Advanced, recurrent epithelial ovarian cancer MedDRA version: 9.1 Level: LLT Classification code 10033160 Term: Ovarian epithelial cancer recurrent
Conditions
Sponsors
Onkologisk afdeling R and the Unit for Experimental Chemotherapy
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Histological verified epithelial carcinoma derived from ovarian, peritoneum or uterine tubes 2. Women =18 years old. 3. ECOG performance status =2 4. Expected duration of life >3 months. 5. Previous treatment regimen containing platinum and paclitaxel. 6. Platinum and paclitaxel sensitive tumor, defined as a minimum of 6 months from cessation of treatment until disease progression. 7. Measurable or assessable lesion. Patients having increased CA-125 as the only sign on recidive are also eligible. 8. Normal organ functions 9. Signed informed consent before inclusion. 10. Prepared to appear for the planned follow-up visits and capable of handling toxicity. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: 1. Patients treated with an experimental drug within the last 4 weeks before inclusion, and patients who receive other concomitant anticancer treatment. 2. Patients having an active infection, or who have received intravenous antibacterial or antifungal medicine within the last 2 weeks before inclusion. 3. Patients previously treated with an HDAC inhibitor. Patients, who have been treated with Valproate for convulsions can be included, however only if the treatment has taken place > 30 days before inclusion. 4. Patients treated with steroid, who are not stabilized on a firm dose equivalent to a maximum of 10 mg prednisolone per day for the last 4 weeks before inclusion. 5. Previous treatment with more than 1st line chemotherapy. 6. Progression during 1st line treatment regimen containing platin/paclitaxel or disease progression less than 6 months after treatment cessation. 7. Concomitant serious and/or non-controllable medical condition such as noncontrollable infection (including HIV infected patients), hypertension, ischemic heart disease, myocardial infarction within the last 6 months, congestive heart failure. 8. Previous treatment for, or other concomitant malignant disease within the last 5 years, except for curative treated carcinoma in situ cervical cancer or basal cell carcinoma. 9. Previous serious allergic reactions such as anaphylactic shock. 10. Pregnancy or breast feeding (or women within the childbearing age who are not using recognized contraception during the treatment and at least 3 months after treatment cessation). 11. Peripheral neuropathy = grade 2, unless this is due to a medical condition. 13. Patients with history of severe hyper sensitive reactions with regards to products containing Cremophor EL (cyclosporine or K-vitamin) and/or patients with known hypersensitivity towards compounds chemically connected to paclitaxel, carboplatin or vorinostat. 14. Clinical signs of cerebral metastases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: (1) To determine the objective response rate of patients with advanced, recurrent epithelial ovarian cancer, cancer of the Fallopian tube or primary peritoneal adenocarcinoma treated with paclitaxel plus carboplatin and vorinostat using conventional RECIST criteria.;Secondary Objective: (1) To assess the safety, tolerability, and adverse experience profile of vorinostat administered in combination with paclitaxel plus carboplatin. (2) To determine the progression-free survival (PFS) of patients with advanced, recurrent epithelial ovarian cancer, cancer of the Fallopian tube or primary peritoneal adenocarcinoma treated with paclitaxel plus carboplatin and vorinostat. ;Primary end point(s): | — |
Countries
Denmark
Outcome results
None listed