RECRUITING

Decitabine and Selinexor in Combination to Reverse Drug Resistance With Standard Chemotherapy in Ovarian Cancer

Description

The goal of this clinical trial is to learn about the side effects and effectiveness of this novel four-drug combination of chemotherapy (decitabine, selinexor, carboplatin and paclitaxel) on patients with relapsed ovarian, fallopian or primary peritoneal carcinoma. Recently the investigators have found that the combination of decitabine and selinexor, two Food and Drug Administration (FDA) approved chemotherapy agents, may prevent or reverse the development of drug resistance and further the remissions and duration of remissions with standard ovarian cancer chemotherapy with carboplatin and paclitaxel. As decitabine and selinexor are not FDA approved for the participant's cancer, these agents are investigational.

Conditions

Ovarian Cancer
Talk to us

Related Conditions:

Ovarian Cancer

Study Overview

On this page

Study Details

Study overview

The goal of this clinical trial is to learn about the side effects and effectiveness of this novel four-drug combination of chemotherapy (decitabine, selinexor, carboplatin and paclitaxel) on patients with relapsed ovarian, fallopian or primary peritoneal carcinoma. Recently the investigators have found that the combination of decitabine and selinexor, two Food and Drug Administration (FDA) approved chemotherapy agents, may prevent or reverse the development of drug resistance and further the remissions and duration of remissions with standard ovarian cancer chemotherapy with carboplatin and paclitaxel. As decitabine and selinexor are not FDA approved for the participant's cancer, these agents are investigational.

Combination of the Hypomethylating Agent Decitabine and the Nuclear Export Receptor XPO-1 Inhibitor Selinexor to Reverse Platinum Resistance in Relapsed/Refractory Epithelial Ovarian Cancer

Decitabine and Selinexor in Combination to Reverse Drug Resistance With Standard Chemotherapy in Ovarian Cancer

Condition
Ovarian Cancer
Intervention / Treatment

-

Contacts and Locations

Maywood

Loyola University Medical Center, Maywood, Illinois, United States, 60153

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Participants must be greater than or equal to 18 years of age
  • * Participants must have an Eastern Cooperative Oncology Group (ECOG) Performance Status PS less than or equal to 2.
  • * Participants must have histological or cytological proven epithelial ovarian cancer, fallopian tube or primary peritoneal carcinoma with relapse or disease progression after prior treatment by exam, computed tomography (CT), PET/CT, or magnetic resonance imaging (MRI) may be enrolled. All cell types including clear cell carcinoma are eligible.
  • * Participants must have failed or relapsed after a platinum and taxane containing combination
  • * Participants must have adequate hepatic function
  • * Participants must have adequate renal function
  • * Participants must be able to swallow and retain oral medications
  • * Participants must have measurable disease according to Gynecologic Cancer Intergroup CA125 criteria
  • * Participants with stable (for 2 months or longer), treated (by radiotherapy) CNS metastases are eligible
  • * Participants with active hepatitis B virus (Hep B) are allowed if antiviral therapy for hepatitis B has been given for greater than 8 weeks.
  • * Participants must not have received Selinexor or another XPO1 inhibitor previously.
  • * Participants must not have had any concurrent medical condition or disease (eg, uncontrolled active hypertension, uncontrolled active diabetes, active systemic infection, etc.)
  • * Participants must not have uncontrolled active infection. Participants on prophylactic antibiotics or with a controlled infection within 1 week prior to C1D1 are acceptable.
  • * Participants must not have known intolerance, hypersensitivity, or contraindication to platinum or taxane therapy
  • * Participants must not have active, unstable cardiovascular function
  • * Participants must not have myocardial infarction within 3 months prior to starting
  • * Participants with untreated central nervous system (CNS) metastases are ineligible.
  • * Participants must not have had prior chemotherapy or radiation therapy
  • * Participants must not have DVT related to metastatic disease requiring ongoing anticoagulation.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Loyola University,

Patrick L Stiff, MD, PRINCIPAL_INVESTIGATOR, Loyola University

Study Record Dates

2031-08-28