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

NCT04055038UNKNOWNPHASE2, PHASE3INTERVENTIONAL

Summary

Key Facts

Lead Sponsor

Blokhin's Russian Cancer Research Center

Enrollment

164

Start Date

2019-09-01

Completion Date

2021-09-01

Study Type

INTERVENTIONAL

Official Title

Randomized Phase II/III Trial to Assess the Efficacy of Platinum-based Chemotherapy vs Standard Non-platinum Therapy in Patients With Platinum-resistant Recurrent Ovarian Cancer (ROC)

Interventions

Platinum-Based DrugConventional chemotherapy

Conditions

Ovarian CancerOvarian NeoplasmsSerous AdenocarcinomaBRCA1 MutationBRCA2 MutationChemotherapy

Eligibility

Age Range

18 Years – 70 Years

Sex

FEMALE

Inclusion Criteria:

* Age 18-70 years;
* Histologically confirmed epithelial ovarian cancer (excluding mucinous, clear-cell and low-grade subtypes);
* Ovarian cancer recurrence within 3-6 months after completion of platinum-based chemotherapy (given to possible variability in follow-up practices and tumor growth kinetics patients with platinum-free interval ≥3 and \<7 months will be considered platinum-resistant);
* Platinum-free interval ≤12 months;
* Eastern Cooperative Oncology Group (ECOG) performance status ≤2;
* Response to penultimate platinum-based chemotherapy defined as partial or complete response assessed by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria or ≥50% reduction in CA-125 concentration for patients without measurable lesions;
* Not refractory to penultimate platinum-based chemotherapy regimen (ie, the disease did not progress during platinum-based chemotherapy and within ≤3 months after its completion);
* 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-Gault equation);
  * Hepatic - alanine aminotransferase (ALaT) \& aspartate transaminase (ASaT) ≤3 upper 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 consent form

Exclusion Criteria:

* Platinum-refractory ovarian cancer defined as disease progression during penultimate platinum-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 maintenance endocrine therapy or poly ADP ribose polymerase (PARP) inhibitors is allowed);
* Prior therapy with PARP-inhibitors and endocrine therapy as a treatment for progressive 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, heart failure);
* Metastatic CNS involvement;
* Neuropathy grade \>2.

Outcome Measures

Primary Outcomes

Objective response rate (RR) according to RECIST 1.1 criteria

Primary outcome for Phase II part: response rate to treatment according to RECIST1.1 criteria. For patients without measurable disease Rustin criteria is allowed.

Time frame: 0-18 weeks

Overall survival defined as time from randomization to death from any reason;

Primary outcome for Phase III part: 2. Overall survival defined as time from randomization to death from any reason

Time frame: 1 year

Secondary Outcomes

Progression-free survival

Progression-free survival (PFS) defined as time from randomization to disease progression according to RECIST 1.1 criteria or death from any reason;

Time frame: 12 months

Overall survival

Overall survival defined as time from randomization to death from any reason (for Phase II part only);

Time frame: 12 months

Progression-free survival 2 (PFS2)

PFS2 defined as time from randomization to second disease progression event according to RECIST 1.1 criteria or death from any reason;

Time frame: 24 months

Objective response rate (RR) according to RECIST 1.1 criteria

Response rate to treatment according to RECIST1.1 criteria. For patients without measurable disease Rustin criteria is allowed (only for Phase II part).

Time frame: 12 months

Locations

N.N. Blokhin Cancer Research Center, Moscow, Russia

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