AU - Marano, null
PY - 2005
Y1 - 2005
N2 - Hormonal therapy is the preferred systemic treatment for recurrent or metastatic, post-menopausal hormone-receptor-positive breast cancer. Previous studies have shown that there is no cross-resistance between exemestane and reversible aromatase inhibitors. Exposure to hormonal therapy does not hamper later response to chemotherapy. Patients with locally advanced or metastatic, hormonal receptor positive or unknown, breast cancer were treated with oral anastrozole, until disease progression, followed by oral exemestane until new evidence of disease progression. The primary end point of the study was clinical benefit, defined as the sum of complete responses (CR), partial responses (PR) and > 24 weeks stable disease (SD). In all, 100 patients were enrolled in the study. Anastrozole produced eight CR and 19 PR for an overall response rate of 27% (95% CI: 18.6-36.8%). An additional 46 patients had long-term (> 24 weeks) SD for an overall clinical benefit of 73% (95% CI: 63.2-81.4). Median time to progression (TTP) was 11 months (95% CI: 10-12). A total of 50 patients were evaluated for the second-line treatment: exemestane produced one CR and three PR; 25 patients had SD which lasted ≥ 6 months in 18 patients. Median TTP was 5 months. Toxicity of treatment was low. Our study confirms that treatment with sequential hormonal agents can extend the period of time during which endocrine therapy can be used, thereby deferring the decision to use chemotherapy. © 2005 Cancer Research UK.
AB - Hormonal therapy is the preferred systemic treatment for recurrent or metastatic, post-menopausal hormone-receptor-positive breast cancer. Previous studies have shown that there is no cross-resistance between exemestane and reversible aromatase inhibitors. Exposure to hormonal therapy does not hamper later response to chemotherapy. Patients with locally advanced or metastatic, hormonal receptor positive or unknown, breast cancer were treated with oral anastrozole, until disease progression, followed by oral exemestane until new evidence of disease progression. The primary end point of the study was clinical benefit, defined as the sum of complete responses (CR), partial responses (PR) and > 24 weeks stable disease (SD). In all, 100 patients were enrolled in the study. Anastrozole produced eight CR and 19 PR for an overall response rate of 27% (95% CI: 18.6-36.8%). An additional 46 patients had long-term (> 24 weeks) SD for an overall clinical benefit of 73% (95% CI: 63.2-81.4). Median time to progression (TTP) was 11 months (95% CI: 10-12). A total of 50 patients were evaluated for the second-line treatment: exemestane produced one CR and three PR; 25 patients had SD which lasted ≥ 6 months in 18 patients. Median TTP was 5 months. Toxicity of treatment was low. Our study confirms that treatment with sequential hormonal agents can extend the period of time during which endocrine therapy can be used, thereby deferring the decision to use chemotherapy. © 2005 Cancer Research UK.
UR - http://hdl.handle.net/10447/16168
M3 - Article
SN - 0007-0920
VL - 92
SP - 1621
EP - 1625
JO - British Journal of Cancer
JF - British Journal of Cancer
ER -