Background The combination of a neurokinin-1 receptor antagonist, dexamethasone, and a 5-HT(3) receptor antagonist is currently the standard antiemetic treatment in patients receiving cisplatin-based high emetogenic chemotherapy (HEC). The aim of this study was to evaluate the efficacy of a combination of palonosetron, a unique second-generation 5-HT(3) receptor antagonist, aprepitant, the only approved neurokinin-1 receptor antagonist, and dexamethasone as antiemetic prophylaxis in patients receiving HEC (cisplatin >= 50 mg/mq). Methods Chemotherapy-naive adult patients, receiving cisplatin-based HEC, were treated with palonosetron 0.25 mg/i.v., dexamethasone 20 mg/i.v., and aprepitant 125 mg/p.o., 1-h before chemotherapy. Aprepitant 80 mg/p.o. and dexamethasone 4 mg p.o. were administered on days 2-3. Primary end point was complete response (CR; no vomiting and no use of rescue medication), during the overall study period (0-120 h). Secondary end points were complete control (CR and no more than mild nausea), emesis-free rate, and nausea-free rate during the acute (024 h), delayed (24-120 h), and overall (0-120 h) periods. Safety was also evaluated. Results A total of 222 patients were included in the study. Median age was 62 years, 76.6% were male and 23.4% female, and most common tumors were lung (66.7%) and head and neck (15.8%); 70.3% of patients achieved CR during the overall study period. Complete control, emesis-free rate, and nausea-free rate were 70.3%, 92.8%, and 59.9%, respectively, during the overall phase. The most commonly reported side effects were constipation (39% of patients) and headache (5%). Conclusions This study shows that palonosetron in combination with aprepitant and dexamethasone is effective to prevent chemotherapy-induced nausea and vomiting in patients treated with cisplatin-based HEC.

Palonosetron plus 3-day aprepitant and dexamethasone to prevent nausea and vomiting in patients receiving highly emetogenic chemotherapy / Longo, Flavia; Mansueto, Giovanni; Lapadula, Vittoria; DE SANCTIS, Rita; Quadrini, Silvia; Grande, Roberta; Gori, Bruno; Altavilla, Amelia; D'Antoni, I.; DEL SIGNORE, Ester; Stumbo, Luciano; DE LUCA, Cristina; Cimadon, Barbara; Cortesi, Enrico; Gamucci, Teresa; DI SERI, Marisa. - In: SUPPORTIVE CARE IN CANCER. - ISSN 0941-4355. - 19:8(2011), pp. 1159-1164. [10.1007/s00520-010-0930-x]

Palonosetron plus 3-day aprepitant and dexamethasone to prevent nausea and vomiting in patients receiving highly emetogenic chemotherapy

LAPADULA, VITTORIA;DE SANCTIS, RITA;QUADRINI, SILVIA;GRANDE, Roberta;GORI, BRUNO;ALTAVILLA, AMELIA;DEL SIGNORE, ESTER;STUMBO, Luciano;DE LUCA, CRISTINA;CORTESI, Enrico;DI SERI, Marisa
2011

Abstract

Background The combination of a neurokinin-1 receptor antagonist, dexamethasone, and a 5-HT(3) receptor antagonist is currently the standard antiemetic treatment in patients receiving cisplatin-based high emetogenic chemotherapy (HEC). The aim of this study was to evaluate the efficacy of a combination of palonosetron, a unique second-generation 5-HT(3) receptor antagonist, aprepitant, the only approved neurokinin-1 receptor antagonist, and dexamethasone as antiemetic prophylaxis in patients receiving HEC (cisplatin >= 50 mg/mq). Methods Chemotherapy-naive adult patients, receiving cisplatin-based HEC, were treated with palonosetron 0.25 mg/i.v., dexamethasone 20 mg/i.v., and aprepitant 125 mg/p.o., 1-h before chemotherapy. Aprepitant 80 mg/p.o. and dexamethasone 4 mg p.o. were administered on days 2-3. Primary end point was complete response (CR; no vomiting and no use of rescue medication), during the overall study period (0-120 h). Secondary end points were complete control (CR and no more than mild nausea), emesis-free rate, and nausea-free rate during the acute (024 h), delayed (24-120 h), and overall (0-120 h) periods. Safety was also evaluated. Results A total of 222 patients were included in the study. Median age was 62 years, 76.6% were male and 23.4% female, and most common tumors were lung (66.7%) and head and neck (15.8%); 70.3% of patients achieved CR during the overall study period. Complete control, emesis-free rate, and nausea-free rate were 70.3%, 92.8%, and 59.9%, respectively, during the overall phase. The most commonly reported side effects were constipation (39% of patients) and headache (5%). Conclusions This study shows that palonosetron in combination with aprepitant and dexamethasone is effective to prevent chemotherapy-induced nausea and vomiting in patients treated with cisplatin-based HEC.
2011
Dexamethasone; 5-ht 3 receptor antagonist; cinv; 5-ht(3) receptor antagonist; hec; aprepitant; palonosetron
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Palonosetron plus 3-day aprepitant and dexamethasone to prevent nausea and vomiting in patients receiving highly emetogenic chemotherapy / Longo, Flavia; Mansueto, Giovanni; Lapadula, Vittoria; DE SANCTIS, Rita; Quadrini, Silvia; Grande, Roberta; Gori, Bruno; Altavilla, Amelia; D'Antoni, I.; DEL SIGNORE, Ester; Stumbo, Luciano; DE LUCA, Cristina; Cimadon, Barbara; Cortesi, Enrico; Gamucci, Teresa; DI SERI, Marisa. - In: SUPPORTIVE CARE IN CANCER. - ISSN 0941-4355. - 19:8(2011), pp. 1159-1164. [10.1007/s00520-010-0930-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/872721
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