Olaparib Tablets as a Treatment for Ovarian Cancer Subjects With Different HRD Tumor Status

Relapsed Ovarian Cancer, BRCA Mutation, Platinum Sensitivity Clinical Trial

Official title:

Non-Randomized, Open-Label Phase II Study to Assess Olaparib Tablets as a Treatment for Subjects With Different HRD Tumor Status and With Platinum-Sensitive, Relapsed, High-Grade Serous or High-Grade Endometrioid Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer That Have Received at Least 1 Prior Line of Chemotherapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02983799
• Other study ID #: D0816L00003
• Status: Completed
• Phase: Phase 2
• Start date: December 22, 2016
• Est. completion date: December 3, 2020

Study information

• Verified date: March 2022
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a non-randomized, open-label study to assess olaparib tablets as a treatment for subjects with different homologous recombination deficiency (HRD) tumor status and with platinum-sensitive, relapsed, high-grade serous or high-grade endometrioid ovarian cancer. Subjects should have received at least 1 prior line of platinum-based chemotherapy.

Description:

This is a Phase II, open-label, non-randomized, multi-center study assessing the efficacy and safety of olaparib tablets 300 mg (two 150 mg tablets) given orally twice daily (bid) in subjects with platinum-sensitive or partially platinum-sensitive, relapsed, high-grade serous or high-grade endometrioid epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received at least 1 prior line of platinum-based chemotherapy.

The study will assess the effectiveness of olaparib tablets as measured by the objective response rate (ORR) as determined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1, in subjects with germline BRCA mutations (gBRCAm), somatic BRCA mutations (sBRCAm), or potential aberrations in homologous recombination deficiency (HRD) as determined by myChoice® HRD, as well as in subjects without identifiable HRD. This study will utilize Myriad BRACAnalysis CDx® for germline BRCA analysis and a tumor test (myChoice® HRD) for tumor BRCA analysis and HRD status. Four cohorts will be identified based upon the genetic testing described above:

• Cohort 1: gBRCAm,

• Cohort 2: sBRCAm and germline BRCA wild type,

• Cohort 3: myChoice® HRD positive (genomic instability positive) and BRCA wild type (BRCAwt) (no BRCA mutation),

• Cohort 4: myChoice® HRD negative (genomic instability negative) and BRCAwt (no BRCA mutation).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 272
• Est. completion date: December 3, 2020
• Est. primary completion date: December 3, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 130 Years

Eligibility

Inclusion Criteria:

• Provision of written signed informed consent prior to any study specific procedures;

• Female subjects with histologically diagnosed relapsed high-grade serous or high-grade endometrioid ovarian cancer;

• At least 1 lesion (measurable by RECIST v1.1) that can be accurately assessed at baseline by computed tomography (CT)/magnetic resonance imaging (MRI) and is suitable for repeated assessment;

• Subjects must have received at least 1 prior platinum-based line of chemotherapy for ovarian cancer. Note: There is no limit on the number of lines of chemotherapy;

• Subjects must be partially-platinum-sensitive (defined as progression 6 to 12 months after the end of the last platinum-based chemotherapy) or platinum sensitive (defined as progression > 12 months after the end of the last platinum-based chemotherapy);

• Subjects must have normal organ and bone marrow function measured within 28 days prior to administration of study treatment;

• ECOG performance status 0 to 1;

• Subjects must have a life expectancy greater than or equal to 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;

• Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations; and

• Formalin fixed, paraffin embedded tumor sample (either archival or fresh sample) from the primary or recurrent cancer must be available for central testing. If there is not written confirmation of the availability of an archived or fresh tumor sample prior to enrollment, the subject is not eligible for the study.

Exclusion Criteria:

• Involvement in the planning and/or conduct of the study (applies to both AstraZeneca Representative staff and/or staff at the study site);

• Previous enrollment in the present study;

• Exposure to any investigational product (IP) within 30 days or 5 half-lives (whichever is longer) prior to start of study treatment;

• Any previous treatment with a PARP inhibitor, including olaparib;

• Subjects who have platinum-resistant or refractory disease defined as progression during or within 6 months of the last platinum-based chemotherapy;

• Other malignancy within the last 5 years (few exceptions apply);

• Resting ECG with clinically significant abnormal findings;

• Subjects receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) within 3 weeks prior to study treatment;

• Concomitant use of known strong CYP3A inhibitors or moderate CYP3A inhibitors;

• Concomitant use of known strong or moderate CYP3A inducers;

• Persistent toxicities (> Common Terminology Criteria for Adverse Event [CTCAE] grade 2) caused by previous cancer therapy, excluding alopecia;

• Subjects with MDS/AML or with features suggestive of MDS/AML;

• Subjects with pneumonitis or at risk of pneumonitis;

• Subjects with symptomatic uncontrolled brain metastases;

• Major surgery within 2 weeks of starting study treatment, and subjects must have recovered from any effects of any major surgery;

• Subjects considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease, or active, uncontrolled infection;

• Breast feeding women;

