Niraparib and Bevacizumab Maintenance Therapy in Platinum-sensitive Recurrent Ovarian Cancer Patients Previously Treated With a PARP Inhibitor

Overview

This study is phase II, open label, clinical trial to determine the efficacy of Niraparib re-treatment with Bevacizumab of assessment progression-free survival(6 months PFS rate) with platinum-sensitive recurrent ovarian cancer patients previously treated with a PARP inhibitor.

Description

This is a Phase II, open-label, non-randomized, multi-center study assessing the efficacy and safety of Niraparib re-treatment with Bevacizumab of assessment progression-free survival(6 months PFS rate) with platinum-sensitive recurrent ovarian cancer patients previously treated with a PARP inhibitor The study will assess the effectiveness of progression-free survival(6 months PFS rate) as determined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. The subject will be treated to until disease progression as below:

• Niraparib 200mg or 300mg (once daily[QD])*
• Bevacizumab 15mg/kg every 3 weeks (Q3W)
• The recommended starting dosage of niraparib is 200mg QD. For patients who weigh ≥77 kg and have baseline platelet count ≥150,000/μL, the recommended starting dosage is 300 mg QD.

Eligibility

Inclusion Criteria:

1. Participant has histologically confirmed diagnosis of high-grade predominantly serous, endometrioid, carcinosarcoma, mixed mullerian with high-grade serous component, clear cell, or low-grade serous OC, primary peritoneal cancer, or fallopian tube cancer will be enrolled in this study (only up to 4 patients with clear cell carcinoma will be included and mucinous carcinoma will not be included).
2. Participant has received at least 2 previous courses of platinum-containing therapy, and has disease that was considered platinum sensitive following the penultimate (next to last) platinum course (more than 12 months' period between penultimate platinum regimen and progression of disease) Note: The last platinum regimen does not necessarily have to immediately follow the next to last (penultimate) platinum regimen. For example, if a patient received a non-platinum regimen between the penultimate platinum regimen and last platinum regimen, they could be eligible, so long as they meet all entry criteria.
3. Participant has responded to last the platinum regimen (complete or partial response), remains in response and is enrolled on study within 8 weeks of completion of the last platinum regimen
4. Participant had prior treatment with PARP inhibitor
5. Participant is able to provide a newly obtained core or excisional biopsy of a tumor lesion for prospective testing of BRCA 1/2 and PD-L1 status prior to enrollment
6. Female participants who are at least 20 years of age on the day of signing informed consent with
7. Participant has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, as assessed within 10 days prior to enrollment.

   Female participants:

8. A female participant is eligible to participate if she is not pregnant (see Appendix 2), not breastfeeding, and at least one of the following conditions applies:
   1. Not a woman of childbearing potential (WOCBP) as defined in Appendix 2 OR
   2. A WOCBP who agrees to follow the contraceptive guidance in Appendix 2 during the treatment period and for at least 120 days following the last dose of niraparib and at least 210 days following the last dose of chemotherapy or bevacizumab.

Informed Consent

          9. The participant (or legally acceptable representative if applicable) provides written
             informed consent for the trial. The participant may also provide consent for future
             biomedical research; however, the participant may participate in the main study
             without participating in future biomedical research.
         10. Participant has adequate organ function as defined in the following contents; all
             screening laboratory tests should be performed within 10 days prior to the start of
             study treatment.
               -  Absolute neutrophil count (ANC) ≥1500/µL
               -  Platelets ≥100 000/µL
               -  Hemoglobin ≥9.0 g/dL or ≥5.6 mmol/La
               -  Creatinine OR Measured or calculated creatinine clearance(GFR can also be used in
                  place of creatinine or CrCl) ≤1.5 × ULN OR ≥30 mL/min for participant with
                  creatinine levels >1.5 × institutional ULN
               -  Total bilirubin ≤1.5 ×ULN OR direct bilirubin ≤ULN for participants with total
                  bilirubin levels >1.5 × ULN
               -  AST (SGOT) and ALT (SGPT) ≤2.5 × ULN (≤5 × ULN for participants with liver
                  metastases)
               -  International normalized ratio (INR) OR prothrombin time (PT), Activated partial
                  thromboplastin time (aPTT) ≤1.5 × ULN unless participant is receiving
                  anticoagulant therapy as long as PT or aPTT is within therapeutic range of
                  intended use of anticoagulants
        Exclusion Criteria:
          1. Participant has mucinous, germ cell, or borderline tumor of the ovary.
          2. Participant has a history of non-infectious pneumonitis that required treatment with
             steroids or currently has pneumonitis
          3. Participant either has myelodysplastic syndrome (MDS)/ acute myeloid leukemia (AML) or
             has features suggestive of MDS/AML.
          4. Participant has a known additional malignancy that is progressing or has required
             active treatment within the past 2 years.
             Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of
             the skin, or carcinoma in situ (e.g. breast carcinoma, cervical cancer in situ,
             endometrial carinoma) that have undergone potentially curative therapy are not
             excluded.
             Note: Participants with synchronous primary endometrial cancer or a past history of
             primary endometrial cancer that met the following conditions are not excluded: Stage
             not greater than IA: no more than superficial myometrial invasion.
          5. Drainage of ascites during last 2 cycles of last chemotherapy.
          6. Palliative radiotherapy within 1 week encompassing >20% of the bone marrow.
          7. Persistent > grade 2 toxicity from prior cancer therapy.
          8. Symptomatic uncontrolled brain or leptomeningeal metastases. A scan to confirm the
             absence of brain metastases is not required. Patients with spinal cord compression may
             be considered if they have received definitive treatment for this and evidence of
             clinically stable disease for 28 days.
          9. Known hypersensitivity to the components of niraparib.
         10. Major surgery within 3 weeks of starting the study or patient has not recovered from
             any effects of any major surgery.
         11. Patients considered a poor medical risk due to a serious, uncontrolled medical
             disorder, non-malignant systemic disease or active, uncontrolled infection. Examples
             include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3
             months) myocardial infarction, uncontrolled major seizure disorder, unstable spinal
             cord compression, superior vena cava syndrome, or any psychiatric disorder that
             prohibits obtaining informed consent.
         12. History or current evidence of any condition, therapy, or lab abnormality that might
             confound the results of the study, interfere with the patient's participation for the
             full duration of the study treatment, or is not in the best interest of the patient to
             participate.
         13. Immunocompromised patients.
         14. Patients with known active hepatic disease (i.e. , Hepatitis B or C).