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Multicentre Study of Olaparib Maintenance Monotherapy in Platinum Sensitive Relapsed Non gBRCAm Ovarian Cancer Patients

CompletedPhase 3

Sponsor: AstraZeneca

Conditions: Non-Germline BRCA Mutated Ovarian Cancer

Interventions: Olaparib

Countries: Austria, Belgium, Bulgaria, Canada, Czechia, Denmark, Finland, Israel

The purpose of the study is to assess the efficacy and safety of single-agent olaparib as a maintenance treatment in patients with relapsed High Grade Serous Ovarian Cancer (including patients with primary peritoneal and/or fallopian tube cancer) or high grade endometrioid cancer who do not have known deleterious or suspected deleterious germline BRCA mutations (non-gBRCAm) and who had responded following platinum based chemotherapy

Eligibility overview

Sex: FEMALE

Age: 18 Years to 95 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Key Inclusion Criteria:

* Female patients with histologically diagnosed relapsed HGSOC (including primary peritoneal and / or fallopian tube cancer) or high grade endometrioid ovarian cancer
* Documented gBRCA1/2 mutation status
* Patients must have completed at least 2 previous courses of platinum containing therapy
* Patients must have normal organ and bone marrow function measured within 28 days of starting study treatment
* ECOG performance status 0-1 (see Appendix E)
* Patients must have a life expectancy ≥16 weeks
* Postmenopausal or evidence of non-childbearing status for women of childbearing potential: negative urine or serum pregnancy test within 28 days of study treatment and confirmed prior to treatment on day 1
* At least one lesion (measurable and/or non-measurable) that can be accurately assessed at baseline with computed tomography (CT) or magnetic resonance imaging (MRI) and is suitable for repeated assessment OR No evidence of disease following a complete response to chemotherapy
* An appropriately prepared tumour sample from the cancer, of sufficient quantity and quality (as specified in the Central Laboratory Services Manual) must be available for future central testing of tumour genetic status

Exclusion Criteria:

* Patients receiving any systemic hormonal therapy, chemotherapy or radiotherapy (except for palliative reasons) within 3 weeks prior to start of study treatment
* Any previous treatment with PARP inhibitor, including olaparib
* Patients with a germline BRCA mutation that is predicted to be deleterious or suspected deleterious (known or predicted to be detrimental / lead to loss of function)
* Other malignancy unless curatively treated with no evidence of disease for ≥5 years except: adequately treated non-melanoma skin cancer, curatively treated in situ cancer of the cervix, ductal carcinoma in situ (DCIS), Stage 1, grade 1 endometrial carcinoma.
* Concomitant use of known strong CYP3A inhibitors and strong (or moderate CYP3A inducers
* Persistent toxicities (≥ Grade 2 Common Terminology Criteria for Adverse Event (CTCAE) adverse event) caused by previous cancer therapy, excluding alopecia
* Patients with myelodysplastic syndrome (MDS)/acute myeloid leukaemia (AML) or with features suggestive of MDS/AML
* Patients with symptomatic uncontrolled brain metastases

Locations (91)

Graz, Austria
Innsbruck, Austria
Vienna, Austria
Wein, Austria
Brussels, Belgium
Leuven, Belgium
Loverval, Belgium
Namur, Belgium
Wilrijk, Belgium
Plovdiv, Bulgaria
Plovdiv, Bulgaria
Sofia, Bulgaria
Victoria, British Columbia, Canada
London, Ontario, Canada
Ottawa, Ontario, Canada
Toronto, Ontario, Canada
Montreal, Quebec, Canada
Sherbrooke, Quebec, Canada
Brno, Czechia
Nový Jičín, Czechia
Olomouc, Czechia
Ostrava, Czechia
Prague, Czechia
Aalborg, Denmark
Aarhus, Denmark
Kuopio, Finland
Oulu, Finland
Tampere, Finland
Afula, Israel
Beersheba, Israel
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