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  • 1
    ISSN: 1437-7772
    Keywords: granisetron ; prevention ; nausea ; vomiting ; cancer chemotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background We investigated the efficacy and safety of granisetron in 40 pediatric oncology patients who received identical chemotherapy regimens for three courses. Methods During the first course, the emetogenicity of each chemotherapy regimen was evaluated without granisetron. Next patients received one of two doses of intravenous granisetron, i.e. 20 or 40 mcg/kg during the second and third course of chemotherapy in a cross-over fashion. Results Out of the 40 patients, two children had no emetic episode during the 24 hour period following commencement of the first course of chemotherapy. Whereas, 23 patients receiving 20 μ/kg granisetron, and 22 patients receiving 40 μ/kg, obtained complete response (no emetic episode during the 24 hour period following commencement of chemotherapy) in the second or third course. When patients received 20 or 40 μ/kg of granisetron, all measured efficacy parameters were superior in comparison to the period when they were receiving no granisetron. There was no significant difference in the antiemetic effect between the two doses of granisetron. However, a dose-related improvement in efficacy was observed with granisetron in a certain subset of patients; that is, 4 of the 10 patients receiving 20 μ/kg, who had responded poorly with respect to nausea and vomiting, showed a complete or major response when the dose was increased to 40 μ/kg. One child developed somnolence. No other adverse events were observed. Conclusion Granisetron is an effective and safe antiemetic for children receiving intensive chemotherapy regimens containing cisplatin, cyclophosphamide or methotrexate. When comparing the two doses of 20 and 40 μ/kg, 40 μ/kg appeared more effective; although the difference was not statistically significant.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Normal marrow cell kinetics were studied by flow cytometry with computer analysis in 11 children with malignancies who received high-dose MTX followed by CF rescue. Nine children with hematological tumors in remission each received an infusion of MTX over 24 h, followed by delayed CF rescue. In 8 of the 9, an accumulation of cells in early to mid-S phase and a decrease of cells in G2/M phase were observed at 24–48 h after the beginning of the MTX infusion. At 144 h after MTX infusion this kinetic perturbation disappeared and the DNA histogram returned to the same state as before therapy. Two children who had malignant bone tumors without marrow infiltration each received an infusion of MTX over 6 h with early CF rescue following an initial IV injection of vincristine. They did not have any prominent perturbation of marrow cell kinetics after MTX exposure, except for a transient increase of cells in G2/M phase. These results confirm that with the high-dose MTX therapy described above for hematological malignancies the impairment of marrow cell kinetics was much more severe and was soon followed by complete recovery, whereas with the therapy for solid tumors the impairment was much slighter.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cancer chemotherapy and pharmacology 13 (1984), S. 9-13 
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The renal excretion of methotrexate (MTX) and its major metabolite 7-hydroxymethotrexate (7-OH-MTX) was analysed in 12 children with malignancies during 52 courses of high-dose methotrexate (H-D-MTX) infusion at dosages ranging from 0.7 to 8.4 g/m2. The peak concentrations of both MTX and 7-OH-MTX exceeded the aqueous solubilities of these compounds at low pH (≦6.0). The cumulative MTX excretion in urine was 75%–98% of the administered amount of MTX, and the cumulative 7-OH-MTX excretion in the urine was 3%–15%. The theoretically required urinary flow (TRUF) was estimated as the minimum urine volume needed for complete resolution of MTX and its metabolites in urine. TRUF during MTX infusion from 0 to 6 h and from 6 to 12 h was correlated with the dosage of MTX, and these values were 0.1–1.8 ml/min/m2 at pH 7.0, 0.5–11.1 ml/min/m2 at pH 6.0, and 1.9–42.2 ml/min/m2 at pH 5.0 with dosages of 0.7 to 8.4 g/m2. The value of the theoretically required urinary flow is important to ensure adequate hydration and the optimum alkalinization schedule for massive MTX infusion.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1971
    Keywords: Myocardial fibrosis ; Myocarditis ; QS pattern
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A QS pattern in the right precordial leads of the electrocardiogram was noted in a 9-year-old asymptomatic boy. Echocardiography revealed paradoxical movement of the interventricular septum, which showed interstitial myocardial fibrosis in the biopsy specimen and a defective uptake of thallium-201. Extensive myocardial fibrosis was probably a sequela of an attack of myocarditis in infancy.
    Type of Medium: Electronic Resource
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