Abstract

The anti-emetic efficacy and safety of granisetron, a highly selective and potent 5-HT3 receptor antagonist, was compared with that of high-dose metoclopramide plus dexamethasone in 281 patients due to receive single-day cisplatin chemotherapy (> or = 49 mg m-2). In this single-blind, multicentre study, granisetron (40 micrograms kg-1) was administered as a single prophylactic 5-min infusion. Dexamethasone (12 mg) was administered as a 30-min infusion followed by a loading dose of 3 mg kg-1 metoclopramide. A maintenance dose of metoclopramide 4 mg kg-1 was then infused over 8 h. A single prophylactic dose of granisetron was as effective as the combination regimen in the prevention of cisplatin-induced emesis. Of 143 granisetron-treated patients, 100 (70%) were complete responders (no vomiting and no or only mild nausea) compared with 93/138 (67%) patients who received the comparator regimen. Twenty-three percent of granisetron-treated patients experienced one of more adverse events compared with 33% of patients in the comparator group. No extrapyramidal reactions were reported in the granisetron group compared with 13 in comparator-treated patients (8%). This difference was significant (P < 0.05). The commonest adverse event in the granisetron group, headache (9.8%) described by the majority of patients as mild, was significantly higher than that reported in the comparator group (3% P = 0.02). Granisetron appears to be a safe and effective agent which can be used as a single agent for the prophylaxis of cisplatin-induced emesis. The simplicity of administration, a single 5-min infusion prior to chemotherapy, and the lack of somnolence or extrapyramidal reactions offer clear advantages over the comparator combination regimen.

Highlights

  • The chemotherapy was to be administered on a single day and cisplatin was to be administered at a minimum dose of > 49 mg m2

  • Two hundred and eighty-one patients participated in the study (183 males and 98 females)

  • One hundred and forty-three patients received anti-emetic treatment with granisetron and 138 with the comparator regimen of metoclopramide combined with dexamethasone

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Summary

Methods

PatientsThe study was conducted at 28 centres in four countries (France, Switzerland, UK and West Germany). Patients eligible for selection into this study were inpatients due to receive cisplatin-containing chemotherapy for the first time for the treatment of malignant disease. The chemotherapy was to be administered on a single day and cisplatin was to be administered at a minimum dose of > 49 mg m2. Patients were excluded from the study if they had marked hepatic or renal dysfunction, active gastric ulceration, gastric compression or were suffering from acute or chronic nausea or vomiting. All patients gave their informed consent to participate in the study and were free to withdraw at any time.

Results
Discussion
Conclusion

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