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Observational Retrospective Study on Treatment and Outcomes in Patients With Low-grade Serous Ovarian Cancer

Observational Retrospective Study on Treatment and Outcomes in Patients With Low-grade Serous Ovarian Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02408536
Acronym
MITO 22
Enrollment
150
Registered
2015-04-03
Start date
2014-10-31
Completion date
2024-07-31
Last updated
2023-03-24

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

Conditions

Low-grade Serous Ovarian Carcinoma, Recurrent Invasive Borderline Serous Ovarian Cancer

Keywords

chemotherapy, hormone therapy, borderline, low-grade, serous ovarian cancer

Brief summary

The purpose of this study is to retrospectively evaluate treatments and outcomes of patients with low grade serous ovarian carcinomas in Italy.

Interventions

None listed

Sponsors

National Cancer Institute, Naples
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Diagnosis low-grade serous ovarian carcinoma * OR invasive recurrence after surgical resection of borderline serous ovarian carcinoma * Availability of archival tumor specimen (paraffin embedded block) for central analysis and evaluation for mutations * Age \> 18 years * Signed informed consent

Exclusion criteria

* High-grade serous, mucinous, endometrioid, or any other non-low-grade serous ovarian carcinoma * Unavailability of archival tumor specimen

Design outcomes

Primary

MeasureTime frame
number of patients with objective tumor response after receiving combination hormonal and chemotherapy6 months
risk of recurrence in patients with low-grade serous ovarian carcinomatwo years
number of patients with objective tumor response after receiving chemotherapy6 months
number of patients with objective tumor response after receiving hormone therapy6 months
progression free survival2 years
overall survival5 years

Countries

Italy

Contacts

Primary ContactFrancesco Perrone, MD PhD
datamanager@usc-intnapoli.net+39 081 5903571
Backup ContactTeresa Ribecco, PhD
teresa.ribecco@usc-intnapoli.net+39 081 5903619

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026