Study on the Efficacy and Toxicity of Pamiparib Combined With Tamoxifen in the Treatment of Epithelial Ovarian Cancer Patients With Biochemical Recurrence During First-line PARPi Maintenance Therapy

Exclusion Criteria

• •1. Patients with other malignant tumors (except for patients with carcinoma in situ who have been fully treated and have no disease evidence, except for patients with thyroid cancer who have completed radical treatment, and patients with other malignant tumors who have completed radical treatment and have been screened for more than 5 years from the last tumor related treatment);
• •2. Imaging evaluation showed clear evidence of tumor recurrence or progression;
• •3. Pregnancy and perinatal patients;
• •4. Active pneumonia not cured;
• •5. History of important organ transplantation;
• •6. History of serious mental illness and brain dysfunction;
• •7. Drug abuse or drug abuse history;
• •8. Any active autoimmune disease or patient with a history of autoimmune disease (including but not limited to autoimmune hepatitis, interstitial pneumonia, hepatitis, enteritis, nephritis, hypophysitis, vasculitis, uveitis) or patients who need systemic hormone therapy and/or immunosuppression therapy (such as asthma requiring bronchodilators); Except for the following: vitiligo, alopecia, Graves syndrome, psoriasis or eczema that do not need systematic treatment in the past 2 years, stable immune thyroiditis that has been controlled after treatment, type I diabetes that only needs stable insulin, and childhood asthma has been completely alleviated;
• •9. The immunosuppressant or systemic hormone therapy is being used to achieve the purpose of immunosuppression (dose\>10mg/day prednisone or other equivalent hormone preparations), and it is still used 2 weeks before enrollment. Local and systemic use of prednisone or other equivalent hormone preparations not exceeding 10mg/day is allowed;
• •10. Patients with active bleeding (bleeding caused by tumor needs to be evaluated by the researcher), bleeding tendency or risk of massive bleeding (such as tumor involving large vessels, important bronchi, obvious bleeding beyond control after hemostasis treatment, and uncured bronchiectasis), or patients who need to be treated with coumarin anticoagulants at the same time;
• •11. Thrombosis or embolism events occurred in the past 6 months, such as cerebrovascular accident (including transient ischemic attack);
• •12. Serious cardiovascular disease or medical history includes but is not limited to the following:
• •* NYHA Grade 3 and 4 congestive heart failure within 6 months before enrollment
• •* Unstable angina or newly diagnosed angina or myocardial infarction within 12 months before screening
• •* Arrhythmias requiring treatment intervention (Patients with administration of β- receptor blockers or digoxin can be enrolled)
• •* Family history of prolonged QT interval syndrome or corrected QT interval (QTc)\>450ms; If the patient has an extended QTc interval, but the reason assessed by the investigator is that the pacemaker (and there is no other cardiac abnormality) is still included in the group
• •* CTCAE ≥ Grade 2 valvular heart disease
• •* Hypertension with poor control (systolic blood pressure\>150 mmHg or diastolic blood pressure\>100 mmHg;
• •13. Patients with moderate or above pulmonary dysfunction and unable to relieve them have interstitial lung disease or active pulmonary tuberculosis;
• •14. Patients with active ulcer, intestinal perforation, unresponsive intestinal obstruction, and patients with a history of gastrointestinal perforation within 28 days before inclusion in the study;
• •15. Active inflammatory bowel disease, uncontrollable nausea and vomiting, inability to swallow the study drug, and any gastrointestinal disease that may interfere with drug absorption and metabolism;
• •16. Active infections such as human immunodeficiency virus, syphilis, and untreated active hepatitis (HBV DNA copy number is greater than 1000 IU/ml, and HCV RNA is positive);
• •17. Serious infection occurred 4 weeks before the first administration;
• •18. Other serious or uncontrollable diseases, including but not limited to:
• •* Uncontrolled grand mal, unstable spinal cord compression, superior vena cava syndrome or other mental disorders that affect the patient's informed consent;
• •* Immune deficiency (excluding splenectomy), or other diseases that the researcher thinks may expose the patient to high risk toxicity;
• •* Those who have a history of abuse of psychotropic substances and are unable to quit or have mental disorders;
• •19. Inoculate live vaccine or attenuated live vaccine 30 days before the first administration;
• •20. Known allergy to active or inactive ingredients of the study drug or drugs with similar chemical structure; Patients who are pregnant or nursing, or who are expected to become pregnant during the study treatment;
• •21. Other laboratory inspection abnormalities:
• •* Uncorrectable hyponatremia (sodium\<130 mmol/L; serum potassium\<3.5 mmol/L)
• •* Any past or current disease, treatment or laboratory abnormality that may interfere with the results of the study and affect the patient's participation in the study, or the investigator believes that the patient is not suitable to participate in the study;
• •22. Any situation that the researcher thinks is not suitable for participating in the research, including poor understanding and low cooperation.