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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02148731
Other study ID # ASRO101
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2010
Est. completion date December 2015

Study information

Verified date January 2019
Source Association Sud pour la Recherche en Oncogériatrie
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

MOST is a longitudinal study whose aim is to test the hypothesis that frailty markers are better at detecting vulnerable patients and that they are a better "Adverse Events" predictive tool than the CGA (Comprehensive Geriatric Assessment) in older cancer patients referred for chemotherapy. The second hypothesis is that a brief screening tool based on a combination of some frailty markers and some used in the CGA would help the oncologist detect patients requiring a more complete geriatric assessment


Description:

For older cancer patients, Comprehensive Geriatric Assessment (CGA) is recommended in order to help the oncologist in his decision making. However, the implementation of the CGA in oncologic setting presents major limitations; The CGA is time consuming, costly in terms of resources and is not standardized. Moreover, recent studies show that the CGA, used as the gold standard, may have a ceiling effect in detecting vulnerability in older cancer patients. Several authors suggest that a more sensitive approach, using frailty markers may be a better way to detect potential vulnerability in older cancer patients. In this study, for each patient, a brief screening assessment, a full CGA and the assessment of frailty markers will be completed at inclusion. The brief screening assessment will be based on self report questionnaire (4 items of instrumental Activities of Daily Living + 2 items of nutritional assessment) and one physical measure (one-leg standing balance test). The CGA will be based on seven domains (and their assessment tools): functional status, comorbidities, objective physical performance, nutrition, cognition, depression, and social support. Five frailty markers (as described by Fried and al) will be evaluated: nutrition, mobility, energy, physical activity and grip strength. CGA and frailty markers will be completed at 3, 6, 12 and 18 months after the beginning of chemotherapy as well as oncologic criteria (treatment toxicities, treatment modification such as decrease or change or end of chemotherapy, percentage of chemotherapy dose received, cancer related death) and geriatric criteria for adverse outcomes (functional, nutritional or cognition decline, hospitalization or consultation with their general practitioner, death for other causes).


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date December 2015
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria:

- Patients with colon cancer with or without metastases

- Age = 70 years

- Patients did not start chemotherapy yet

Exclusion Criteria:

- Patients terminally ill with a life expectancy <3 months

- Patients who have started chemotherapy or hormonal therapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Frailty markers
Brief screening assessment, CGA and frailty markers will be evaluate at inclusion. CGA and frailty markers will be evaluated at 3, 6, 12 and 18 months after the beginning of chemotherapy. Criteria for toxicity and adverse outcomes will be recorded at each cycle or visits

Locations

Country Name City State
France Hôpital d'Aix en Provence Aix en Provence
France Centre Hospitalier de la Dracénie Draguignan
France Hôpital Européen Marseille Marseille
France Institut Paoli Calmette Marseille
France Pôle de Gérontologie, Service de Gériatrie Aigue et Thérapeutique Nice
France Hôpital de Pontoise Centre Hospitalier René Dubos Pontoise, Val-d'Oise
France Centre Hospitalier Universitaire Intercommunal des Alpes du Sud Sisteron
France Centre Hospitalier Intercommunal Toulon

Sponsors (1)

Lead Sponsor Collaborator
Association Sud pour la Recherche en Oncogériatrie

Country where clinical trial is conducted

France, 

References & Publications (2)

Retornaz F, Monette J, Batist G, Monette M, Sourial N, Small D, Caplan S, Wan-Chow-Wah D, Puts MT, Bergman H. Usefulness of frailty markers in the assessment of the health and functional status of older cancer patients referred for chemotherapy: a pilot study. J Gerontol A Biol Sci Med Sci. 2008 May;63(5):518-22. — View Citation

Retornaz F, Seux V, Sourial N, Braud AC, Monette J, Bergman H, Soubeyrand J. Comparison of the health and functional status between older inpatients with and without cancer admitted to a geriatric/internal medicine unit. J Gerontol A Biol Sci Med Sci. 2007 Aug;62(8):917-22. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of Adverse Events The primary endpoint analysis is defined by the relationship between the CGA (Comprehensive Geriatric Assessment) and frailty markers on the one hand and the occurrence of adverse events on the other. The effect of each tool will be evaluated using a Cox model. The results will be adjusted on the main prognostic factors (age, type and stage of cancer). up to 18 months
Secondary Performance of the brief screening tool A second analysis will also evaluate the performance of the brief screening tool by determining its efficiency (specificity, sensitivity, positive and negative predictive values and accuracy) within the sample population in comparison to the CGA's and frailty markers. Estimations will be computed with a 95 % confidence interval. 3, 6, 12 and 18 months