Olaparib and Entinostat in Patients With Recurrent Platinum-Refractory Resistant Ovarian Primary Peritoneal Fallopian Tube Cancers

  • STATUS
    Recruiting
  • End date
    Sep 24, 2026
  • participants needed
    73
  • sponsor
    Vanderbilt-Ingram Cancer Center
Updated on 24 July 2021
ct scan
platelet count
cancer
hysterectomy
absolute neutrophil count
metastatic disease
serum pregnancy test
carcinoma
oophorectomy
MRI
metastasis
neutrophil count
liver metastasis
tumor cells
blood transfusion
follicle stimulating hormone
luteinizing hormone
entinostat
cancer chemotherapy
recurrent disease
olaparib
ovarian cancer
BRCA1
BRCA2
fallopian tube
platinum-based chemotherapy
endometrioid adenocarcinoma
clear cell adenocarcinoma
carcinosarcoma
serous adenocarcinoma
serous cystadenocarcinoma
cancer of the ovary

Summary

This phase I/II trial studies the side effects and best dose of olaparib and entinostat and to see how well they work in treating patients with ovarian, primary peritoneal, or fallopian tube cancers that have come back or do not respond to platinum-based chemotherapy. Olaparib and entinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Description

PRIMARY OBJECTIVES:

I. Determine the maximum tolerated dose (MTD) for the combination of olaparib and entinostat in the treatment of recurrent, platinum-refractory or resistant high-grade serous carcinoma of the ovary, fallopian tube or peritoneum. (Phase I) II. Determine the objective response rate in patients with recurrent, platinum-refractory or resistant, homologous repair proficient (HRP) high-grade carcinoma of the ovary, fallopian tube or peritoneum treated with the combination of olaparib and entinostat at the recommended phase 2 dose, as determined in phase I of this trial. (Phase II)

SECONDARY OBJECTIVES:

I. Assess the safety and tolerability of the combination of olaparib and entinostat in patients with recurrent, platinum-refractory or resistant high-grade serous carcinoma of the ovary, fallopian tube, or peritoneum. (Phase I) II. Further assess the nature and degree of toxicity of olaparib and entinostat in this cohort of patients. (Phase II) III. Determine the clinical benefit rate (CBR) (complete response [CR] + partial response [PR] + stable disease [SD]) as assessed at the time of best response to therapy). (Phase II) IV. Determine the progression free (PFS) and overall survival (OS). (Phase II) V. Determine the duration of response (DoR). (Phase II)

EXPLORATORY OBJECTIVES:

I. Assess the correlation between the Myriad myChoice homologous recombination pathway deficiency (HRD) score and the response to treatment.

II. Assess the degree of deoxyribonucleic acid (DNA) damage in circulating tumor cells and tumor biopsies (optional) after cycle 2 and at the end of treatment by phosphorylated (p)HAX2 and PAR and correlate with the response to treatment.

III. Assess baseline cyclin E amplification in ovarian tumors by fluorescence in situ hybridization (FISH) and correlate with response to treatment.

IV. Assess the expression of ki67/mib1 as a marker of cell proliferation in circulating tumor cells and in tumor biopsy specimens (optional) after cycle 2 of therapy and at the end of treatment and correlate with response to treatment.

V. Measure cyclin E1, CDK2, E2F1, and BRD expression by immunohistochemistry in circulating tumor cells and in tumor biopsy specimens (optional) after cycle 2 of therapy and at the end of treatment and correlate with response to treatment.

OUTLINE: This is a phase I, dose-escalation study followed by a phase II study.

Patients receive entinostat orally (PO) 1 week before starting combination therapy (day -7). Patients then receive entinostat PO on days 1, 8, 15, and 22, and olaparib PO twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression and unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days and then every 12 weeks.

