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

Ovarian Cancer Clinical Trial

— FRAGINOC  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05810701
• Other study ID #: OUHAgeCareOvarian
• Status: Recruiting
• Phase: N/A
• Start date: February 1, 2023
• Est. completion date: December 31, 2027

Study information

• Verified date: March 2023
• Source: Odense University Hospital
• Contact: Tine Henrichsen Schnack, PhD
• Phone: +4527284828
• Email: tine.henrichsen.schnack[@]rsyd.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Introduction Several studies have shown that a high percentage of patients with epithelial ovarian cancer (EOC) are undertreated due to their age, even in the absence of comorbidity. On the other hand, there seems to exist a group of frail patients unfit for extensive treatment that are over-treated. Therefore, it is of great interest to identify the group of older patients with EOC, who are frail and would benefit of a comprehensive geriatric assessment and optimisation, including individualised physical training. Unfortunately, no specific screening tool can be recommended or discouraged, and none of these tests are validated in patients with EOC. Immunodeficiency and biomarkers regarding nutritional status, strength, and general health are not part of the standard evaluation, although several studies have shown a correlation between these factors and the functional independence of older patients, comorbidity, postoperative complications, tolerance to chemotherapy and quality of life. In oncologic geriatrics a Comprehensive Geriatric Assessment (CGA - an examination performed by an interdisciplinary geriatric team) can be performed before start of treatment. Unfortunately, a complete CGA is both time and resource consuming, and the impact of interventions in older patients with EOC has never been examined. Hypothesis and purpose Our hypothesis is that frail patients with advanced ovarian cancer can benefit from a geriatric assessment and optimization, including physical training, increasing their chances of referral to surgery and to get full oncological treatment. The investigators believe that it is possible to develop a frailty screening tool with highly improved accuracy by combining known frailty screening tests, functional tests, and relevant biomarkers, which can help us select those patients who will benefit from a geriatric assessment and intervention. The clinical study is parceled out in two working projects, WP1 and WP2, which are anchored at the departments of gynecology, geriatric medicine, and oncology at several centers in Denmark. - WP1: Geriatric assessment and intervention and its impact on treatment outcomes examined in a cohort of older patients with EOC referred to NACT Primary endpoint: To determine whether a CGA and tailored intervention vs. standard of care can increase the proportion of patients referred to IDS. Secondary endpoints are a)to evaluate whether a CGA and tailored intervention can improve completion of chemotherapy, b) to investigate if CGA and a tailored intervention with physical training vs. standard of care improves treatment outcome and quality of life. - WP2: Impact of biomarkers, functional tests and immunological profile in assessing frailty and as predictors of adverse treatment outcomes in a national cohort of older EOC patients. Primary endpoint: to examine the performance of three validated frailty screening tests (G8, mG8, and Clinical Frailty Index (CFI)) in EOC patients in predicting impairments in CGA. Secondary endpoints are a)to examine whether adding functional tests, biomarkers, and the immunological profile can improve the accuracy of the frailty screening tests b) to examine whether the screening tool is predictive of patients achieving radical surgery and completing oncological treatment, as well as predict adverse treatment outcomes Method description The FRAGINOC project is a multicenter study, where WP1 is a clinical randomized trial of screening and intervention in older patients (≥70 years) with a diagnose of advanced EOC (FIGO stage III-IV). WP2 is a prospective observational study, where patients from WP1 will be asked to participate. Furthermore, older patients (≥70 years) referred to PDS or palliation will also be included. Patients will be evaluated at MDT conference, where they will be referred to either PDS and chemotherapy or NACT or palliation. Those referred to NACT will be re-evaluated at a second MDT conference after three cycles of chemotherapy to decide whether they can be referred to IDS. Screening All included patients will be screened for frailty after the MDT conference using a combination of the following tools: - Questionnaires (Geriatric-8, modified Geriatric-8 and clinical frailty scale). - Functional tests (hand grip test, 30 second chair test and 6 minutes walk test) - Blood samples, which have all been validated previously although in other cancer types. These tests will be repeated after the second MDT conference (after 3rd cycle of chemotherapy or before interval surgery) Randomization and Intervention After the initial frailty screening, patients eligible for primary chemotherapy will be randomized 1:1 to CGA and tailored intervention or standard of care. The intervention group will be evaluated by a geriatric specialist team examining different domains of their health status with the help of different validated questionnaires and tests, and tailored interventions will be made according to identified needs in the assessed health domains following the geriatric evaluation. The intervention will specifically include a tailored-made physiotherapy training program of around 9-12 weeks duration, available in both physical and virtual versions. The program consists on supervised resistance training two days a week, either at hospital appointments or virtually from the patients' own home. Those patients who are not able to make the virtual training will be followed up by phone twice a week by the physiotherapist. Additionally, the training will be supported by a progressive walking program measured with a Garmin Vivofit 4 activity tracker. Patients will be thoroughly assessed by a physiotherapist during the training process. Nutritional supplements and advice on sufficient nutrition will be provided according to current clinical guidelines. Patient-reported outcomes Measures (PROMs) All patients will be asked to complete the European Organization for Research and Treatment of Cancer's Quality of Life Questionnaire - Ovarian Cancer Module (EORTC QLQ C-30, QLQ-OV28) and the supplemental Elderly Cancer Patients Module questionnaire (ELD-14), as well as European Quality of Life- 5 dimensions- 5 levels questionnaire (EQ-5D-5L for cost-utility analysis, at inclusion, after three cycles of chemotherapy, and at the end of treatment. When assessing the quality of recovery, the QoR-15 questionnaire will be used and evaluated before surgery and 72 hours after PDS or IDS. Statistical plan/recruitment consideration According to the literature and clinical experience, increasing the number of patients who receive surgery from the present 57 % to 77 % is clinically relevant and possible. To detect a difference of 20 % and obtain a type I error rate of 5% and a power of 80%, a sample size of 86 patients per study arm will be needed. To account for an expected dropout rate of ~20%, it was decided to increase this number to a group size of 100. Thus, a total of 206 patients referred to NACT will be included in the study (WP1 only). Patients referred to PDS will be followed in an observational design. For the last three years, 130 patients fulfilling the inclusion criteria have been treated at RH, OUH, HUH, and SUH each year. Thus, inclusion is expected to run over 2-3 years. Data will be collected prospectively (demographic, clinical, pathologic, and results from frailty screening, functional tests, blood tests, and intervention effects), and recorded in predesigned RedCap. PRO will be completed by the patients either electronically and registered directly in RedCap, by phone calls or delivered in hand to the Ph.D. student or research nurses. Life-long follow-up data on overall survival will be obtained from the Danish Hospital Registry through linkage with a personal identification number. Logistic regression will be used to evaluate change over time in ordinal categorical values. Independent T-tests will be used to evaluate in-group and between-groups differences. Kaplan-Meier method and Cox regression analyses will be used to analyze Progression Free Survival.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: December 31, 2027
• Est. primary completion date: February 1, 2026
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 70 Years to 120 Years

