HOVON HO34 MDS
Gearchiveerd
Main info
- Identificatie:
- HO34 MDS / EORTC 06961
- Sponsor:
- HOVON
- Active sites:
-
0(of 1)1 sites are pending
- Title:
Autologous Peripheral Blood Stem Cell Transplantation (PSCT) versus a second Intensive Consolidation Course after a Common Induction and Consolidation Course in Patients with bad prognosis Myelodysplatic Syndromes (MDS) and Acute Myelogenous Leukemia secondary (SAML) to MDS of more than 6 months duration: A Phase III Study.
Timeline
Scheduled
Actual
1996
15 dec.
Activated
1996
15 dec.
Activated
2006
15 dec.
Archived
2006
15 dec.
Archived
2010
27 mei
Closeout in Progress
2010
27 mei
Closeout in Progress
2025
27 mei
Destruction
2025
27 mei
Destruction
Flow
Details
- Phase:
- Prospective randomized Phase III study
- Monitoring Type:
- Objectives:
Eligibility
- Inclusion Criteria:
- All patients with untreated RAEBt, RAEB with > 10% blast cells in the bone marrow, other forms of MDS with multiple chromosomal abnormalities, and/or profound cytopenias, and secondary AML supervening after overt MDS of more than 6 months duration are eligible for the study.
- Patients between 10 and 60 years.
- Informed consent and expected cooperation of the patient with regard to treatment and follow-up.
- Performance status according to WHO: scale 0, 1 or 2.
- Exclusion Criteria:
- Blast crisis of chronic myeloid leukemia.
- Leukemias supervening after other myeloproliferative diseases.
- Leukemias supervening after overt MDS of less than 6 months duration.
- Inadequate renal and liver function.
- Patients with severe heart failure.
- Patients with severe concomitant neurological disease.
- Other progressive malignant diseases. However, secondary acute leukemias following cured Hodgkin�s disease or other malignancies will be included, as well as secondary leukemias following other exposure to alkylating agents or radiations for any other reason.
- Patients already treated for their MDS or AML by intensive chemotherapy, and/or radiotherapy.
- Patients treated with biological response modifiers and/or low dose Ara-C within 4 weeks prior to entry.
Participating Sites
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Site
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