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Impact of Fas/FasL in Chemotherapy Response in Epithelial Ovarian Carcinoma

Impact of Fas/FasL in Chemotherapy Response in Epithelial Ovarian Carcinoma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02297958
Acronym
IFFaLCCO
Enrollment
28
Registered
2014-11-21
Start date
2015-01-15
Completion date
2019-07-27
Last updated
2020-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian Carcinoma

Brief summary

Ovarian carcinoma has poor prognosis and new therapeutic strategies are required. Many patients with ovarian carcinoma showed resistance to chemotherapy. Cleaved FasL is known for induced atypical response when is binding to Fas such as avoiding apoptosis and inducing cell motility.

Interventions

None listed

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Pre-Inclusion Criteria: \- Patient with suspicious ovarian carcinoma using clinical data, biological data (ca125) and radiological data (CT) Inclusion Criteria: * Pathological ovarian carcinoma diagnosed at pathological analysis after surgery. * Neo adjuvant chemotherapy

Exclusion criteria

* no neo-adjuvant chemotherapy * no ovarian carcinoma at final pathological analysis * less than 18 years old.

Design outcomes

Primary

MeasureTime frameDescription
Correlation between cleaved FasL level ans neoadjuvant chemotherapy tumor responsesurgeryMain outcome is cleaved FasL level and correlation with neoadjuvant chemotherapy tumor response, evaluated during surgery.

Secondary

MeasureTime frameDescription
Identification of tumoral T cellssurgeryIdentification of tumoral T cells with FACS analysis of dissociated tumor. Different T cells will be studies: Treg/Th17/Th1/Th2 using antibodies against: CD45/CD3/CD4/CD25/FOXP3 (Treg), CD45/CD3/CD4/IL17A (Th17), CD45/CD3/CD4/CD8/IL4/INF (TCD8 and LTCD4 Th1 et Th2).
Disease Free Survival rate18 months after surgery
Overall survival rate18 months after surgery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026