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pubmed-article:2793376pubmed:abstractTextSpirogermanium was given as a 90 minute infusion to 47 eligible patients with refractory Hodgkin's (9 patients) or non-Hodgkin's lymphoma (38 patients). The schedule was 80 mg/m2 three times a week for the first two weeks and 100 mg/m2, 3 times a week, for the two subsequent weeks. In case of response or stable disease, the treatment was continued with biweekly infusions of 100 mg/m2 until tumor progression. In 64% of cases, three or more combinations had been previously administered; 66% of patients presented an extra-lymphatic spread of disease. Two patients with Hodgkin's disease showed a partial response of 11 and 23 weeks and two patients with non-Hodgkin's lymphoma achieved a complete response of 12 and 24 weeks. Overall, 14 patients showed a tumor progression within the first month of treatment. The main toxicity was neurological, with dizziness and lethargy during the infusion in 50% of cases. Hematologic toxicity was almost absent. Spirogermanium is ineffective in heavily pretreated patients with non-Hodgkin's lymphoma. The confirmed lack of activity in patients with refractory malignant lymphoma and the need of repeated and prolonged infusions definitely discourage the clinical use of the drug.lld:pubmed
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pubmed-article:2793376pubmed:pagination219-22lld:pubmed
pubmed-article:2793376pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:2793376pubmed:year1989lld:pubmed
pubmed-article:2793376pubmed:articleTitleA phase II study of spirogermanium in patients with advanced malignant lymphoma.lld:pubmed
pubmed-article:2793376pubmed:affiliationServizio Oncologico, Ospedale San Giovanni, Bellinzona, Switzerland.lld:pubmed
pubmed-article:2793376pubmed:publicationTypeJournal Articlelld:pubmed