Everolimus in Combination With Exemestane in the Treatment of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer Who Are Refractory to Letrozole or Anastrozole



Status:Completed
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:June 2009
End Date:December 2014

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A Randomized Double-Blind, Placebo-Controlled Study of Everolimus in Combination With Exemestane in the Treatment of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer Who Are Refractory to Letrozole or Anastrozole

There are no treatments specifically approved after recurrence or progression on a non
steroidal aromatase inhibitors (NSAI). In light of the need for new treatment options for
postmenopausal women after failure of prior NSAI therapy, the purpose of this Phase III
study is to compare efficacy and safety of a treatment with exemestane + everolimus to
exemestane + placebo in postmenopausal women with estrogen receptor positive locally
advanced or metastatic breast cancer refractory to NSAI.


Inclusion Criteria:

- Adult women (≥ 18 years of age) with metastatic or locally advanced breast cancer not
amenable to curative treatment by surgery or radiotherapy.

- Histological or cytological confirmation of estrogen-receptor positive (ER+) breast
cancer

- Postmenopausal women.

- Disease refractory to non steroidal aromatase inhibitors (NSAI),

- Radiological or clinical evidence of recurrence or progression on or after the last
systemic therapy prior to randomization.

- Patients must have at least one lesion that can be accurately measured or bone
lesions in the absence of measurable disease as defined above.

Exclusion Criteria:

- HER2-overexpressing patients

- Patients with only non-measurable lesions other than bone metastasis (e.g. pleural
effusion, ascites etc.).

- Patients who received more than one chemotherapy line for Advanced Breast Cancer.

- Previous treatment with exemestane or mTOR inhibitors.

- Known hypersensitivity to mTOR inhibitors, e.g. sirolimus (rapamycin).

- Radiotherapy within four weeks prior to randomization

- Currently receiving hormone replacement therapy,

Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
64
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