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  • Electronic Resource  (2)
  • 1980-1984  (2)
  • Acute lymphocytic leukemia in childhood  (1)
  • Desferrioxamine  (1)
  • 1
    ISSN: 1432-0584
    Keywords: Acute lymphocytic leukemia in childhood ; Intermediate dose methotrexate therapy ; High risk and standard risk differential therapy ; ALL subclassification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary One hundred and eight children with acute lymphocytic leukemia (ALL) were admitted to a prospective therapeutic regime. Remission induction was achieved in 94% of the cases with vincristine, L-asparaginase, adriamycine and prednisone. One hundred and one patients received three intermediate dose methotrexate (MTX) infusions combined with intrathecal MTX, followed by L-asparaginase 24 h later. High risk (HR) patients (n=50) were treated in addition with high dose cyclophosphamide and Ara-C over 3 weeks. One hundred and one patients received cranial irradiation (1,800 rads standard risk (SR)-patients, 2,400 rads HR-patients) and intrathecal MTX. Maintenance therapy was performed with the usual two drug combination of daily 6 mercaptopurine (6 MP) and weekly MTX orally. Based on phenotyping 67% of patients had common type ALL, and pre-T or T-cell type in 18%. Six per cent of the patients had leukemic blasts expressing both common ALL and T-cell markers (c/T-type); 9% had acute undifferentiated leukemia (AUL). Out of 108, 101 achieved a complete remission, 6 patients died during induction therapy, 1 was a non-responder and 9 patients relapsed. Of these 6 had haematological relapses, 2 had CNS relapse and 1 had a testicular relapse. Four patients died in continuous complete remission (CCR). For 101 patients the 30 months probability of CCR is 0.85 (± 0.05). For 51 patients with standard risk CCR probability is 0.98 (± 0.03), for 50 patients with high risk indices it is 0.65 (±0.11). Patients with c-ALL have a CCR survival of 0.85 (±0.07), those with T- or pre-T-ALL 0.88 (±0.09), all 5 patients with c/T-ALL alive in CCR. In our study pediatric AUL patients have the most unfavourable prognosis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 137 (1981), S. 285-290 
    ISSN: 1432-1076
    Keywords: Thalassemia ; Hemosiderosis ; Desferrioxamine ; Liver storage iron ; Ferritin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Ten children with transfusion dependent anemias (thalassemia, sideroblastic anemia, congenital pure red cell aplasia) received either intravenous desferrioxamine (DF) in increasing doses up to 450 mg/kg at the time of transfusion or daily subcutaneous DF up to 110 mg/kg on an outpatient basis. No patient on intravenous DF reached a negative iron balance. All children with a subcutaneous DF dose of more than 60 mg/kg obtained a negative iron balance with a net iron excretion (transfusion iron already substracted) between 206 to 810 mg (mean 496 mg) monthly. The effectiveness of regular subcutaneous DF on liver storage iron could be confirmed in 4 patients by liver biopsy, showing a decrease between 40–60% iron after 12–14 months of chelation therapy. So far the daily iron excretion has remained constant with a given dose of DF over a period up to 15 months. Even if poor compliance in some patients is taken into account, it is possible with this method of treatment to prevent further accumulation of iron in chronically transfused children.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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