Endometrial Cancer, Ovarian Cancer
Conditions
Keywords
LHRH receptor, receptor positive tumors, platinum resistant ovarian cancer
Brief summary
The purpose of this study is to determine whether AEZS-108 shows anti-tumor activity and is tolerated in patients with gynecological tumors (ovarian / endometrial cancer) that have been shown to express receptors for the luteinizing hormone releasing hormone (LHRH)
Detailed description
The ovary and the endometrium are hormone dependent organs. Receptors for different sex hormones are found commonly in epithelial ovarian and endometrial cancers. LHRH and its receptors are expressed in about 80% of human ovarian and endometrial cancers. As binding sites are present on tumors in higher concentrations than on most normal tissues, these receptors represent a specific target for AEZS-108 in which doxorubicin is coupled to an LHRH analog. Patients whose tumor specimen have shown to be positive for LHRH receptor expression will be investigated for tumor response and tolerability.
Interventions
DRUGAEZS-108
intravenous infusion at a dose of 267 mg/sqm every 3 weeks, up to 6 treatment cycles
Sponsors
AGO Study Group
AEterna Zentaris
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* LHRH receptor positive tumor status: positive receptor status determined by immunohistochemistry from primary tumor * Histologically confirmed epithelial ovarian cancer (Stratum A) * Advanced (FIGO III or IV) or recurrent disease * Progression during treatment with a platinum-based regimen or within 6 months after receiving a platinum-based regimen * Previous treatment with a taxane-containing regimen * At least one measurable target lesion (RECIST criteria) OR CA125 level higher than twice the upper limit of normal range (GCIG criteria) * Histologically confirmed endometrial cancer (Stratum B) * Advanced (FIGO III or IV) or recurrent disease not amenable to potentially curative treatment with local surgery and/or radiation therapy * No previous anthracycline-based chemotherapy * At least one measurable target lesion according to RECIST criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tumor response as per RECIST or (for Ovarian CA patients without evaluable target lesion following RECIST) GCIG criteria | up to six 3-weekly treatment cycles |
Secondary
| Measure | Time frame |
|---|---|
| Safety of AEZS-108 (possibly drug-related adverse events) | 4 weeks beyond last drug admnistration |
| Time-to-progression (TTP); Overall survival | up to observation of event |
Countries
Bulgaria, Germany
Outcome results
None listed