Aprepitant plus granisetron and dexamethasone for prevention of chemotherapy-induced nausea and vomiting in patients with gastric cancer treated with S-1 plus cisplatin

Background We aimed to evaluate the efficacy of a new combination antiemetic therapy comprising aprepitant, granisetron, and dexamethasone in gastric cancer patients undergoing chemotherapy with cisplatin and S-1. Methods Gastric cancer patients scheduled to receive their first course of chemotherap...

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Published in:Journal of gastroenterology Vol. 48; no. 11; pp. 1234 - 1241
Main Authors: Oyama, Katsunobu, Fushida, Sachio, Kaji, Masahide, Takeda, Toshiya, Kinami, Shinichi, Hirono, Yasuo, Yoshimoto, Katsuhiro, Yabushita, Kazuhisa, Hirosawa, Hisashi, Takai, Yuki, Nakano, Tatsuo, Kimura, Hironobu, Yasui, Toshiaki, Tsuneda, Atsushi, Tsukada, Tomoya, Kinoshita, Jun, Fujimura, Takashi, Ohta, Tetsuo
Format: Journal Article
Language:English
Published: Tokyo Springer Japan 01-11-2013
Springer
Springer Nature B.V
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Summary:Background We aimed to evaluate the efficacy of a new combination antiemetic therapy comprising aprepitant, granisetron, and dexamethasone in gastric cancer patients undergoing chemotherapy with cisplatin and S-1. Methods Gastric cancer patients scheduled to receive their first course of chemotherapy with cisplatin (60 mg/m 2 ) and S-1 (80 mg/m 2 ) were treated with a new combination antiemetic therapy aprepitant, granisetron, and dexamethasone on day 1; aprepitant and dexamethasone on days 2 and 3; and dexamethasone on day 4. The patients reported vomiting, nausea, use of rescue therapy, and change in the amount of diet intake, and completed the Functional Living Index-Emesis (FLIE) questionnaire. The primary endpoint was complete response (CR; no emesis and use of no rescue antiemetics) during the overall study phase (0–120 h after cisplatin administration). The secondary endpoints included complete protection (CP; CR plus no significant nausea); change in the amount of diet intake; and the impact of chemotherapy-induced nausea and vomiting (CINV) on daily life during the overall, acute (0–24 h), and delayed (24–120 h) phases. Results Fifty-three patients were included. CR was achieved in 88.7, 98.1, and 88.7 % of patients in the overall, acute, and delayed phases, respectively. The corresponding rates of CP were 67.9, 96.2, and 67.9 %. Approximately half of the patients had some degree of anorexia. FLIE results indicated that 79.5 % of patients reported “minimal or no impact of CINV on daily life”. Conclusions Addition of aprepitant to standard antiemetic therapy was effective in gastric cancer patients undergoing treatment with cisplatin and S-1.
ISSN:0944-1174
1435-5922
DOI:10.1007/s00535-012-0746-1