OutCoME: Development of a Biomarker to Predict the Efficacy of Anti-angiogenic Therapy in Ovarian Cancer

Sponsor
Centro di Riferimento Oncologico - Aviano (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05874115
Collaborator
(none)
75
1
43.4
1.7

Study Details

Study Description

Brief Summary

Epithelial ovarian cancer (EOC) is a highly angiogenic tumor and drug targeting of angiogenesis is effective in some selected groups of EOC patients. However, no biomarkers are available to predict the effectiveness of this expensive therapy.Investigators believe that Multimerin-2, an extracellular matrix molecule, could serve as a biomarker that can address this clinical need. Multimerin-2 is deposited throughout the vasculature and its expression in EOC-associated vessels is frequently lost, in part due to increased degradation. Multimerin-2 sequesters VEGFA and other angiogenic factors and their release upon degradation of Multimerin-2 could underlie resistance to anti-angiogenic therapy. Indeed, fragments of degradation of Multimerin-2 are found in high concentrations in sera of EOC patients. Furthermore, the loss of Multimerin-2 impairs the function of the vessels, and this could negatively affect the delivery of the drug and the efficacy of the treatment.

With the aim of predicting the efficiency of anti-angiogenic therapy, researchers will evaluate the angiogenic properties and expression of Multimerin-2 in EOC tumors, and develop a new Multimerin-2-based biomarker detectable by liquid biopsy, in order to manage EOC patients in a targeted manner based on the biological characteristics of their tumor.

Condition or Disease Intervention/Treatment Phase
  • Other: liquid biopsy

Study Design

Study Type:
Observational
Actual Enrollment :
75 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Development of a Biomarker to Predict the Efficacy of Anti-angiogenic Therapy in Ovarian Cancer
Actual Study Start Date :
Oct 17, 2019
Anticipated Primary Completion Date :
May 31, 2023
Anticipated Study Completion Date :
May 31, 2023

Outcome Measures

Primary Outcome Measures

  1. Multimerin-2 levels and progression free survival [from EOC diagnosis diagnosis until first documented progression or death from any cause, up to 2 years]

    To investigate whether Multimerin-2 level measured in serum could represent a potential prognostic biomarker (measured as progression free survival) in bevacizumab-treated subjects

  2. Multimerin-2 levels and progression free survival [from EOC diagnosis diagnosis until first documented progression or death from any cause, up to 2 years]

    To investigate whether Multimerin-2 level measured in urine could represent a potential prognostic biomarker (measured as progression free survival) in bevacizumab-treated subjects

  3. Multimerin-2 levels and progression free survival [from EOC diagnosis diagnosis until first documented progression or death from any cause, up to 2 years]

    To investigate whether Multimerin-2 level measured in ascites could represent a potential prognostic biomarker (measured as progression free survival) in bevacizumab-treated subjects

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Female patients aged ≥18 years

  2. Histological diagnosis of epithelial carcinoma of the ovary or fallopian tubes or primary carcinoma of the peritoneum, including mixed Mullerian tumours.

  3. Stage IIIb, IIIc or IV

  4. Performance Status 0-2 according to ECOG

  5. Availability of tumor tissue samples and biological fluids for molecular analyses

  6. Informed consent for the collection, storage and use of biological material for the CRO Biobank (as specified in the consent of the CRO Biobank, Rev 2 of 03/10/2016), signed and obtained before surgery for suspected EOC.

Exclusion Criteria:
  1. Ovarian tumors of low malignant potential (i.e. borderline tumors)

  2. Other malignacies within the last 5 years except carcinoma in situ of the cervix or early stage squamous cell or basal cell carcinoma of the skin, as long as they are adequately treated.

  3. Active infection or uncontrolled chronic inflammatory disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centro di Riferimento Oncologico (CRO), IRCCS Aviano Italy

Sponsors and Collaborators

  • Centro di Riferimento Oncologico - Aviano

Investigators

  • Principal Investigator: Maurizio Maurizio, Centro di Riferimento Oncologico (CRO), IRCCS

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centro di Riferimento Oncologico - Aviano
ClinicalTrials.gov Identifier:
NCT05874115
Other Study ID Numbers:
  • CRO2019.053
First Posted:
May 24, 2023
Last Update Posted:
May 24, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2023