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FRAGINOC Study: The Impact of FRAilty Screening and Geriatric Assessment and Intervention in Older Patients With Epithelial Ovarian Cancer

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 70
Maximum Age: 120
Healthy Volunteers: f
View:

• Newly diagnosed ovarian cancer

• Capable of understanding written and oral danish

Locations
Other Locations
Denmark
Copenhagen University Hospital Rigshospitalet
RECRUITING
Copenhagen
Herlev and Gentofte Hospital
RECRUITING
Herlev
Odense University Hospital
RECRUITING
Odense
Zealand University Hospital
RECRUITING
Roskilde
Vejle Hospital
RECRUITING
Vejle
Contact Information
Primary
Tine Henrichsen Schnack, PhD
tine.henrichsen.schnack@rsyd.dk
+4527284828
Backup
Trine Lembrecht Joergensen, PhD
Trine.Joergensen@rsyd.dk
Time Frame
Start Date: 2023-02-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 300
Treatments
Active_comparator: NACT and CGA+ physical training intervention
Elderly (≥70 years) ovarian cancer patients referred for Neo-adjuvant treatment randomized to comprehensive geriatric assessment and individualised physical training.
No_intervention: NACT no intervention
Elderly (≥70 years) ovarian cancer patients referred for Neo-adjuvant treatment randomized to standard of care
Related Therapeutic Areas
Sponsors
Leads: Odense University Hospital
Collaborators: Zealand University Hospital, Herlev Hospital, Rigshospitalet, Denmark

This content was sourced from clinicaltrials.gov