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NCT Number: NCT01742442

Cancer in the Elderly: Prevalence and Impact of Age Related Problems

About 50% of cancer patients are >70 years at diagnosis. Age related somatic and psychiatric problems may influence the course of cancer and its treatment. The present study is a prospective observational study. Age related problems will be assessed by clinical frailty indicators covering areas that are recommended in geriatric oncology. The aim is to describe the frequency of age related problems in a cohort of Norwegian cancer patients > 70 years of age, to investigate the predictive/prognostic impact of these indicators on cancer and treatment related morbidity and mortality, and to investigate the association between clinical frailty indicators, sarcopenia (severe loss of muscle mass) and inflammatory response. Patients are recruited at outpatient cancer services, Innlandet Hospital HF (SI), Oslo University Hospital, and Akershus University Hospital. Estimated sample size is 300 with 30 months inclusion and 2 years follow-up. The study emerges from SI in collaboration with several external national and international centres

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Key information

Conditions

Age range

70 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Akershus University Hospital, Lillestrøm, Lørenskog, Norway

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About this study

The proportion of elderly cancer patients is high and is likely to increase due to an increasing cancer incidence and an aging population. The prevalence and impact of age related problems are, however, poorly documented, and elderly patients may therefore be subjects to under-treatment and arbitrary modifications of treatment regimens. In order to improve clinical practice, precise identification of patients with increased vulnerability and risk of adverse outcomes is paramount.

In the present study, eligible patients will be identified by referral to oncology services at one of the participating cancer units. After consent, the baseline registrations will be performed including relevant medical and sociodemographic data, and quality of life. Age related problems will be assessed by clinical indicators covering comorbidity, medication, emotional, physical and cognitive function and nutritional status. Muscle mass will be quantified by analyses of diagnostic CT scans and a biobank will be established for the analyses of inflammatory markers. Upon inclusion, the patients' physician will be asked to rate the patients as fit, frail or intermediate according to the physicians' subjective judgement. The patients will be followed with assessments of quality of life, emotional function and nutritional status (self-report), cognitive and physical function (self-report and performance tests), muscle mass (diagnostic CT scans when available) and inflammatory markers (biobank). Follow up data will also include registry data (hospital records, primary health care registries, The Norwegian Patient Registry, The Norwegian Cancer Registry and the Norwegian Cause of Death registry). We will describe the prevalence of age related problems, investigate the relation between clinical frailty indicators, sarcopenia, inflammatory response and the physicians' subjective evaluation of the patients' health status. The predictive/prognostic impact of frailty indicators on the patients' self-reported physical function and quality of life, hospital and nursing home admittance, treatment toxicity and survival will also be investigated

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age >= 70 years
  • histologically/cytologically verified cancer disease
  • referred to specialist oncology service
  • no former chemotherapy for actual status (new cancer diagnosis no former or chemotherapy for metastatic disease)
  • subject to medical oncological treatment that may be initiated and administered at the hospital trust the patient is referred to
  • able to provide written consent
  • fluent in Norwegian (orally and written)

Exclusion criteria

  • lymphomas and haematological malignancies

Treatment and study plan

Primary outcomes

  1. Prevalence of age related problems

    Time frame: At baseline

    Age related problems assessed by clinical indicators including comorbidity, medication, emotional, physical, cognitive function, nutritional status and quality of life

  2. Physical decline

    Time frame: Follow-up

    Physical decline during follow-up, as measured by the EORTC QLQ-C30 questionnaire. We will investigate the predictive value of frailty (measured by clinical indicators), sarcopenia and inflammatory response on this outcome. Primary endpoint is defined as 2 months of follow-up

Secondary outcomes

  1. Hospital and nursing home admittance

    Time frame: 2-4 months and 2 years follow-up

    The predictive value of frailty indicators (including clinical indicators, sarcopenia and inflammatory response) on the outcome

  2. Quality of life

    Time frame: 2 - 4 months and 2 years follow-up

    The predictive impact of frailty indicators (including clinical indicators, sarcopenia and inflammatory response) on the outcome

  3. Treatment toxicity

    Time frame: 2-4months and up to 2 years

    The predictive impact of frailty indicators (including clinical indicators, sarcopenia and inflammatory response) on the outcome "treatment toxicity" defined in terms of any adverse event requiring hospital admission and haematological toxicity (grade 3-4 cytopenia). Toxicity during the first course of chemotherapy (2-3 weeks), during 3-4 courses (2-3 months) and for the whole follow-up. i.e. up to 2 years will be investigated

  4. survival

    Time frame: 2 years follow-up

    The prognostic value of frailty indicators (including clinical indicators, sarcopenia and inflammatory response on the outcome

Other outcomes

  1. The association between clinical frailty indicators, sarcopenia and inflammatory response

    Time frame: Baseline and 2 years follow-up

    Association between clinical frailty indicators, sarcopenia and inflammatory response

  2. The association between physicians' subjective evaluation of the patients' health status and clinical frailty indicators

    Time frame: Baseline and 2 years follow-up

    Agreement between physicians evaluation of health status and frailty based on a systematic assessment of frailty indicators

Sponsors and collaborators

Lead sponsor

Sykehuset Innlandet HF

Other

Collaborators

  • Diakonhjemmet Hospital
  • Oslo University Hospital
  • University of Alberta
  • Vestre Viken Hospital Trust

Registry information

Official study title

Cancer in the Elderly: Prevalence and Impact of Age Related Problems. A Prospective Observational Study

Important dates

Study start
2013
Primary completion
2015
Study completion
2017
First posted
Dec 5, 2012
Registry last updated
Apr 19, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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