Eligibility

Inclusion Criteria:

• Newly diagnosed ovarian cancer
• Capable of understanding written and oral danish

Exclusion Criteria:

• Other active cancers in the preceding 5 years
• Severe psychiatric disease Patients referred to primary debulking surgery will be followed in a observational design

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Frailty
• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Other:
• Comprehensive geriatric assessment and individualised physical training
Comprehensive geriatric assessment and relevant intervention (including medical and pharmacological optimisation, nutritional, social and psychological intervention, among others), and individualised physical training

Locations

Country	Name	City	State
Denmark	Copenhagen University Hospital Rigshospitalet	Copenhagen	The Capital Region Of Denmark
Denmark	Herlev and Gentofte Hospital	Herlev	The Capital Region Of Denmark
Denmark	Odense University Hospital	Odense	Region Of South Denmark
Denmark	Zealand University Hospital	Roskilde	Region Zealand
Denmark	Vejle Hospital	Vejle	Region Of South Denmark

Sponsors (4)

Lead Sponsor	Collaborator
Odense University Hospital	Herlev Hospital, Rigshospitalet, Denmark, Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Comprehensive Geriatric Assessment	Rate of number of intervened domains	Up to 8 months
Other	Hospital admissions related to chemotherapy	Rate of number and length of hospital admissions during chemotherapy treatment	Up to 8 months
Other	Physical activity in intervention group-walking	Median of daily distance in meters measured by an activity tracker	Up to 8 months
Other	Physical activity in intervention group-training	Rate of completion of training intervention	Up to 8 months
Other	Radicality of Surgery	Rate of optimal debulking vs suboptimal debulking during surgery	Up to 8 months
Other	Inflammatory biomarkers	Median of serum concentrations of inflammatory biomarkers (CRP, IL-6, YKL-40 and a panel of 92 proteins)	Up to 8 months
Other	Sarcopenic biomarkers	Median of serum concentrations of GDF-11 and GDF-15	Up to 8 months
Primary	Interval Debulking Surgery	Proportion of patients referred to interval debulking surgery	Up to 8 months
Primary	Frailty screening questionnaires	Specificity and positive and negative predictive values of Geriatric-8, modified Geriatric-8 and Clinical Frailty Scale, in predicting impairments in Comprehensive Geriatric assessment	Up to 8 months
Secondary	Completion of chemotherapy treatment	Proportion of patients who complete oncological treatment (=90% of the intended treatment)	Up to 8 months
Secondary	Effect of training: Physical capacity and endurance	Median of score result in meters of Six-Minute-Walk-Test	Up to 8 months
Secondary	Effect of training: Physical function and strength	Median of score result of 30 sec Sit-to-Stand Test in number (lower body) and of Hand Grip Strength test in Kg (upper body)	Up to 8 months
Secondary	Effect of physical training: Physical function in relation to basic mobility	Median of Timed Up and Go test in seconds	Up to 8 months
Secondary	Effect of physical training: Physical function in relation to balance	Median of Guralnik test: score in seconds	Up to 8 months
Secondary	Effect of physical training: Clinical reported measurements	Median of Performance status (number 0-4), Clinical Frailty Scale (1-9), G8 ( 0-17) and modified G8 (0-35)	Up to 8 months
Secondary	Effect of physical training: Self-reported measurements	Median of ELFI (0-100), Physical fitness (1-5) and FES-1 short (7-28)	Up to 8 months
Secondary	Patient-reported outcomes measures (PROMs)	Median of score of quality of life and recovery questionnaires	Up to 8 months
Secondary	Frailty screening combined tool	Specificity and positive and negative predictive values of a combination of Handgrip strength test, 30 second-chair stand test and 6 minutes walk tests, as well as serum concentrations of inflammatory biomarkers added to screening questionnaires (G8, mG8 and CFS), in predicting impairments in Comprehensive Geriatric assessment	Up to 8 months
Secondary	Postoperative complications	Median of score of Clavien-Dindo of complications within 30 days after surgery	Up to 8 months
Secondary	Progression Free-Survival	Median of period of time measured in months without recurrence of ovarian cancer	Up to 2 years