Primary Outcome Measures: • To evaluate the efficacy of treatment with Azacitidine in patients with transfusion-dependent, low risk International Prognostic Scoring System (IPSS) 0 int-1, Myelodysplastic Syndrome (MDS) without chromosome 5 (5q) deletion. The main objective will be based on the erythroid haematologic response according to International Working Group (IWG) 2006 criteria. Secondary Outcome Measures: * Haematologic response, bases on the following parameters: platelets, and neutrophils according to International Working Group (IWG) Criteria. * Medullary and cytogenetic response according to International Working Group (IWG) 2006 criteria. * The effect of treatment response on quality of life, through the Functional Assessment of Cancer Therapy-Anemia (FACT-an) questionnaire. * Overall survival, Event-Free Survival and the Acute Leukaemia Transformation Rate.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Azacitidine 75 mg/m2, for 5 days of each 20 day cycle. Transfusional support will be applied for symptomatic anaemia using clinical discretion and chelation therapy when ferritin is ≥ 1000 μgr/ml with the chelating agents allowed
Hospital Reina Sofía, Servicio de Hematología
Córdoba, Cordoba, Spain
Hospital General de Jerez
Jerez de la Frontera, Cádiz, Spain
Hospital Universitario San Cecilio
Granada, Granada, Spain
Hospital Virgen de las Nieves
Granada, Granada, Spain
Hospital Juan Ramón Jiménez
Huelva, Huelva, Spain
Hospital Costa del Sol
Marbella, Malaga, Spain
Hospital Carlos Haya
Málaga, Malaga, Spain
Hospital Universitario Virgen del Rocío
Seville, Sevilla, Spain
Hospital Universitario Virgen de Valme
Seville, Sevilla, Spain
Erythroid haematologic response
To evaluate the efficacy of treatment with Azacitidine in patients with transfusion-dependent, low risk International Prognostic Scoring System (IPSS) 0 or int-1, Myelodysplastic Syndrome (MDS) without chromosome 5 (5q) deletion. The main objective will be based on the erythroid haematologic response according to International Working Group (IWG) 2006 criteria.
Time frame: Approximately the primary outcome is measured on days 0, 252 and 504 (basal, cycle 9 and 18 (each cicle has 28 days +/-3 days))
Haematologic response
Haematologic response, bases on the following parameters: platelets, and neutrophils according to International Working Group (IWG) Criteria.
Time frame: The secondary outcome is measured on days 0, 28, 56, 84, 112, 140, 168, 196, 224, 252, 280, 308, 336, 364, 392, 420, 448, 476 and 504 (the measurement is performed at basal line and in every cycle (every 28 days +/-3 days) up to a maximum of 18 cycles).
Medullary and cytogenetic response
Medullary and cytogenetic response according to International Working Group (IWG) 2006 criteria.
Time frame: Approximately this secondary outcome is measured on days 252 and 504 (basal, cycle 9 and 18 (each cicle has 28 days +/-3 days)).
Quality of life
The effect of treatment response on quality of life, through the Functional Assessment of Cancer Therapy-Anemia (FACT-An) questionnaire.
Time frame: Approximately this secondary outcome is measured on days 252 and 504 (basal, cycle 9 and 18 (each cicle has 28 days +/-3 days)).
Overall survival
Overall survival
Time frame: The secondary outcome is measured from basal line until day 504 (average of days for 18 cycles), or until progresion, or until exitus... (from basal line until the end of the study)
Event-Free Survival
Event-Free Survival
Time frame: The secondary outcome is measured from basal line until day 504 (average of days for 18 cycles), or until progresion, or until exitus... (from basal line until the end of the study)
Acute Leukaemia Transformation Rate
Acute Leukaemia Transformation Rate
Time frame: The secondary outcome is measured from basal line until day 504 (average of days for 18 cycles), or until progresion, or until exitus... (from basal line until the end of the study)
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