Trial | NCT00047268  Report issue

Title

Donor Stem Cell Transplant With or Without Chemotherapy in Treating Children With Primary Myelodysplastic Syndrome
Prospective Study of the Diagnosis and Treatment of Myelodysplastic Syndromes (MDS) in Childhood

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Unknown status

  • Study Participants

    None
RATIONALE: Giving chemotherapy before a donor stem cell transplant helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. It is not yet known whether donor stem cell transplant is more effective with or without chemotherapy in treating primary myelodysplastic syndrome.

PURPOSE: This phase III trial is studying how well donor stem cell transplant given with chemotherapy works and compares it with donor stem cell transplant without chemotherapy in treating children with primary myelodysplastic syndrome.
OBJECTIVES:

Determine, by a standard approach, the frequency of different FAB subtypes in children with primary myelodysplastic syndromes.
Determine the frequency of cytogenetic and molecular abnormalities in these patients.
Determine the survival of patients treated with allogeneic stem cell transplantation with or without induction chemotherapy.
Determine the rate of complete remission in patients treated with these regimens.
Determine the event-free survival of patients treated with these regimens.
Determine the relapse rate, morbidity, and mortality of patients treated with these regimens.
Determine different subsets of patients who benefit from these regimens.

OUTLINE: This is a multicenter study. Patients are stratified according to FAB subtype (refractory anemia (RA) or RA with ringed sideroblasts (RARS) vs RA with excess blasts (RAEB) vs RAEB in transformation (RAEB-t) vs juvenile myelomonocytic leukemia (JMML)).

Patients undergo complete medical and physical examination. Patients are screened for the following aberrations: -7, +8, +21, t(8;21), t(15;17), and inv(16). Smears of peripheral blood and bone marrow, as well as bone marrow biopsies and all cytogenetic and molecular studies performed on blood or bone marrow, are evaluated by a panel of international experts.

Patients with progressive RA or RARS undergo allogeneic stem cell transplantation (ASCT) according to EWOG-MDS SCT studies. Patients with stable RA or RARS wait for an optimal donor before undergoing ASCT. Patients with RAEB with fewer than 15% bone marrow blasts undergo ASCT. Patients with RAEB with at least 15% bone marrow blasts and patients with RAEB-t with fewer than 30% bone marrow blasts receive standard acute myeloid leukemia (AML) induction therapy and then undergo ASCT. Patients with RAEB-t with at least 30% bone marrow blasts are considered for standard AML induction therapy.

Patients with advanced JMML undergo evaluation for splenectomy and receive chemotherapy with mercaptopurine and cytarabine every 3-4 weeks (for 1-4 doses). Patients then undergo ASCT.

Patients are followed every 6 months.

PROJECTED ACCRUAL: Not specified
Study Started
Jul 31
1998
Last Update
Sep 17
2013
Estimate

Drug cytarabine

Drug mercaptopurine

Other laboratory biomarker analysis

Procedure allogeneic bone marrow transplantation

Procedure biopsy

Procedure peripheral blood stem cell transplantation

Criteria 

DISEASE CHARACTERISTICS:

Morphologically confirmed primary myelodysplastic syndromes (MDS)

Diagnosed between July 1, 1998 and June 30, 2002
No prior aplastic anemia

No prior congenital bone marrow failure syndrome, such as:

Fanconi's anemia
Kostmann syndrome
Shwachman syndrome
Dyskeratosis congenital
Amegakaryocytic thrombocytopenia
Diamond-Blackfan anemia
No Down syndrome

None of the following cytogenetic or molecular abnormalities:

t(8;21)(q22;q22)
t(15;17)(q22;q12)
inv(16)(p13;q22)
No typical clinical and cytogenetic features of acute myeloid leukemia FAB M7 (i.e., acute megakaryocytic leukemia) with fewer than 30% blasts in bone marrow or peripheral blood

PATIENT CHARACTERISTICS:

Age

Under 19

Performance status

Not specified

Life expectancy

Not specified

Hematopoietic

See Disease Characteristics

Hepatic

Not specified

Renal

Not specified

Other

No other concurrent illness that would preclude study

PRIOR CONCURRENT THERAPY:

Biologic therapy

Not specified

Chemotherapy

No prior chemotherapy for MDS

Endocrine therapy

Not specified

Radiotherapy

No prior radiotherapy for MDS

Surgery

Not specified
No Results Posted