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Frailty Evaluation in Elderly Population With Cancer (ELDERLY)

Primary Purpose

Fragility, Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Comprehensive Geriatric Assessment (CGA)
Sponsored by
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Fragility focused on measuring Elderly population with cancer, Toxicity risk, Mortality risk, Frailty conditions in elderly population, Chemotherapy in elderly population

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age more than 70 years
  • Outpatients
  • Patients diagnosed with stage III colon cancer, stage IV colorectal cancer or stage IV NSCLC
  • No previous diagnosis of cancer.
  • No previous chemotherapy for current diagnosis of cancer
  • Signed informed consent

Exclusion Criteria:

  • Not fulfilling inclusion criteria

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    CASE ARM

    CONTROL ARM

    Arm Description

    This is a three cohorts arm with intervention (CGA): Nutritional Assessment: Mini Nutritional Assessment (MNA) Functional Assessment: Get up and Go, Activities of Daily Living (ADL), Instrumental Activities of Daily Living (IADL), Karnofsky Scale, Walking one Block, Number of Falls in last 6 months and Hearing Loss. Cognitive Assessment: Mini-Mental State Examination (MMSE-30) Psychological status: Geriatric Depression Scale (GDS) Social Support: Medical Outcomes Study Social Support Survey (MOS-SSS) Comorbidity and Severity of Comorbidities: Charlson Comorbidity Index and Adult Comorbidity Evaluation (ACE-27) Age Haemoglobin Creatinine Clearance (CrCl) Presence of Geriatric Syndromes

    This is a three cohorts arm with no intervention

    Outcomes

    Primary Outcome Measures

    Number of participants with treatment related adverse events as assessed by CTCAE v4.0
    Evaluate occurrence of toxicity in both groups, experimental and control

    Secondary Outcome Measures

    Number of participants with occurrence of early mortality
    Evaluate occurrence of early mortality in both groups, experimental and control
    Number of Hospitalizations
    Evaluate occurrence of hospitalizations in both groups, experimental and control
    Number of participants with changes in cancer treatment related to toxicity
    Evaluate changes in treatment in both groups, experimental and control
    Number of participants with a change in therapeutic decision related to CGA
    Evaluate impact in the treatment for cancer in elderly population with NSCLC stage IV, colon cancer stage III and CRC stage IV of a CGA
    Contribution of different components of CGA to the management fo cancer
    Analysis of the weight of ech component through multiple regression
    Impact of CGA in health care in terms of human recourses and time consumption
    Cost of CGA measured in minutes for each component of CGA and person
    Predictive factors of events related to treatment
    To detect wich conditions predispose to adverse events

    Full Information

    First Posted
    March 17, 2017
    Last Updated
    May 26, 2017
    Sponsor
    Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
    Collaborators
    Hospital General Universitario Elche
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03101631
    Brief Title
    Frailty Evaluation in Elderly Population With Cancer
    Acronym
    ELDERLY
    Official Title
    Exploratory Study of Frailty Evaluation in Elderly Population With Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2, 2014 (Actual)
    Primary Completion Date
    July 30, 2014 (Actual)
    Study Completion Date
    January 30, 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
    Collaborators
    Hospital General Universitario Elche

