TY - JOUR
T1 - Effects of palonosetron on nausea and vomiting induced by multiple-day chemotherapy
T2 - A retrospective study
AU - Hamano, Hirofumi
AU - Mitsuhashi, Chisato
AU - Suzuki, Yoshiko
AU - Zamami, Yoshito
AU - Tsujinaka, Kaito
AU - Okada, Naoto
AU - Niimura, Takahiro
AU - Hayama, Tatsuya
AU - Imai, Toru
AU - Ishida, Shunsuke
AU - Sakamoto, Kumiko
AU - Goda, Mitsuhiro
AU - Takechi, Kenshi
AU - Yagi, Kenta
AU - Chuma, Masayuki
AU - Horinouchi, Yuya
AU - Shinomiya, Kazuaki
AU - Ikeda, Yasumasa
AU - Kirino, Yasushi
AU - Nakamura, Toshimi
AU - Yanagawa, Hiroaki
AU - Hamada, Yasuhiro
AU - Ishizawa, Keisuke
N1 - Publisher Copyright:
© 2021 Pharmaceutical Society of Japan. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Patients who undergo multiple-day chemotherapy sessions experience hard-to-treat nausea and vomiting. Currently, there is no effective standard treatment for this condition. This study compared the preventive effect of first-generation 5-hydroxytryptamine 3 receptor antagonists (5-HT3 RAs) and second-generation 5-HT3 RAs palonosetron in multiple-day chemotherapy-induced nausea and vomiting. The design of this study was a retrospective case-control study of patients who received a five-day cisplatin-based chemotherapy and were treated with aprepitant, dexamethasone, granisetron, and ramosetron or palonosetron. The patients were divided into two groups: patients given granisetron and ramosetron (the first-generation group), and those given palonosetron (palonosetron group). The percentage of patients with a complete response or total control was assessed. They were divided into three phases: 0–216h (overall phase), 0–120h (remedial phase), and 120–216h (after phase). The remedial phase was further divided into 0–24h (early phase) and 24–120h (later phase). Moreover, the nutritional status of each patient was assessed by noting the patients’ total calorie-intake per day and total parenteral nutrition. First-generation 5-HT3 RAs and palonosetron were used for treatment in 18 and 28 patients, respectively. The complete response rate and caloric oral intake of the later phase were higher in the palonosetron group than in the first-generation group. We conclude that palonosetron treatment was more effective than first-generation 5-HT3 RAs in controlling multiple-day chemotherapy-induced nausea and vomiting.
AB - Patients who undergo multiple-day chemotherapy sessions experience hard-to-treat nausea and vomiting. Currently, there is no effective standard treatment for this condition. This study compared the preventive effect of first-generation 5-hydroxytryptamine 3 receptor antagonists (5-HT3 RAs) and second-generation 5-HT3 RAs palonosetron in multiple-day chemotherapy-induced nausea and vomiting. The design of this study was a retrospective case-control study of patients who received a five-day cisplatin-based chemotherapy and were treated with aprepitant, dexamethasone, granisetron, and ramosetron or palonosetron. The patients were divided into two groups: patients given granisetron and ramosetron (the first-generation group), and those given palonosetron (palonosetron group). The percentage of patients with a complete response or total control was assessed. They were divided into three phases: 0–216h (overall phase), 0–120h (remedial phase), and 120–216h (after phase). The remedial phase was further divided into 0–24h (early phase) and 24–120h (later phase). Moreover, the nutritional status of each patient was assessed by noting the patients’ total calorie-intake per day and total parenteral nutrition. First-generation 5-HT3 RAs and palonosetron were used for treatment in 18 and 28 patients, respectively. The complete response rate and caloric oral intake of the later phase were higher in the palonosetron group than in the first-generation group. We conclude that palonosetron treatment was more effective than first-generation 5-HT3 RAs in controlling multiple-day chemotherapy-induced nausea and vomiting.
KW - 5-hydroxytryptamine 3 antagonist
KW - Chemotherapy-induced nausea and vomiting
KW - Multiple-day chemotherapy
KW - Palonosetron
KW - Supportive care
UR - http://www.scopus.com/inward/record.url?scp=85103744443&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85103744443&partnerID=8YFLogxK
U2 - 10.1248/BPB.B20-00609
DO - 10.1248/BPB.B20-00609
M3 - Article
C2 - 33790099
AN - SCOPUS:85103744443
SN - 0918-6158
VL - 44
SP - 478
EP - 484
JO - Biological and Pharmaceutical Bulletin
JF - Biological and Pharmaceutical Bulletin
IS - 4
ER -