Status:

UNKNOWN

Functional Analysis of BRCAness

Lead Sponsor:

Leiden University Medical Center

Collaborating Sponsors:

Erasmus Medical Center

University Medical Center Groningen

Conditions:

Ovarian Neoplasm Epithelial

Homologous Recombination Deficiency

Eligibility:

FEMALE

18+ years

Phase:

PHASE2

Brief Summary

PARP inhibitors are most effective in homologous recombinant (HR) deficient tumors. There are clear indications that besides BRCA1 or BRCA2 mutated EOC, there is an additional group of EOC having defi...

Detailed Description

Epithelial ovarian cancer (EOC) often presents at an advanced stage, and harbours an unfavourable prognosis. Standard of care includes complete or optimal debulking surgery and chemotherapy, however, ...

Eligibility Criteria

Inclusion

  • Patients with recurrent high grade serous or endometrioid EOC (more than 3 months after platinum containing chemotherapy and unwilling or ineligible for platinum based therapy) with a tumor lesion that is amendable for biopsy or who can undergo ascites drainage prior to treatment.
  • Diagnosis of high grade serous or endometrioid EOC confirmed by histology .
  • Provision of informed consent prior to any study specific procedures
  • Female aged equal or above 18 years
  • Patients must have normal organ and bone marrow function measured within 28 days prior to administration olaparib
  • Eastern Cooperative Oncology Group performance status 0 to 2
  • Patients must have a life expectancy equal or above 16 weeks.
  • Postmenopausal or evidence of nonchildbearing 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.
  • Patients willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations.
  • Evaluable disease, measurable and, or nonmeasurable, that can be accurately assessed at baseline using RECIST by CT or MRI and is suitable for repeated assessment.
  • For inclusion in the optional exploratory genetic research and the optional biomarker research, patients must fulfil informed consent for genetic research and informed consent for biomarker research

Exclusion

  • Participation in another clinical study with an investigational product during the last month.
  • Any previous treatment with PARP inhibitor, including olaparib.
  • Other malignancy within the last 5 years, except, adequately treated nonmelanoma skin cancer, curatively treated in situ cancer, stage 1 and grade 1 endometrial carcinoma, or other solid tumours including breast cancer and lymphomas curatively treated with no evidence of disease for equal or above 3 years.
  • Patients receiving radiotherapy 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 equal or above grade 2, caused by previous cancer therapy, excluding alopecia.
  • Patients with symptomatic uncontrolled brain metastases. Patients with spinal cord compression unless considered to have received definitive treatment for this and evidence of clinically stable disease for 28 days.
  • Major surgery within 2 weeks of starting study treatment and patients must have recovered from any effects of any major surgery.
  • Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, nonmalignant systemic disease or active, uncontrolled infection.
  • Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication.
  • Breast feeding women.
  • Immunocompromised patients, for example, patients who are known to be serologically positive for human immunodeficiency virus.
  • Patients with a known hypersensitivity to olaparib or any of the excipients of the product.
  • Patients with known active hepatitis due to risk of transmitting the infection through blood or other body fluids
  • Previous allogenic bone marrow transplant or double umbilical cord blood transplantation.
  • Patients with myelodysplastic syndrome, acute myeloid leukaemia or with features suggestive of MDS, AML.
  • Whole blood transfusions in the last 120 days prior to entry to the study .
  • Resting ECG with QTc equal or above 470 msec on 2 or more time points within a 24 hour period or family history of long QT syndrome.

Key Trial Info

Start Date :

January 21 2019

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 21 2023

Estimated Enrollment :

55 Patients enrolled

Trial Details

Trial ID

NCT04780945

Start Date

January 21 2019

End Date

June 21 2023

Last Update

April 1 2021

Active Locations (3)

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Page 1 of 1 (3 locations)

1

University Medical Center Groningen

Groningen, Netherlands

2

Leiden University Medical Center

Leiden, Netherlands, 2300RC

3

Erasmus Medical Center

Rotterdam, Netherlands

Functional Analysis of BRCAness | DecenTrialz