1226 Ondansetron vs granisetron, both combined with dexamethasone in the prevention of cisplatin-induced emesis

From December 1992 to July 1994, 973 consecutive patients scheduled to receive for the first time cisplatin at doses ≥ 50 mg/m 2, used alone or in combination with other antineoplastic agents, entered a doubleblind multicenter randomized study comparing ondansetron (OND) 8 mg iv vs granisetron (GRAN...

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Published inEuropean journal of cancer (1990) Vol. 31; p. S256
Main Authors Roila, F., De Angelis, V., Moretti, G., Tateo, S., Cascinu, S., Ionta, M.T., Montinari, F., Morritti, M., Pusceddu, G., Favalli, G., Cortesi, E., Dazzi, C., Ballatori, E.
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.11.1995
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Abstract From December 1992 to July 1994, 973 consecutive patients scheduled to receive for the first time cisplatin at doses ≥ 50 mg/m 2, used alone or in combination with other antineoplastic agents, entered a doubleblind multicenter randomized study comparing ondansetron (OND) 8 mg iv vs granisetron (GRAN) 3 mg iv, both diluted in 50 ml normal saline and administered in 15 minutes, 30 minutes before chemotherapy. Dexamethasone (DEX) 20 mg iv was added to the 5-HT 3 antagonists and administered in 15 min, 45 min befure chemotherapy. Nine hundred and sixty-six patients (483 receiving OND and 483 GRAN) were evaluable for intention to treat analysis. Patient characteristics were well balanced between the two antiemetic treatments. Complete protection from acute vomiting/nausea was obtained in 383 (79.3%)/348 (72.1%) of patients receiving OND and in 386 (79.9%)/347 (71.8%) of those receiving GRAN. During day 2–4 after chemotherapy patients received the same antiemetic prophylaxis for delayed emesis (metoclopramide 20 mg 4 times/day + DEX 8 mg im × 2 on day 2–3 and 4 mg im × 2 on day 4). Complete protection on day 2–6 from vomiting/nausea was obtained in 69.7%/52.9% and 70.0%/49.6%, respectively. Adverse events were mild and not significantly different between the two antiemetic regimens. In conclusion, OND 8 mg and GRAN 3 mg, both combined with DEX, showed similar efficacy and tolerability in the prevention of acute and delayed cisplatin-induced emesis; therefure, the choice between them should be made on the basis of acquisition costs. Supported by AUCC (Associazione Umbra Contro il Cancro).
AbstractList From December 1992 to July 1994, 973 consecutive patients scheduled to receive for the first time cisplatin at doses ≥ 50 mg/m 2, used alone or in combination with other antineoplastic agents, entered a doubleblind multicenter randomized study comparing ondansetron (OND) 8 mg iv vs granisetron (GRAN) 3 mg iv, both diluted in 50 ml normal saline and administered in 15 minutes, 30 minutes before chemotherapy. Dexamethasone (DEX) 20 mg iv was added to the 5-HT 3 antagonists and administered in 15 min, 45 min befure chemotherapy. Nine hundred and sixty-six patients (483 receiving OND and 483 GRAN) were evaluable for intention to treat analysis. Patient characteristics were well balanced between the two antiemetic treatments. Complete protection from acute vomiting/nausea was obtained in 383 (79.3%)/348 (72.1%) of patients receiving OND and in 386 (79.9%)/347 (71.8%) of those receiving GRAN. During day 2–4 after chemotherapy patients received the same antiemetic prophylaxis for delayed emesis (metoclopramide 20 mg 4 times/day + DEX 8 mg im × 2 on day 2–3 and 4 mg im × 2 on day 4). Complete protection on day 2–6 from vomiting/nausea was obtained in 69.7%/52.9% and 70.0%/49.6%, respectively. Adverse events were mild and not significantly different between the two antiemetic regimens. In conclusion, OND 8 mg and GRAN 3 mg, both combined with DEX, showed similar efficacy and tolerability in the prevention of acute and delayed cisplatin-induced emesis; therefure, the choice between them should be made on the basis of acquisition costs. Supported by AUCC (Associazione Umbra Contro il Cancro).
Author Tateo, S.
Montinari, F.
Dazzi, C.
Cortesi, E.
Ballatori, E.
Pusceddu, G.
Roila, F.
Ionta, M.T.
Morritti, M.
Cascinu, S.
Moretti, G.
Favalli, G.
De Angelis, V.
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