• Immunocompromised subjects, e.g., subjects who are known to be serologically positive for human immunodeficiency virus;

• Subjects with known active hepatitis (i.e., Hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Ovarian Neoplasms
• Relapsed Ovarian Cancer, BRCA Mutation, Platinum Sensitivity

Intervention

Drug:
• OLAPARIB
300 mg olaparib tablets taken orally twice daily

Locations

Country	Name	City	State
Canada	Research Site	Edmonton	Alberta
Canada	Research Site	Halifax	Nova Scotia
Canada	Research Site	Hamilton	Ontario
Canada	Research Site	Kingston	Ontario
Canada	Research Site	Mississauga	Ontario
Canada	Research Site	Montreal	Quebec
Canada	Research Site	Montreal	Quebec
Canada	Research Site	Montreal	Quebec
Canada	Research Site	Sherbrooke	Quebec
Canada	Research Site	Toronto	Ontario
Canada	Research Site	Vancouver	British Columbia
Canada	Research Site	Winnipeg	Manitoba
United States	Research Site	Abington	Pennsylvania
United States	Research Site	Anchorage	Alaska
United States	Research Site	Annandale	Virginia
United States	Research Site	Aurora	Colorado
United States	Research Site	Berkeley Heights	New Jersey
United States	Research Site	Bronx	New York
United States	Research Site	Cincinnati	Ohio
United States	Research Site	Detroit	Michigan
United States	Research Site	Detroit	Michigan
United States	Research Site	Germantown	Tennessee
United States	Research Site	Hackensack	New Jersey
United States	Research Site	Hartford	Connecticut
United States	Research Site	Houston	Texas
United States	Research Site	La Jolla	California
United States	Research Site	Los Angeles	California
United States	Research Site	Milwaukee	Wisconsin
United States	Research Site	Minneapolis	Minnesota
United States	Research Site	New Haven	Connecticut
United States	Research Site	New York	New York
United States	Research Site	New York	New York
United States	Research Site	New York	New York
United States	Research Site	Newark	Delaware
United States	Research Site	Newark	New Jersey
United States	Research Site	Philadelphia	Pennsylvania
United States	Research Site	Pittsburgh	Pennsylvania
United States	Research Site	Portland	Oregon
United States	Research Site	Providence	Rhode Island
United States	Research Site	Saint Paul	Minnesota
United States	Research Site	Shreveport	Louisiana
United States	Research Site	Silver Spring	Maryland
United States	Research Site	Skokie	Illinois
United States	Research Site	South Miami	Florida
United States	Research Site	Springfield	Massachusetts
United States	Research Site	Teaneck	New Jersey
United States	Research Site	Winston-Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective Response Rate, Defined as the Percentage of Subjects With a Best Overall Response of Confirmed Complete Response (CR) or Partial Response (PR)	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using ORR according to RECIST v1.1 criteria (Investigator determined)	From first dose up until progression, or last evaluable assessment in the absence of progression (up to 36 months)
Secondary	Duration of Response, for Those Subjects With a Confirmed Response of CR or PR	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using duration of response	From the date of the measurement criteria for CR or PR are first met until the date of documented progression or death in the absence of disease progression (up to 36 months)
Secondary	CA-125 Response Rate, Defined as the Percentage of Subjects With a CA-125 Response According to GCIG Criteria Divided by the Number of Subjects Evaluable for CA-125 Response	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using CA-125 response rate	From baseline to Day 1 of each cycle and end of study treatment visit (up to 36 months)
Secondary	Disease Control Rate Defined as the Percentage of Subjects Who Have a Best Overall Response of CR or PR or SD at Greater Than or Equal to 8 Weeks Divided by the Number of Subjects in the Efficacy Analysis Set, Prior to Any PD Event	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using disease control rate (DCR). DCR is defined as the percentage of subjects with a best overall response of CR or PR (at any time up to and including the defined analysis cut-off point) or who have demonstrated stable disease (SD) for at least 8 weeks from first dose, divided by the number of subjects in the efficacy analysis set.	From first dose up until progression, or last evaluable assessment in the absence of progression
Secondary	Progression Free Survival	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using progression free survival	From first dose to earlier date of assessment of objective progression or death by any cause in the absence of progression (up to 36 months)
Secondary	Time to Any Progression	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using time to any progression	From first dose to earlier date of CA-125 progression or RECIST v1.1 progression, or death by any cause in absence of progression (up to 36 months)
Secondary	Overall Survival	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using overall survival	From date of first dose to date of death from any cause (up to 48 months)
Secondary	HRD Status as Per HRRm Gene Panel Assessment Will be Correlated With Clinical Outcome (ORR) for Subjects Enrolled in the 2 Cohorts With BRCAwt (Cohorts 3 and 4)	To determine the clinical effectiveness of olaparib treatment in each of 4 cohorts assessed using HRRm gene panel status related to clinical outcome	At baseline

External Links

•   Cancer Study Locator 1-877-400-4656 AstraZeneca@emergingmed.com
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