Hycanthone Dose-Response in Treatment of Schistosomiasis Mansoni in St. Lucia

J. A. Cook Research and Control Department, Ministry of Health, London School of Hygiene and Tropical Medicine, P. O. Box 93, Castries, St. Lucia, West Indies, England

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P. Jordan Research and Control Department, Ministry of Health, London School of Hygiene and Tropical Medicine, P. O. Box 93, Castries, St. Lucia, West Indies, England

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P. Armitage Research and Control Department, Ministry of Health, London School of Hygiene and Tropical Medicine, P. O. Box 93, Castries, St. Lucia, West Indies, England

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Clinical trials of hycanthone (single intramuscular dose) were undertaken in schistosomiasis mansoni patients in St. Lucia at five dose levels: 3.0, 2.5, 2.0, 1.5, and 1.0 mg/kg body weight. The most common side effect, vomiting, decreased in frequency from 51% at the highest dose to 3% at the lowest; minor side effects showed a similar trend. Three fecal specimens were examined before and at 6 months after treatment by qualitative, quantitative, and hatching techniques. All dose levels caused reductions in egg excretion of 89 to 98%. Rates of cure (absence of eggs by all three methods) according to dose (descending), pretreatment egg output (0–19, 20–49, 50–399, 400+ eggs/ml feces), and age (0–7, 8–14, 15–29, 30+ years) were analyzed to estimate the effect of each variable if the others had been constant. For dose, the standardized percentage success rates were 53.9%, 62.0%, 51.2%, 54.0%, and 27.4%; for egg output, 67.0%, 51.8%, 43.2%, and 21.7%; and for age, 25.2%, 34.5%, 59.3%, and 57.4%. Logit regression analysis shows a significant difference in cure rate (a) between the lowest dose and all others, among which latter there was no difference, (b) between patients excreting 0 to 49 eggs/ml before treatment and those excreting 50+ eggs/ml, and (c) between the age groups 0 to 14 and 15+ years. All dose levels caused some regression in enlargement of liver or spleen. A dose of 1.5 to 2.0 mg/kg body weight is considered to be as effective as one of 3.0 mg/kg and more acceptable for a control program because of the marked reduction in side effects.

Author Notes

Staff member, The Rockefeller Foundation.

External staff, British Medical Research Council; seconded to The Rockefeller Foundation.

Professor of Medical Statistics, London School of Hygiene and Tropical Medicine.

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