Details
Condition Fallopian Tube Cancer, Recurrent Ovarian Carcinoma, Recurrent Primary Peritoneal Carcinoma, Fallopian Tube Clear Cell Adenocarcinoma, Fallopian Tube Endometrioid Adenocarcinoma, Ovarian Clear Cell Adenocarcinoma, Ovarian Endometrioid Adenocarcinoma, Primary Peritoneal Serous Adenocarcinoma, Recurrent Endometrial Cancer, Ovarian Carcinosarcoma, Recurrent Ovarian Cancer, High Grade Ovarian Serous Adenocarcinoma, High Grade Fallopian Tube Serous Adenocarcinoma, Fallopian Tube Carcinosarcoma, Recurrent Endometrial Carcinoma, fallopian tube cancers
Treatment olaparib, entinostat
Clinical Study IdentifierNCT03924245
SponsorVanderbilt-Ingram Cancer Center
Last Modified on24 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

High-grade carciomas of the ovary, fallopian tube, or periteonum, based on local pathology review, including high grade serous carcinoma, high grade endometrioid carcinomas, clear cell carcinoma, and carcinosarcoma
Platinum-refractory or resistant disease, as defined by progressive disease while receiving platinum-based chemotherapy or with recurrent disease < 6 months after the completion of platinum-based chemotherapy
May have received up to 2 prior therapies for platinum-resistant ovarian cancer
Must have received prior-platinum-based chemotherapy
BRCA1, BRCA2, RAD51, BRIP1, ATM, FANCL, PALB2 and other FA/BRCA pathway gene wild-type
Tumor HR-proficient, as assessed by Myriad myChoice HRD Test (HRD score < 42)
Provision of informed consent prior to any study specific procedures
Patients must have normal organ and bone marrow function measured within 28 days prior to administration of study treatment as defined below
Haemoglobin 10.0 g/dL with no blood transfusion in the past 28 days
Absolute neutrophil count (ANC) 1.5 x 109 /L
Platelet count 100 x 109 /L
Total bilirubin 1.5 x institutional upper limit of normal (ULN)
Aspartate aminotransferase (AST) (Serum Glutamic Oxaloacetic Transaminase (SGOT)) / Alanine aminotransferase (ALT) (Serum Glutamic Pyruvate Transaminase (SGPT)) 2.5 x institutional upper limit of normal unless liver metastases are present in which case they must be 5x ULN
Patients must have creatinine clearance estimated using the Cockcroft-Gault equation of 51 mL/min
Estimated creatinine clearance = (140-age [years]) x weight (kg) (x 0.85)
serum creatinine (mg/dL) x 72
Ideal body weight will be used, unless actual weight is less than ideal
Eastern Cooperative Oncology Group (ECOG) performance status 0-1
Patients must have a life expectancy 16 weeks
Amenorrheic for 1 year or more following cessation of exogenous hormonal treatments
Postmenopausal or evidence of non-childbearing status for women of childbearing potential: negative urine or serum pregnancy test within 28 days of study treatment and confirmed prior to treatment on day 1. Postmenopausal is defined
Luteinizing hormone (LH) and Follicle stimulating hormone (FSH) levels in the post menopausal range for women under 50
as
Radiation-induced oophorectomy with last menses >1 year ago
Chemotherapy-induced menopause with >1 year interval since last menses
Surgical sterilisation (bilateral oophorectomy or hysterectomy)
Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations
At least one lesion, not previously irradiated, that can be accurately measured at baseline as 10 mm in the longest diameter (except lymph nodes which must have short axis 15 mm) with computed tomography (CT) or magnetic resonance imaging (MRI) and which is suitable for accurate repeated measurements
The patient must provide separate informed consent to obtain the optional
Formalin fixed, paraffin embedded (FFPE) tumor sample or slides from the primary cancer must be available for myRisk HRD testing. If there is not written confirmation of the availability of an archived tumor sample prior to enrolment the patient is not eligible for the study. Additionally, a second FFPE tumor sample OR 10 unstained slides must be available for performance of correlative studies
tumor biopsy
If a patient declines to participate in the optional tissue biopsy, there will
be no penalty or loss of benefit to the patient. The patient will not be
excluded from other aspects of the study

