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Clinical Trials/NCT04478916
NCT04478916
Unknown
Not Applicable

Impact of the Comprehensive Geriatric Assessment on the Quality of Life of Elderly Onco-hematologic Patients' Candidates for Complex Antitumoral Therapies: Clinical and Biological Correlatives

Lorenza Scotti1 site in 1 country144 target enrollmentDecember 18, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hematologic Malignancies
Sponsor
Lorenza Scotti
Enrollment
144
Locations
1
Primary Endpoint
Number of patients received planned treatment and CGA evaluated with improvement of good quality of life (QOL)
Last Updated
5 years ago

Overview

Brief Summary

Impact of the Comprehensive Geriatric Assessment on the Quality of Life of elderly onco-hematologic patients' candidates for complex antitumoral therapies: clinical and biological correlatives

Detailed Description

The screenings for the next 2 decades indicate an exponential increase in the incidence of neoplastic diseases in the elderly population. In order to successfully balance effectiveness and low toxicity of immunochemotherapy, a treatment personalisation based on an objective evaluation of fitness is therefore needed. The use of geriatric screening is a first step to rationalize decisions in this regard, the G8 tool has demonstrated the ability to identify patients and mostly to objectively separate elderly fragile patients from those who are fit. In that consideration, the individualization of the anticancer treatment based on a Comprehensive Geriatric Assessment (CGA) is desirable in elderly fragile patients with solid or haematological malignancy. Cancer mortality is constantly increasing after 65 years and the consequent increase in life expectancy favour the processes of cellular senescence. In this context G8 fragility assessment will take place in the screening test and by using the EORTC QLQ-C30C questionnaire to assess quality of life (QoL). The evaluation of senescent cells will be done by real-time PCR. Our aims are i) to evaluate the impact of the CGA on the QoL of elderly onco-haematological patients, candidates for complex therapies, that resulted as fragile at the G8 geriatric screening and ii) to evaluate the senescent cells in the peripheral blood of the patients enrolled in the study. The study is expected to contribute to precision medicine management of elderly patients and refine the therapeutic stratifications.

Registry
clinicaltrials.gov
Start Date
December 18, 2019
End Date
May 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Lorenza Scotti
Responsible Party
Sponsor Investigator
Principal Investigator

Lorenza Scotti

Statistician

University of Eastern Piedmont

Eligibility Criteria

Inclusion Criteria

  • Patients aged ≥ 65 years
  • Diagnosis of solid or hematologic cancer
  • Patients who are candidates for a first line therapy for advanced disease to be treated with biological target drugs, or candidates for integrated radiotherapy
  • Patient with G8 scores ≤ 14/17

Exclusion Criteria

  • Patients aged less than 65 years
  • Patients who have received or currently in treatment for solid or hematologic cancer
  • Patient with G8 scores more than 14/17

Outcomes

Primary Outcomes

Number of patients received planned treatment and CGA evaluated with improvement of good quality of life (QOL)

Time Frame: 12 months after randomization (G8; at screening and every 6 months, QOL; at baseline and every 3 months, CGA; at baseline and every 6 months)

To assess the impact of the inclusion of the CGA on the quality of life (QOL) of the elderly onco-hematology patient that result frail in the geriatric screening (G8), compared to the clinical practice that does not include the CGA

Secondary Outcomes

  • Failure Free Survival (FFS)(From randomisation (December 2019-December 2022))
  • Number of patients received radiotherapy planned and CGA evaluated with improvement of good quality of life (QOL)(12 months after randomization (G8; at screening and every 6 months, QOL; at baseline and every 3 months, CGA; at baseline and every 6 months))
  • Progression free survival (PFS)(From randomisation (December 2019-December 2022))
  • Occurrence of dose reductions(From randomisation through study completion, an average of 1 year)
  • Overall Survival (OS)(From randomisation (December 2019-December 2022))

Study Sites (1)

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