Efficacy of Platinum-based Chemotherapy in Platinum-resistant Ovarian Cancer) (EPITOC)

Last updated: August 12, 2019
Sponsor: Blokhin's Russian Cancer Research Center
Overall Status: Active - Not Recruiting

Phase

2/3

Condition

Chemotherapy

Vaginal Cancer

Pelvic Cancer

Treatment

N/A

Clinical Study ID

NCT04055038
PROC2019
  • Ages 18-70
  • Female

Study Summary

This is a phase II/III randomized controlled trial to evaluate efficacy of platinum-based chemotherapy vs conventionally prescribed non-platinum monochemotherapy in patients with platinum-resistant ovarian cancer

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

Total Participants: 164
Study Start date:
September 01, 2019
Estimated Completion Date:
January 01, 2022

Study Description

Recurrent ovarian cancer (ROC) is usually subdivided to platinum-sensitive (platinum-free interval [PFI] ≥6 mo.) and platinum-resistant ovarian cancer [PROC] (PFI <6 mo.) subtypes. Prognosis for the latter group is dismal and current guidelines recommend treating these patients with non-platinum based chemotherapy. However, the evidence behind this is quite unconvincing and according to recent data patients with non-platinum refractory platinum-resistant ovarian cancer could derive benefit from platinum rechallenge. This trial is designed for head-to-head comparison of platinum and non-platinum therapy efficacy in treatment of platinum-resistant ovarian cancer.

Connect with a study center

  • N.N. Blokhin Cancer Research Center

    Moscow, 115478
    Russian Federation

    Site Not Available

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