Combining Fluzoparib and QL1101 for Maintenance in Advanced Ovarian Cancer

A Prospective, Single-Arm, Single-Center, Phase II Clinical Trial Evaluating the Efficacy and Safety of Fluzoparib Combined With QL1101 for Maintenance Treatment in Patients With Advanced Epithelial Ovarian Cancer Following Response After First-line Platinum-containing Chemotherapy

This study is testing if a combination of two drugs, Fluzoparib and QL1101, can help women with advanced ovarian cancer stay healthy longer after their initial chemotherapy.

Quick facts

• Phase: PHASE2
• Study type: Interventional
• Enrollment: 25 (estimated)
• Ages: 18 Years to 70 Years
• Sex: Female
• Sponsor: Liaoning Cancer Hospital & Institute (other)
• Drugs / interventions: chemotherapy, bevacizumab
• Locations: 1 site (Shenyang)
• Trial ID: NCT05585281 on ClinicalTrials.gov

What this trial studies

This study evaluates the effectiveness and safety of Fluzoparib combined with QL1101 as a maintenance treatment for patients with advanced ovarian cancer who have responded to initial platinum-based chemotherapy. It is a single-center, single-arm Phase 2 trial focusing on patients with high-grade serous or endometrioid ovarian cancer. Participants who achieve a complete or partial response after chemotherapy will receive Fluzoparib and QL1101 for up to two years, or until disease progression or other specified criteria are met.

Who should consider this trial

Good fit: Ideal candidates are women aged 18-70 with newly diagnosed, high-grade serous or endometrioid ovarian cancer who have responded to first-line platinum-based chemotherapy.

Not a fit: Patients with low-grade ovarian cancer or those who have not responded to initial chemotherapy may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could improve maintenance therapy options and outcomes for patients with advanced ovarian cancer.

How similar studies have performed: Other studies have shown promise in using maintenance therapies for ovarian cancer, but the specific combination of Fluzoparib and QL1101 is novel.

Eligibility criteria

Inclusion Criteria:

I-1.Patients voluntarily participated in this study and signed the informed consent.

I-2.Age 18-70 years, female. I-3.Eastern Cooperative Oncology Group (ECOG) performance status 0-1. I-4.Patients with newly diagnosed, histologically confirmed, high grade serous or high grade endometrioid ovarian cancer, fallopian-tube cancer, or primary peritoneal cancer（FIGO Stage III or IV）.

I-5.Completion of ideal tumor cytoreduction (either intermediate cytoreduction or initial cytoreduction).

I-6.First line therapy with platinum-taxane chemotherapy consists of a minimum of 6 treatment cycles and a maximum of 8 treatment cycles in patients who have achieved complete response (CR) or partial response (PR).

I-7.Patients who must receive at least 4 cycles of platinum-based therapy if non-hematologic toxicity specifically associated with platinum-based therapy (i.e., neurotoxicity, hypersensitivity reactions, etc.) necessitates early termination.

I-8.Those who can swallow tablets normally.

I-9.The functions of vital organs meet the following requirements:

1. Absolute neutrophil count ≥ 1.5 × 109/L;
2. Platelets ≥ 90 × 109/L;
3. Hemoglobin ≥ 100 g/L;
4. Serum albumin ≥ 30 g/L;
5. Bilirubin ≤ 1.5 × institutional upper limit of normal (ULN);
6. ALT and AST ≤ 3 × ULN; in case of liver metastases, ALT and AST \< 5 × ULN;
7. Serum creatinine ≤ 1.5 × ULN;
8. International normalized ratio (INR) ≤1.5 and activated prothrombin time (aptt) ≤1.5× ULN in patients not receiving anticoagulants.

I-10.Maintenance therapy is initiated within 8 weeks, counting from the last day of the last chemotherapy session, and all major toxicities from prior chemotherapy must be resolved by maintenance therapy to CTC Adverse Event grade 1 or better (except alopecia and peripheral neuropathy).

I-11.Normal blood pressure or adequately treated and controlled hypertension (systolic blood pressure ≤ 140 mmHg and/or diastolic blood pressure ≤ 90 mmHg) .

I-12.Willingness to undergo genetic testing: including germline and/or systemic BRCA1/2 testing, HRD testing, etc.

I-13.Non-surgical sterilization or female patients of childbearing age need to use two medically approved contraceptive measures (such as intrauterine devices, contraceptives or condoms) during the study treatment period and within 3 months after the end of the study treatment period; non-surgical sterilized female patients of childbearing age must have a negative serum human chorionic gonadotropin(HCG) test within 72 hours before the first dose, and must be non-lactating; for male patients whose partners are women of childbearing age, two effective methods of contraception should be used during the study treatment period and for 3 months after the end of the study treatment period.

Exclusion Criteria:

E-1.Non-epithelial origin of the ovary, the fallopian tube or the peritoneum (i.e. germ cell tumors).

E-2.Ovarian tumors of low malignant potential (e.g. borderline tumors), or mucinous carcinoma.

E-3.Clinical evidence of stable disease or progressive disease following treatment at the end of the first-line chemotherapy.

E-4.Other malignancy within the last 5 years except: adequately treated non-melanoma skin cancer curatively treated in situ cancer of the cervix, ductal carcinoma in situ (DCIS)Patients with a history of localized malignancy diagnosed over 5 years ago, who have completed all treatment and have no recurrent or metastatic disease prior to enrollment may be enrolled.

E-5.Patients with myelodysplastic syndrome/acute myeloid leukemia history. E-6.Patients receiving radiotherapy within 6 weeks or Major surgery within 4 weeks prior to study treatment.

E-7.Any previous treatment with PARP inhibitor, including fluzoparib. E-8.Prior history of hypertensive crisis (CTC-AE grade 4) or hypertensive encephalopathy.

E-9.Clinically significant (e.g. active) cardiovascular disease, including:

1. New York Heart Association (NYHA) grade 2 or higher heart failure.
2. Unstable angina pectoris.
3. Myocardial infarction within 1 year.
4. Clinically significant supraventricular or ventricular arrhythmia requiring treatment or intervention.
5. Qtc\>470ms. E-10.Patients who underwent cytoreductive surgery more than once before maintenance treatment（Patients who were considered unresectable at diagnosis only received biopsy or ovarian resection, and then continued chemotherapy for intermediate cytoreductive surgery may be enrolled）.

E-11.Patients who have received chemotherapy for abdominal or pelvic tumors, including those who received chemotherapy for early diagnosis of ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

E-12.Patients with synchronous primary endometrial cancer unless both of the following two criteria are met:

1. Sage \< 2.
2. Less than 60 years old at the time of diagnosis of endometrial cancer with stage ia or ib grade 1 or 2, or stage ia grade 3 endometrioid adenocarcinoma or ≥ 60 years old at the time of diagnosis of endometrial cancer with stage ia grade 1 or 2 endometrioid adenocarcinoma. Patients with serous or clear cell adenocarcinoma or carcinosarcoma of the endometrium are not eligible.

E-13.Pregnant or lactating women. E-14.Concomitant use of known potent CYP3A4 inhibitors such as ketoconazole, itraconazole, ritonavir, indinavir, saquinavir, telithromycin, clarithromycin, and nelfinavir.

E-15.History of allergic reactions to carboplatin. E-16.Participation in another clinical study with an investigational product.

Where this trial is running

Shenyang

• Yongpeng Wang — Shenyang, China (RECRUITING)

Study contacts

• Study coordinator: Yongpeng Wang

Conditions: Ovarian Cancer