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The Comprehensive Geriatric Assessment (CGA) is, still today, barely established in the standard practice. Although the different scientific societies recommend a CGA in elderly population affected with cancer at first visit, the evidence regarding its transcendence is limited. On the other hand, the components of this evaluation and the translation of their findings in changes in the clinical practice are not stablished. This project intends to implement a CGA in a group of patients to compare this group with an historical cohort that reflects the standard practice, to evaluate the differences between both approaches. The study also evaluate the feasibility and utility of this CGA. All these questions aims to support the hypothesis that CGA impacts on the cancer treatment for elderly population affected with cancer.
    Detailed Description
    This study compares two groups of elderly patients affected with stage IV non-small lung cancer (NSCLC), stage III colon cancer and stage IV colorectal cancer (CRC): a prospective experimental cohort and an historic control cohort. The sample size is 60 patients, 30 prospective and 30 retrospective. Of each cohort, 10 patients have stage IV NSCLC, 10 have stage III colon cancer and 10 have stage IV CRC. Prospective patients will be recruited longitudinally from January 2013 and retrospective patients are recorded longitudinally backward in time from December 2012. Both groups are patients of Medical Oncology Service of Hospital General Universitario de Elche, and both groups sign an informed consent form. A CGA is performed in the experimental group after the first visit with oncologist and prior to therapeutic decision. This CGA includes: Nutritional Assessment: Mini Nutritional Assessment (MNA) Functional Assessment: Get up and Go, Activities of Daily Living (ADL), Instrumental Activities of Daily Living (IADL), Karnofsky Scale, Walking one Block, Number of Falls in last 6 months and Hearing Loss. Cognitive Assessment: Mini-Mental State Examination (MMSE-30) Psychological status: Geriatric Depression Scale (GDS) Social Support: Medical Outcomes Study Social Support Survey (MOS-SSS) Comorbidity and Severity of Comorbidities: Charlson Comorbidity Index and Adult Comorbidity Evaluation (ACE-27) The evaluation includes too age, haemoglobin, Creatinine Clearance (CrCl) and presence of geriatric syndromes. The results of this evaluation allow to calculate: Early mortality risk according to Soubeyran et al (JCO 2012, 30: 1829-1834) (MNA and Get up and Go): risk of early mortality no risk of early mortality. Toxicity to chemotherapy according to Hurria et al. (J Clin Oncol 2011, 29: 3457-3465) (age, type of cancer, dose and number of chemotherapy drugs, haemoglobin, CrCl, hearing loss, number of falls in last 6 months, ability to take medication without help (IADL), walking one block and social support (MOS-SSS): low risk medium risk high risk. Frailty group according Köhne et al (The Oncologist 2008, 13: 390-402) (ADL, IADL, comorbidity and severity of comorbidities and presence of geriatric syndromes). This information dictates the therapeutic strategy for each experimental patient: Group 1: standard treatment. Group 2: modified treatment Group 3: no treatment Experimental patients will be followed for six months from CGA and their toxicity and its severity, occurrence of treatment modifications, number of hospitalizations and reasons for hospitalizations and mortality and reason of mortality will be compared with the same items of historic controls, followed too for six months from the moment the physician made the therapeutic decision. Other data to record for both groups: sex, age, origin, leucocytes, platelets, LDH, albumin, CEA, Cr Cl, haemoglobin, subjective weight loss, corporal mass index, comorbidities, primary tumor: stage, metastases location, treatment intent: adjuvant, palliative, number of drugs, number of concomitant medications, PS according to ECOG and Karnofsky (some data are expected to be missing for historic group). Only for historic controls, physicians should answer one question : In wich category would include the treatment recommendation? according to Köhne, The Oncologist 2008: Balducci, The Oncologist 2000; J Clin Oncol 2012: standard treatment modified treatment no treatment despite treatment is recommended no treatment Only for historic controls two more questions should be answered: Has a Geriatric Evaluation been performed? Yes or No What sort of evaluation? The trial records too how long does it take each test and how long does it take to complete CGA. All information is recorded in a database with anonymous code for each subject. Statistical analysis will consist of a descriptive analysis of sociodemographic and clinical characteristics of both cohorts. It will be performed also non-parametric analysis comparing this characteristics between the experimental groups. A descriptive analysis of daily life characteristics in experimental group will be performed, and also a non-parametric analysis comparing these variables between the experimental groups. Changes due to CGA incorporation will be evaluated and the variables measuring the toxicity and early mortality should be correlated to the coincidence or not of the treatment performed with the one concluded by the geriatric evaluation. Contribution of the different elements of CGA will be evaluated. A multiple regression will be performed in order to carry out an evaluation of the degree of contribution of each of the elements of the CGA. A significance "p" less than 0.05 will be considered significant. There are some study limitations: size, missing data for historic patients, monocentric study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fragility, Cancer
    Keywords
    Elderly population with cancer, Toxicity risk, Mortality risk, Frailty conditions in elderly population, Chemotherapy in elderly population

