Actively Recruiting

Phase Not Applicable
Age: 70Years - 120Years
FEMALE
NCT05810701

FRAGINOC Study: Screening and Geriatric Assessment and Intervention in Older Patients With Epithelial Ovarian Cancer

Led by Odense University Hospital · Updated on 2023-04-12

300

Participants Needed

5

Research Sites

256 weeks

Total Duration

On this page

Sponsors

O

Odense University Hospital

Lead Sponsor

R

Rigshospitalet, Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

Ovarian cancer (OC) is the fifth most common cause of cancer death. More than 40% are older than 70 years. The standard treatment is radical surgery combined with chemotherapy. More than 40% of the Danish patients will never undergo surgery. Frail and immunodeficient older patients are at higher risk of complications, and immunomodulating treatment as chemotherapy results in different outcomes in comparable patients. No accurate validated screening tool to identify frail and immunodeficient OC women exists. Optimization through comprehensive geriatric assessment (CGA) and physical training before and during treatment may improve outcomes and decrease associated risks. Aim: Primary endpoints will be to determine whether a CGA and physical training vs standard of care can increase the proportion of patients later on referred to interval debulking surgery, and examine the performance of validated screening tests in predicting impairments in CGA. Other endpoints will be to evaluate if intervention can improve completion of chemotherapy, to examine the association between frailty screening scores and selected biomarkers with treatment outcomes, including complications and quality of life, and ultimately to develop an improved frailty screening tool based on known screening tools, functional tests and biomarkers identifying patients who will benefit from CGA. Method: This is a nationwide, randomized intervention study. Patients ≥70 years diagnosed with primary OC at the Gynecological departments of Rigshospitalet, Odense and Roskilde University Hospitals will be included. In an interdisciplinary collaboration between medical specialists in oncology, gynecology and geriatrics, included patients will be screened for frailty using validated screening tools and functional tests. Specific biomarkers and immunologic profile will be assessed in all patients. Patients selected for neoadjuvant chemotherapy will be randomized to receive CGA or standard of care. Patients selected for primary debulking surgery or palliation will be followed in an observational cohort. Perspective: The development of a validated screening tool for frailty assessment and immunological status will help us identify frail patients who may need optimization before treatment, resulting in more patients getting optimal treatment (either surgery or chemotherapy), prevent post-treatment complications and avoid palliative patients from undergoing a redundant complex treatment.

CONDITIONS

Official Title

FRAGINOC Study: Screening and Geriatric Assessment and Intervention in Older Patients With Epithelial Ovarian Cancer

Who Can Participate

Age: 70Years - 120Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Newly diagnosed ovarian cancer
  • Able to understand written and spoken Danish
Not Eligible

You will not qualify if you...

  • Other active cancers within the past 5 years
  • Severe psychiatric disease

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Trial Site Locations

Total: 5 locations

1

Odense University Hospital

Odense, Region of South Denmark, Denmark, 5000

Actively Recruiting

2

Vejle Hospital

Vejle, Region of South Denmark, Denmark, 7100

Actively Recruiting

3

Zealand University Hospital

Roskilde, Region Sjælland, Denmark, 4000

Actively Recruiting

4

Copenhagen University Hospital Rigshospitalet

Copenhagen, The Capital Region of Denmark, Denmark, 2100

Actively Recruiting

5

Herlev and Gentofte Hospital

Herlev, The Capital Region of Denmark, Denmark, 2730

Actively Recruiting

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Research Team

T

Tine Henrichsen Schnack, PhD

CONTACT

T

Trine Lembrecht Joergensen, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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