Exclusion Criteria

Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site)
Previous enrollment in the present study
Participation in another clinical study with an investigational product during the last 4 weeks
Any previous treatment with PARP inhibitor, including olaparib
Any previous treatment with an HDAC inhibitor, including entinostat
Low grade or borderline epithelial ovarian, fallopian tube, or peritoneal cancers, sex- cord stromal tumors of the ovary, germ cell tumors of the ovary
Patients with known germline mutations of BRCA1, BRCA1, RAD51, ATM, FANCL, PALB2, and other FA/BRCA pathway genes
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), Stage 1, grade 1 endometrial carcinoma, or other solid tumours including lymphomas (without bone marrow involvement) curatively treated with no evidence of disease for 5 years. Patients with a history of localised triple negative breast cancer may be eligible, provided they completed their adjuvant chemotherapy more than three years prior to registration, and that the patient remains free of recurrent or metastatic disease
Resting ECG with QTcF > 470 msec on 2 or more time points within a 24 hour period or family history of long QT syndrome
Patients whose tumors are HR-deficient, as measured by Myriad myChoice HRD test
Patients receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) within 3 weeks prior to study treatment
Concomitant use of known strong CYP3A inhibitors (eg. itraconazole,telithromycin, clarithromycin, protease inhibitors boosted with ritonavir or cobicistat, indinavir, saquinavir, nelfinavir, boceprevir, telaprevir) or moderate CYP3A inhibitors (eg. ciprofloxacin, erythromycin, diltiazem, fluconazole,verapamil). See <https://secure.medicalletter.org/system/files/private/TML-article1491e.pdf> for a more complete list. The required washout period prior to starting olaparib is 2 weeks
If the first ECG shows QTcF > 470 msec, a second ECG within 24 hours would need to be completed
Concomitant use of known strong (eg. phenobarbital, enzalutamide, phenytoin, rifampicin, rifabutin, rifapentine, carbamazepine, nevirapine and St John's Wort ) or moderate CYP3A inducers (eg. bosentan, efavirenz, modafinil). See <https://secure.medicalletter.org/system/files/private/TML-article-1491e.pdf> for a more complete list. The required washout period prior to starting olaparib is 5 weeks for enzalutamide or phenobarbital and 3 weeks for other agents
Persistent toxicities (>Common Terminology Criteria for Adverse Event (CTCAE) grade 2) caused by previous cancer therapy, excluding alopecia
Patients with myelodysplastic syndrome/acute myeloid leukaemia or with features suggestive of MDS/AML
Patients with symptomatic uncontrolled brain metastases. A scan to confirm the absence of brain metastases is not required. The patient can receive a stable dose of corticosteroids before and during the study as long as these were started at least 4 weeks prior to treatment. Patients with spinal cord compression unless considered to have received definitive treatment for this and evidence of clinically stable disease for 28 days
Major surgery within 2 weeks of starting study treatment and patients must have recovered from any effects of any major surgery
Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3 months) myocardial infarction, uncontrolled hypertension, recent bleeding diathesis, uncontrolled major seizure disorder, unstable spinal cord compression, superior vena cava syndrome, extensive interstitial bilateral lung disease on High Resolution Computed Tomography (HRCT) scan or any psychiatric disorder that prohibits obtaining informed consent
Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication
Breast feeding women
Patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV)
Patients with a known hypersensitivity to olaparib or any of the excipients of the product
Patients with a known hypersensitivity to entinostat or any of the excipients of the product
Patients with known active hepatitis (i.e. Hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids
Previous allogenic bone marrow transplant or double umbilical cord blood transplantation (dUCBT)
Whole blood transfusions in the last 120 days prior to entry to the study
Patients taking warfarin
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