TY - JOUR
T1 - Chemotherapy-induced nausea and vomiting is less controlled at delayed phase in patients with esophageal cancer
T2 - A prospective registration study by the CINV Study Group of Japan
AU - Baba, Yoshifumi
AU - Baba, Hideo
AU - Yamamoto, Sachiko
AU - Shimada, Hideaki
AU - Shibata, Tomotaka
AU - Miyazaki, Tatsuya
AU - Yoshikawa, Takaki
AU - Nakajima, Yasuaki
AU - Tsuji, Yasushi
AU - Shimokawa, Mototsugu
AU - Kitagawa, Yuko
AU - Aiba, Keisuke
N1 - Publisher Copyright:
© 2016 International Society for Diseases of the Esophagus.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Chemotherapy is an indispensable therapeutic approach for esophageal cancer. Although chemotherapy-induced nausea and vomiting (CINV) is one of the most crucial adverse events, the current state of CINV in patients with esophageal cancer remains unclear. This multicenter prospective observational study analyzed data for 192 patents with esophageal cancer who underwent moderately emetogenic chemotherapy (MEC) or highly emetogenic chemotherapy (HEC). The patients recorded their CINV incidence and severity daily for 7 days after receiving chemotherapy, using visual analog scales (VAS). Of the 192 patients, 181 receivedHEC including cisplatin, and 11 patients receivedMEC including nedaplatin. Approximately 81% of HEC and 82% of MEC patients received antiemetic therapy in compliance with guidelines. Although CINV was controlled relatively well in the early phase (days 1-4), it was not fully controlled in late phase (days 5-7) for both the HEC and MEC groups. Female sex was a major risk factor for delayed vomiting (P=0.034). Multivariate logistic regression analysis for VAS revealed that motion sickness, age, and use of other antiemetics were risk factors for delayed nausea. Adherence to antiemetic guidelines effectively controls vomiting but is less effective against delayed CINV in both HEC and MEC patients. Identification of individual risk factors, such as female sex, will help develop personalized treatments for CINV. In the clinical setting for esophageal cancer, regimens that include nedaplatin might need to be treated as HEC.
AB - Chemotherapy is an indispensable therapeutic approach for esophageal cancer. Although chemotherapy-induced nausea and vomiting (CINV) is one of the most crucial adverse events, the current state of CINV in patients with esophageal cancer remains unclear. This multicenter prospective observational study analyzed data for 192 patents with esophageal cancer who underwent moderately emetogenic chemotherapy (MEC) or highly emetogenic chemotherapy (HEC). The patients recorded their CINV incidence and severity daily for 7 days after receiving chemotherapy, using visual analog scales (VAS). Of the 192 patients, 181 receivedHEC including cisplatin, and 11 patients receivedMEC including nedaplatin. Approximately 81% of HEC and 82% of MEC patients received antiemetic therapy in compliance with guidelines. Although CINV was controlled relatively well in the early phase (days 1-4), it was not fully controlled in late phase (days 5-7) for both the HEC and MEC groups. Female sex was a major risk factor for delayed vomiting (P=0.034). Multivariate logistic regression analysis for VAS revealed that motion sickness, age, and use of other antiemetics were risk factors for delayed nausea. Adherence to antiemetic guidelines effectively controls vomiting but is less effective against delayed CINV in both HEC and MEC patients. Identification of individual risk factors, such as female sex, will help develop personalized treatments for CINV. In the clinical setting for esophageal cancer, regimens that include nedaplatin might need to be treated as HEC.
KW - Antiemetic guidelines
KW - Antiemetics
KW - CINV
KW - Chemotherapy
KW - Esophageal cancer
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U2 - 10.1111/dote.12482
DO - 10.1111/dote.12482
M3 - Article
C2 - 27001532
AN - SCOPUS:84962579401
SN - 1120-8694
VL - 30
JO - Diseases of the Esophagus
JF - Diseases of the Esophagus
IS - 2
M1 - 12482
ER -