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PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes. (PREDICTOR)

Primary Purpose

Myelodysplastic Syndromes

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
research of disease-related factors
research of comorbidities
physical performance
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Myelodysplastic Syndromes focused on measuring Hematology, Elderly, High Risk Myelodysplastic Syndrome

Eligibility Criteria

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

inclusion criteria:

  • Diagnosis of HR-MDS inferior to 6 weeks,
  • No treatment received before inclusion,
  • IPSS superior to 1 (intermediate 2 and high risk IPSS categories),
  • Social system affiliation,
  • Informed consent signed.

exclusion criteria:

  • Patient eligibility to stem cell transplantation,
  • IPSS inferior or egal 1 (low or intermediate 1 IPSS),
  • Concomitant investigational trial participation, which could interfere,
  • Patients under legal protection.

Sites / Locations

  • Hôpital Sud
  • Chu Angers
  • CH Annecy
  • CH Henri Duffaut
  • CH Blois
  • CH Boulogne sur mer
  • CH Sud Francillien
  • CHU Henri Mondor
  • CHU Albert Michallon
  • CH Versailles
  • CH du Mans
  • CH de Lens
  • Hôpital saint vincent de paul - Institut Catholique
  • CHU Limoges
  • Ch Lyon Sud
  • Institut Paoli Calmette
  • CH de Meaux
  • Chu Brabois
  • Chu Hotel Dieu
  • Hôpital de l'archet I
  • Hôpital COCHIN
  • Hôpital St Louis
  • CH Saint Jean
  • CHU Poitiers
  • CH René Dubos
  • Hôpital Pontchaillou
  • Centre Henri Becquerel
  • CH St Malo
  • CHU Toulouse
  • Hôpital Bretonneau
  • CH Princesse Grâce

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Evaluation of disease prognostic factors

Arm Description

Research of disease-related factors, research of comorbidities, geriatric assessment (Mini Mental Status Examination (MMSE), Geriatric Depression Scale-15, Mini Nutritional Assessment, Short Physical Performance Battery, grip strength, Fried criteria, Activities of Daily Living (ADL), Instrumental-ADL, G8, self-reported health status, quality of life Quality of Life Questionnaire-C30, Elderly Cancer Patients-14, EQ5D) at inclusion. At 3 months ADL and physical performance. Grade 3/4 toxicities and serious adverse events will be assessed during 6 months after inclusion (using NCI-COMMON TERMINOLOGY CRITERIA version 2.0) whatever treatment type (chemotherapy, supportive care).

Outcomes

Primary Outcome Measures

IPPS score

Secondary Outcome Measures

percentage of patients who had adverse events grade 3 or higher or having a serious adverse event
difference of geriatric assessment score between day 1 and 3 month

Full Information

First Posted
December 14, 2015
Last Updated
July 29, 2020
Sponsor
University Hospital, Toulouse
Collaborators
National Cancer Institute, France
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1. Study Identification

Unique Protocol Identification Number
NCT02689622
Brief Title
PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes.
Acronym
PREDICTOR
Official Title
Best PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 20, 2016 (Actual)
Primary Completion Date
January 31, 2019 (Actual)
Study Completion Date
January 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse
Collaborators
National Cancer Institute, France

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
No prospective study was conducted in elderly patients with cancer to assess the relative value of disease-related and patient-related prognosis factors. Patient-related prognostic factors have been highlighted in elderly patients with cancer resulting in the necessity of a geriatric assessment. The impact on overall survival of all of these factors was recognized in elderly people with cancer but remains unknown in High Risk Myelodysplastic Syndromes (HR-MDS). Therefore this information could be crucial to better select geriatric assessment domains relevant for the prediction and to recommend simplified tool after stratification of geriatric assessment domains thanks to their predictive value. The main hypothesis is that patient-related factors will have a better capacity to predict survival and treatment tolerance than disease-related factors in HR-MDS aged 75 and over and that the predictive value will be different among assessment tools which allows a selection of reduced number of tools for clinical use. To best knowledge estimation of predictive value of geriatric assessment tools remains unknown and explains why no standardization of practice exists. In testing all tools at the same cohort of patients allows to compare different tools and to define minimal and optimal geriatric assessment for HR-MDS. To determine the best strategy of geriatric assessment will allow in a second time to measure the impact of the use of this geriatric standardized evaluation by comparing patients'care and prognosis according to the use or not by the doctors of the new scores. Research outcomes are various medical, economic and ethic. Medical because decision-making will be improved with simplified geriatric assessment; economic because a better knowledge of geriatric assessment will improve treatment toxicity prevention and decrease treatment costs. Ethic will be associated with this project because a better knowledge of geriatric assessment tools to predict survival and tolerance treatment could improve the choice of best supportive care if prognosis markers are not favorable to active therapy. This project could induce important modification of practice in this area to an improved personalized treatment and simplification of geriatric assessment allowing a large diffusion in hospitals and clinics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myelodysplastic Syndromes
Keywords
Hematology, Elderly, High Risk Myelodysplastic Syndrome

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
157 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Evaluation of disease prognostic factors
Arm Type
Experimental
Arm Description
Research of disease-related factors, research of comorbidities, geriatric assessment (Mini Mental Status Examination (MMSE), Geriatric Depression Scale-15, Mini Nutritional Assessment, Short Physical Performance Battery, grip strength, Fried criteria, Activities of Daily Living (ADL), Instrumental-ADL, G8, self-reported health status, quality of life Quality of Life Questionnaire-C30, Elderly Cancer Patients-14, EQ5D) at inclusion. At 3 months ADL and physical performance. Grade 3/4 toxicities and serious adverse events will be assessed during 6 months after inclusion (using NCI-COMMON TERMINOLOGY CRITERIA version 2.0) whatever treatment type (chemotherapy, supportive care).
Intervention Type
Other
Intervention Name(s)
research of disease-related factors
Intervention Description
included in IPSS and IPSS-R, lactate dehydrogenase, ferritin level, transfusion- dependence, molecular markers as genes mutations
Intervention Type
Other
Intervention Name(s)
research of comorbidities
Intervention Description
HCT-Comorbidity Index, MDS-Comorbidity Index, Adult Comorbidity Evaluation-27, Cumulative Illness Rating Scale-G
Intervention Type
Other
Intervention Name(s)
physical performance
Intervention Description
Activities of Daily Living and physical performance
Primary Outcome Measure Information:
Title
IPPS score
Time Frame
1 year
Secondary Outcome Measure Information:
Title
percentage of patients who had adverse events grade 3 or higher or having a serious adverse event
Time Frame
6 months
Title
difference of geriatric assessment score between day 1 and 3 month
Time Frame
day 1 and 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
inclusion criteria: Diagnosis of HR-MDS inferior to 6 weeks, No treatment received before inclusion, IPSS superior to 1 (intermediate 2 and high risk IPSS categories), Social system affiliation, Informed consent signed. exclusion criteria: Patient eligibility to stem cell transplantation, IPSS inferior or egal 1 (low or intermediate 1 IPSS), Concomitant investigational trial participation, which could interfere, Patients under legal protection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Odile BEYNE-RAUZY, MD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Sud
City
Amiens
Country
France
Facility Name
Chu Angers
City
Angers
Country
France
Facility Name
CH Annecy
City
Annecy
Country
France
Facility Name
CH Henri Duffaut
City
Avignon
Country
France
Facility Name
CH Blois
City
Blois
Country
France
Facility Name
CH Boulogne sur mer
City
Boulogne Sur Mer
Country
France
Facility Name
CH Sud Francillien
City
Corbeil Essonnes
Country
France
Facility Name
CHU Henri Mondor
City
Creteil
Country
France
Facility Name
CHU Albert Michallon
City
Grenoble
Country
France
Facility Name
CH Versailles
City
Le Chesnay
Country
France
Facility Name
CH du Mans
City
Le Mans
Country
France
Facility Name
CH de Lens
City
Lens
Country
France
Facility Name
Hôpital saint vincent de paul - Institut Catholique
City
Lille
Country
France
Facility Name
CHU Limoges
City
Limoges
Country
France
Facility Name
Ch Lyon Sud
City
Lyon
Country
France
Facility Name
Institut Paoli Calmette
City
Marseille
Country
France
Facility Name
CH de Meaux
City
Meaux
Country
France
Facility Name
Chu Brabois
City
Nancy
Country
France
Facility Name
Chu Hotel Dieu
City
Nantes
Country
France
Facility Name
Hôpital de l'archet I
City
Nice
Country
France
Facility Name
Hôpital COCHIN
City
Paris
Country
France
Facility Name
Hôpital St Louis
City
Paris
Country
France
Facility Name
CH Saint Jean
City
Perpignan
Country
France
Facility Name
CHU Poitiers
City
Poitiers
Country
France
Facility Name
CH René Dubos
City
Pontoise
Country
France
Facility Name
Hôpital Pontchaillou
City
Rennes
Country
France
Facility Name
Centre Henri Becquerel
City
Rouen
Country
France
Facility Name
CH St Malo
City
Saint Malo
Country
France
Facility Name
CHU Toulouse
City
Toulouse
Country
France
Facility Name
Hôpital Bretonneau
City
Tours
Country
France
Facility Name
CH Princesse Grâce
City
Monaco
Country
Monaco

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes.

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