TY - JOUR
T1 - Randomized study of dexamethasone treatment for delayed emesis, anorexia and fatigue induced by irinotecan
AU - Inoue, Akira
AU - Yamada, Yasuhide
AU - Matsumura, Yasuhiro
AU - Shimada, Yasuhiro
AU - Muro, Kei
AU - Gotoh, Masahiro
AU - Hamaguchi, Tetsuya
AU - Mizuno, Toshiro
AU - Shirao, Kuniaki
N1 - Funding Information:
Received: 1 January 2003 Accepted: 24 April 2003 Published online: 3 July 2003 © Springer-Verlag 2003 Supported in part by Grants-in-aid for Cancer Research from the Ministry of Health and Welfare and from the Second-term Comprehensive 10-year Strategy for Cancer Control.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - The prevention of post-chemotherapy symptoms such as delayed emesis, anorexia, and fatigue induced by irinotecan has not been studied. We compared the effects of dexamethasone (Dex) with those of a placebo on these symptoms in a randomized study. Seventy patients scheduled to receive irinotecan chemotherapy were enrolled in the study and randomly divided into a treatment of a placebo group. In the treatment group, 8 mg of Dex were administered on days 2-4 after the start of chemotherapy. All patients in both groups received Dex and granisetron for prophylaxis against acute emesis on day 1. We evaluated 68 patients (35 receiving Dex, 33 receiving the placebo). Although delayed emesis was completely prevented in most of patients in both groups (Dex, 82.9%; placebo, 78.8%), anorexia and fatigue were more completely prevented in those in the Dex group (Dex, 62.9% and 77.1%, placebo, 39.4% and 57.6%, respectively). The effect of Dex on improving simultaneous prophylaxis against all three symptoms was almost significant (Dex, 60.0%; placebo, 36.4%; P=0.058). The safety profiles of the two groups were not discernibly different. These results suggest that treatment with Dex may be beneficial to reduce post-chemotherapy symptoms induced by irinotecan, specifically anorexia and fatigue, with acceptable toxicities.
AB - The prevention of post-chemotherapy symptoms such as delayed emesis, anorexia, and fatigue induced by irinotecan has not been studied. We compared the effects of dexamethasone (Dex) with those of a placebo on these symptoms in a randomized study. Seventy patients scheduled to receive irinotecan chemotherapy were enrolled in the study and randomly divided into a treatment of a placebo group. In the treatment group, 8 mg of Dex were administered on days 2-4 after the start of chemotherapy. All patients in both groups received Dex and granisetron for prophylaxis against acute emesis on day 1. We evaluated 68 patients (35 receiving Dex, 33 receiving the placebo). Although delayed emesis was completely prevented in most of patients in both groups (Dex, 82.9%; placebo, 78.8%), anorexia and fatigue were more completely prevented in those in the Dex group (Dex, 62.9% and 77.1%, placebo, 39.4% and 57.6%, respectively). The effect of Dex on improving simultaneous prophylaxis against all three symptoms was almost significant (Dex, 60.0%; placebo, 36.4%; P=0.058). The safety profiles of the two groups were not discernibly different. These results suggest that treatment with Dex may be beneficial to reduce post-chemotherapy symptoms induced by irinotecan, specifically anorexia and fatigue, with acceptable toxicities.
KW - Anorexia
KW - Delayed emesis
KW - Dexamethasone
KW - Fatigue
KW - Irinotecan
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U2 - 10.1007/s00520-003-0488-y
DO - 10.1007/s00520-003-0488-y
M3 - Article
C2 - 12844250
AN - SCOPUS:0043236024
VL - 11
SP - 528
EP - 532
JO - Supportive Care in Cancer
JF - Supportive Care in Cancer
SN - 0941-4355
IS - 8
ER -