PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes. (PREDICTOR)
Myelodysplastic Syndromes
About this trial
This is an interventional other trial for Myelodysplastic Syndromes focused on measuring Hematology, Elderly, High Risk Myelodysplastic Syndrome
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.
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
Experimental
Evaluation of disease prognostic factors
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).