TY - JOUR
T1 - A prospective observational study on chemotherapy-induced nausea and vomiting (CINV) in patients with gynecologic cancer by the CINV Study Group of Japan
AU - Mizuno, Mika
AU - Hiura, Masamichi
AU - Kikkawa, Fumitaka
AU - Numa, Fumitaka
AU - Yaegashi, Nobuo
AU - Narahara, Hisashi
AU - Aoki, Daisuke
AU - Kimura, Eizo
AU - Kato, Hisamori
AU - Shimokawa, Mototsugu
AU - Sugiyama, Toru
AU - Kamura, Toshiharu
N1 - Funding Information:
Mika Mizuno received lecture fees from Chugai Pharmaceutical Co. Ltd. Daisuke Aoki received honoraria or research grants from Ono Pharmaceutical Co., Glaxo Smith Kine K.K., Taiho Pharmaceutical Co., and Chugai Pharmaceutical Co. Ltd. The other authors have no conflict of interest. This study was supported by a research grant from the Public Health Research Foundation, Tokyo, Japan.
Publisher Copyright:
© 2016 Elsevier Inc. All rights reserved.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Objective This study was performed to investigate the occurrence of and risk factors for chemotherapy-induced nausea and vomiting (CINV) in patients with gynecologic cancer. Methods In total, 214 patients with gynecologic cancer who underwent highly emetogenic (HEC) or moderately emetogenic chemotherapy (MEC) were evaluated. We investigated the relationship between CINV and clinical factors and the accuracy of estimation of CINV by medical staff in the acute and late phases. Vomiting was evaluated in terms of frequency, and nausea was evaluated with a 100-mm visual analog scale on days 1 to 7. We also analyzed the risk factors and changes in CINV over time using a generalized linear mixed (GLM) model. Results The multivariate analysis revealed no significant risk factors for acute CINV. The independent risk factors for delayed nausea were a morning sickness history (odds ratio [OR], 2.687; 95% confidence interval [95% CI], 1.450-4.976; p = 0.0017), age (each 1-year increment) (OR, 0.97; 95% CI, 0.944-0.996; p = 0.0235), and HEC (OR, 2.134; 95% CI, 1.039-4.383; p = 0.0391). The GLM model demonstrated that the independent factors affecting nausea were significant morning sickness (p = 0.0101) and HEC (p = 0.0136). These data also showed more severe nausea from days 3 to 5, but the negative predictive value for estimation of delayed nausea by medical staff was 57.8%. Conclusion Our data suggest that improvement of preventive antiemetic administration is needed for patients with risk factors to manage delayed CINV caused by HEC and by MEC.
AB - Objective This study was performed to investigate the occurrence of and risk factors for chemotherapy-induced nausea and vomiting (CINV) in patients with gynecologic cancer. Methods In total, 214 patients with gynecologic cancer who underwent highly emetogenic (HEC) or moderately emetogenic chemotherapy (MEC) were evaluated. We investigated the relationship between CINV and clinical factors and the accuracy of estimation of CINV by medical staff in the acute and late phases. Vomiting was evaluated in terms of frequency, and nausea was evaluated with a 100-mm visual analog scale on days 1 to 7. We also analyzed the risk factors and changes in CINV over time using a generalized linear mixed (GLM) model. Results The multivariate analysis revealed no significant risk factors for acute CINV. The independent risk factors for delayed nausea were a morning sickness history (odds ratio [OR], 2.687; 95% confidence interval [95% CI], 1.450-4.976; p = 0.0017), age (each 1-year increment) (OR, 0.97; 95% CI, 0.944-0.996; p = 0.0235), and HEC (OR, 2.134; 95% CI, 1.039-4.383; p = 0.0391). The GLM model demonstrated that the independent factors affecting nausea were significant morning sickness (p = 0.0101) and HEC (p = 0.0136). These data also showed more severe nausea from days 3 to 5, but the negative predictive value for estimation of delayed nausea by medical staff was 57.8%. Conclusion Our data suggest that improvement of preventive antiemetic administration is needed for patients with risk factors to manage delayed CINV caused by HEC and by MEC.
KW - Antiemetics
KW - Chemotherapy
KW - Gynecologic cancer
KW - Nausea
KW - Vomiting
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U2 - 10.1016/j.ygyno.2015.12.029
DO - 10.1016/j.ygyno.2015.12.029
M3 - Article
C2 - 26748216
AN - SCOPUS:84959487074
SN - 0090-8258
VL - 140
SP - 559
EP - 564
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -