Assessment of the Efficacy and Safety of Olaparib Monotherapy Versus Physicians Choice Chemotherapy in the Treatment of Metastatic Breast Cancer Patients With Germline BRCA1/2 Mutations.



Status:Active, not recruiting
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 99
Updated:3/3/2019
Start Date:March 27, 2014
End Date:December 31, 2019

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A Phase III, Open Label, Randomised, Controlled, Multi-centre Study to Assess the Efficacy and Safety of Olaparib Monotherapy Versus Physicians Choice Chemotherapy in the Treatment of Metastatic Breast Cancer Patients With Germline BRCA1/2 Mutations.

This open label, randomised, controlled, multi-centre phase III study will assess the
efficacy and safety of single agent olaparib vs standard of care based on physician's choice
of capecitabine, vinorelbine or eribulin in metastatic breast cancer patients with gBRCA 1/2
mutations.


Inclusion Criteria:

- Germline mutation in BRCA1 or BRCA2 that is predicted to be deleterious or suspected
deleterious.

- Histologically or cytologically confirmed breast cancer with evidence of metastatic
disease.

- Prior therapy with an anthracycline and a taxane in either an adjuvant or metastatic
setting.

- Prior platinum allowed as long as no breast cancer progression occurred on treatment
or if given in adjuvant/neoadjuvant setting at least 12 months from last dose to study
entry elapsed.

- ER/PR breast cancer positive patients must have received and progressed on at least
one endocrine therapy (adjuvant or metastatic), or have disease that the treating
physician believes to be inappropriate for endocrine therapy.

- ECOG performance status 0-1.

- Adequate bone marrow, kidney and liver function.

Exclusion Criteria:

- Prior treatment with PARP inhibitor.

- Patients with HER2 positive disease.

- More than 2 prior lines of chemotherapy for metastatic breast cancer.

- Untreated and/or uncontrolled brain metastases.

- Prior malignancy unless curatively treated and disease-free for > 5 years prior to
study entry. Prior adequately treated non-melanoma skin cancer, in situ cancer of the
cervix, DCIS or stage I grade 1 endometrial cancer allowed.

- Known HIV (Human Immunodeficiency Virus) infection.

- Pregnant or breast-feeding women.
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