Phase
Condition
Chemotherapy
Vaginal Cancer
Pelvic Cancer
Treatment
N/AClinical Study ID
Ages 18-70 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 18-70 years;
Histologically confirmed epithelial ovarian cancer (excluding mucinous, clear-cell andlow-grade subtypes);
Ovarian cancer recurrence within 3-6 months after completion of platinum-basedchemotherapy (given to possible variability in follow-up practices and tumor growthkinetics patients with platinum-free interval ≥3 and <7 months will be consideredplatinum-resistant);
Platinum-free interval ≤12 months;
Eastern Cooperative Oncology Group (ECOG) performance status ≤2;
Response to penultimate platinum-based chemotherapy defined as partial or completeresponse assessed by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1criteria or ≥50% reduction in CA-125 concentration for patients without measurablelesions;
Not refractory to penultimate platinum-based chemotherapy regimen (ie, the disease didnot progress during platinum-based chemotherapy and within ≤3 months after itscompletion);
Patients received ≤3 lines of prior chemotherapy;
No central nervous system (CNS) metastatic involvement;
No severe and uncontrolled concomitant diseases;
Adequate organ function:
Bone marrow - hemoglobin ≥ 90 g/l; Neutrophils ≥1,5x109/l; Platelets ≥75x109/l);
Renal - estimated creatinine clearance ≥50 ml/min (determined by Cockcroft-Gaultequation);
Hepatic - alanine aminotransferase (ALaT) & aspartate transaminase (ASaT) ≤3upper limit of normal (ULN), total bilirubin ≤ 25 umol/l;
Known BRCA1/2 mutation status as it will be used for stratification;
Life expectancy >3 months;
Patient is willingly consent to participate in the trial and signed informed consentform
Exclusion
Exclusion Criteria:
Platinum-refractory ovarian cancer defined as disease progression during penultimateplatinum-based chemotherapy or ≤3 month after its completion;
No response to penultimate platinum-based chemotherapy;
Mucinous, clear-cell or low-grade serous/endometrioid histology;
>3 lines of prior therapy lines for advanced ovarian cancer (prior maintenanceendocrine therapy or poly ADP ribose polymerase (PARP) inhibitors is allowed);
Prior therapy with PARP-inhibitors and endocrine therapy as a treatment forprogressive ovarian cancer;
Platinum-free interval >12 months;
Symptoms of bowel obstruction of any etiology;
Contraindications to platinum-based chemotherapy;
Planned administration of PARP inhibitors during or after this line of chemotherapy;
Life expectancy <3 months;
Uncontrolled and/or severe concomitant diseases (eg, uncontrolled diabetes mellitus,renal failure, hepatic failure, uncontrolled arterial hypertension, arrhythmia, heartfailure);
Metastatic CNS involvement;
Neuropathy grade >2.
Study Design
Study Description
Connect with a study center
N.N. Blokhin Cancer Research Center
Moscow, 115478
Russian FederationSite Not Available
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