Efficacy and Safety of Niraparib Combined With Oral Etoposide in Platinum Resistant/Refractory Recurrent Ovarian Cancer

Ovarian Cancer Clinical Trial

Official title:

A Single Arm, Prospective, Multicenter, Phase II Study to Evaluate the Efficacy and Safety of Niraparib Combined With Oral Etoposide in Platinum Resistant/ Refractory Recurrent Ovarian Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04217798
• Other study ID #: CH1902001
• Status: Recruiting
• Phase: Phase 2
• Start date: May 21, 2020
• Est. completion date: June 1, 2022

Study information

• Verified date: December 2020
• Source: Peking Union Medical College Hospital
• Contact: Jiaxin Yang, MD
• Phone: 13661160998
• Email: yangjiaxin[@]pumch.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the efficacy and safety of niraparib combined with oral etoposide in platinum resistant or platinum refractory recurrent ovarian cancer.

Description:

This is a single arm, prospective, multicenter, phase II study to evaluate the efficacy and safety of PARP inhibitor niraparib combined with oral etoposide chemotherapy in women with platinum resistant or refractory recurrent ovarian cancer. Subjects will receive niraparib and oral etoposide in 30-day treatment cycles. After 6-8 cycles, oral etoposide will be discontinued. Subjects will receive niraparib alone until disease progression, intolerable toxicity or withdrawal of informed consent. The primary endpoint is progression free survival evaluated by Response Evaluation Criteria in Solid Tumors (RECIST v1.1). Secondary endpoints include overall response rate , duration of response, disease control rate, CA125 response rate and safety.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 36
• Est. completion date: June 1, 2022
• Est. primary completion date: March 1, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Signed informed consent before undertaking any study procedure.

• Female, age 18-70.

• Histologically confirmed FIGO stage III or IV non-mucinous epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

• No limitation of the BRCA mutation and HRD status.

• Platinum resistant or refractory recurrent disease.

• Subjects must have received at least 1 prior line of platinum-based chemotherapy regimen and no more than twice.

• Subjects must have measurable lesions with imaging evidence of disease progression (according to RECIST1.1 criteria); or without measurable/evaluable lesion (RECIST 1.1 criteria), but two consecutive cases of elevated CA125 > 2 times the upper limit of normal (> 70 U/ml) were detected.

• Life expectancy of more than 6 months.

• ECOG 0-1.

• Good organ function, including:

• Bone marrow function: neutrophil count =1,500/µL, platelets =100,000/µL, hemoglobin =10 g/dL;

• Hepatic function: total bilirubin = 1.5 x upper limit of normal (ULN) or direct bilirubin =1.0 x ULN, AST and ALT =2.5 x ULN unless liver metastases are present, in which case they must be =5 x ULN;

• Renal function: serum creatinine =1.5 x upper limit of normal (ULN) or calculated creatinine clearance =60 mL/min using the Cockcroft-Gault equation.

• Has a negative serum pregnancy test within 3 days prior to taking study treatment if of childbearing potential and agrees to abstain from activities that could result in pregnancy from screening through 3 months after the last dose of study treatment, or is of non-childbearing potential. Non-childbearing potential is defined as follows (by other than medical reasons):

• =45 years and <60 years of age and has not had menses for >1 year

• =60 years of age

• Post-hysterectomy, post-bilateral oophorectomy, or post-tubal ligation.

• Is able to adhere to the protocol.

• Has recovered from previous chemotherapy induced toxic side effects to = grade 1 CTCAE or basal level, apart from = grade 2 CTCAE peripheral neuropathy or hair loss symptoms at steady state.

Exclusion Criteria:

• Has a known hypersensitivity to the active or inactive ingredients of niraparib or compound which has similar chemical structure to niraparib.

• Has a known hypersensitivity to the active or inactive ingredients of etoposide or compound which has similar chemical structure to etoposide.

• prior PARP inhibitor therapy.

• Has symptomatic uncontrolled brain or leptomeningeal metastasis.

• Major surgery or chemotherapy within 3 weeks of starting the study or patient has not recovered from any effects of the surgery.

• Receive palliative radiotherapy encompassing > 20% of the bone marrow within 1 week of entering the study.

• Be diagnosed any invasive cancer other than ovarian cancer (apart from cured basal cell carcinoma and squamous cell carcinoma) within 2 years prior to study enrolment.

• Previously or currently diagnosed of myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML).

• Has other serious or uncontrolled disease.

• Has any disease, treatment and laboratory abnormality that may interfere the study results and affect the fully attendance of study. Or the subject is considered to be not suitable for the study by the investigator. Cannot receive platelet or red blood cell transfusion within 4 weeks of study drug administration.

• Pregnant, breastfeeding or expecting to conceive children during the study treatment period.

• Adjusted for QT interval (QTc) >470 msec.

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Drug:
• Niraparib
Subjects will receive niraparib combined with oral etoposide (on day 1-20, every 30 days). After 6-8 cycles, oral etoposide will be terminated. Niraparib will be still given to subjects until disease progression, intolerable toxicity or withdrawal of informed consent.

Locations

Country	Name	City	State
China	Peking Union Medical College Hospital	Beijing
China	Shandong Cancer Hospital	Jinan

Sponsors (2)

Lead Sponsor	Collaborator
Peking Union Medical College Hospital	Zai Lab (Shanghai) Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression Free Survival (PFS)	PFS is defined as the time from randomization to first disease progression by investigator assessment using RECIST 1.1 or death, from any cause, whichever comes first.	Through study completion, an average of 1 year
Secondary	Objective Response Rate (ORR)	ORR is defined as the proportion of subjects who have a partial response (PR) or complete response (CR) to therapy according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.	Through study completion, an average of 1 year
Secondary	Duration of Response (DOR)	DOR is defined as the time from the first date of response until the date of first documented progression.	Through study completion, an average of 1 year
Secondary	Disease Control Rate (DCR)	DCR is defined as the proportion of subjects who have a complete response (CR), partial response (PR) and stable disease (SD) to therapy according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.	Through study completion, an average of 1 year
Secondary	CA125 Response Rate	The proportion of subjects with a minimum 50% reduction in CA-125 serum levels lasting for =28 days relative to baseline CA-125 serum levels.	Through study completion, an average of 1 year
Secondary	The frequency and severity of adverse events	The frequency and severity of adverse events evaluated according to NCI CTCAE version 5.0 during subjects receiving the study treatment.	Through study completion, an average of 1 year