TY - JOUR
T1 - Preventive effects of low-dose dexamethasone for delayed adverse events induced by carboplatin-based combination chemotherapy
AU - Kawazoe, Hitoshi
AU - Takiguchi, Yoshiharu
AU - Tanaka, Hiroaki
AU - Doi, Chiaki
AU - Fukuoka, Noriyasu
AU - Kanaji, Nobuhiro
AU - Bandoh, Shuji
AU - Ishida, Toshihiko
AU - Houchi, Hitoshi
PY - 2007/6
Y1 - 2007/6
N2 - We performed a retrospective study to examine the protective effect of low-dose dexamethasone (DEX) on delayed adverse events induced by carboplatin (CBDCA)-based combination chemotherapy in patients with thoracic tumors. Low-dose DEX (4-8 mg/day) was administered on day 1 and after, in addition to a serotonin 5-HT3 receptor antagonist. The acute adverse events (day 1) were well controlled in the patients with or without co-treatment of DEX. On the other hand, the delayed nausea, emesis, anorexia, and fatigue after day 2 failed to be controlled by 5-HT3 antagonist alone. Co-treatment with DEX significantly suppressed the grade of the delayed adverse events during days 2-10. The mean ratio of complete protection during days 2-10 were significantly higher in the DEX-treated group compared with the non-DEX-treated group. These results reveal that low-dose DEX is a clinically effective treatment for the prevention of delayed adverse events induced by CBDCA-based combination chemotherapy.
AB - We performed a retrospective study to examine the protective effect of low-dose dexamethasone (DEX) on delayed adverse events induced by carboplatin (CBDCA)-based combination chemotherapy in patients with thoracic tumors. Low-dose DEX (4-8 mg/day) was administered on day 1 and after, in addition to a serotonin 5-HT3 receptor antagonist. The acute adverse events (day 1) were well controlled in the patients with or without co-treatment of DEX. On the other hand, the delayed nausea, emesis, anorexia, and fatigue after day 2 failed to be controlled by 5-HT3 antagonist alone. Co-treatment with DEX significantly suppressed the grade of the delayed adverse events during days 2-10. The mean ratio of complete protection during days 2-10 were significantly higher in the DEX-treated group compared with the non-DEX-treated group. These results reveal that low-dose DEX is a clinically effective treatment for the prevention of delayed adverse events induced by CBDCA-based combination chemotherapy.
KW - Adverse event
KW - Carboplatin
KW - Chemotherapy
KW - Dexamethasone
KW - Nausea
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U2 - 10.1248/yakushi.127.1001
DO - 10.1248/yakushi.127.1001
M3 - Article
C2 - 17541251
AN - SCOPUS:34249775804
SN - 0031-6903
VL - 127
SP - 1001
EP - 1006
JO - Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan
JF - Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan
IS - 6
ER -