    7. Study Design

    Primary Purpose
    Screening
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Cases and Contols Study
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    62 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    CASE ARM
    Arm Type
    Experimental
    Arm Description
    This is a three cohorts arm with intervention (CGA): Nutritional Assessment: Mini Nutritional Assessment (MNA) Functional Assessment: Get up and Go, Activities of Daily Living (ADL), Instrumental Activities of Daily Living (IADL), Karnofsky Scale, Walking one Block, Number of Falls in last 6 months and Hearing Loss. Cognitive Assessment: Mini-Mental State Examination (MMSE-30) Psychological status: Geriatric Depression Scale (GDS) Social Support: Medical Outcomes Study Social Support Survey (MOS-SSS) Comorbidity and Severity of Comorbidities: Charlson Comorbidity Index and Adult Comorbidity Evaluation (ACE-27) Age Haemoglobin Creatinine Clearance (CrCl) Presence of Geriatric Syndromes
    Arm Title
    CONTROL ARM
    Arm Type
    No Intervention
    Arm Description
    This is a three cohorts arm with no intervention
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Comprehensive Geriatric Assessment (CGA)
    Other Intervention Name(s)
    Frailty Evaluation
    Intervention Description
    CGA includes a set of evaluations to determine therapeutic decision based on mortality risk, toxicity risk and frailty group. Evaluations includes: Nutritional Assessment: Mini Nutritional Assessment (MNA) Functional Assessment: Get up and Go, Activities of Daily Living (ADL), Instrumental Activities of Daily Living (IADL), Karnofsky Scale, Walking one Block, Number of Falls in last 6 months and Hearing Loss. Cognitive Assessment: Mini-Mental State Examination (MMSE-30) Psychological status: Geriatric Depression Scale (GDS) Social Support: Medical Outcomes Study Social Support Survey (MOS-SSS) Comorbidity and Severity of Comorbidities: Charlson Comorbidity Index and Adult Comorbidity Evaluation (ACE-27) Age Haemoglobin CrCl Presence of geriatric syndromes
    Primary Outcome Measure Information:
    Title
    Number of participants with treatment related adverse events as assessed by CTCAE v4.0
    Description
    Evaluate occurrence of toxicity in both groups, experimental and control
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Number of participants with occurrence of early mortality
    Description
    Evaluate occurrence of early mortality in both groups, experimental and control
    Time Frame
    6 months
    Title
    Number of Hospitalizations
    Description
    Evaluate occurrence of hospitalizations in both groups, experimental and control
    Time Frame
    6 months
    Title
    Number of participants with changes in cancer treatment related to toxicity
    Description
    Evaluate changes in treatment in both groups, experimental and control
    Time Frame
    6 months
    Title
    Number of participants with a change in therapeutic decision related to CGA
    Description
    Evaluate impact in the treatment for cancer in elderly population with NSCLC stage IV, colon cancer stage III and CRC stage IV of a CGA
    Time Frame
    6 months
    Title
    Contribution of different components of CGA to the management fo cancer
    Description
    Analysis of the weight of ech component through multiple regression
    Time Frame
    6 months
    Title
    Impact of CGA in health care in terms of human recourses and time consumption
    Description
    Cost of CGA measured in minutes for each component of CGA and person
    Time Frame
    Baseline
    Title
    Predictive factors of events related to treatment
    Description
    To detect wich conditions predispose to adverse events
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age more than 70 years Outpatients Patients diagnosed with stage III colon cancer, stage IV colorectal cancer or stage IV NSCLC No previous diagnosis of cancer. No previous chemotherapy for current diagnosis of cancer Signed informed consent Exclusion Criteria: Not fulfilling inclusion criteria
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Javier Gallego, PhD
    Organizational Affiliation
    HOSPITAL GENERAL UNIVERSITARIO DE ELCHE
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Links:
    URL
    http://meetinglibrary.asco.org/content/176401-195
    Description
    Poster
    URL
    http://meetinglibrary.asco.org/content/138955-158
    Description
    Poster

    Learn more about this trial

    Frailty Evaluation in Elderly Population With Cancer

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