Yeo, Winnie, Ngai, Nicole T.Y., Yip, CHristopher C.H., Mo, Frankie K.F., Yeo, Victoria A., Ko, Jonathan W.H., Li, Leung V., Lau, Thomas K.H., Lai, Kwai Tung, Pang, Elizabeth, Yip, Claudia H.W., Yeo, Horatio L., Kwok, Carol Chi Hei, Ko, Stephanie W.Y. and Molassiotis, Alex (2024). Risk Factors Associated with Chemotherapy-Induced Nausea and Vomiting Among Women with Breast Cancer Receiving Highly Emetogenic Chemotherapy:Individual Patient-Based Analysis of Three Prospective Antiemetic Trials. Cancer Management and Research, 16 , pp. 283-297.
Abstract
Purpose: Although risk factors related to chemotherapy-induced nausea and vomiting (CINV) have been identified in previous studies, only a few studies have evaluated the risk factors associated with contemporary antiemetic prophylaxis, including olanzapine/ aprepitant-or NEPA-containing regimens. This study aimed to identify the risk factors associated with CINV development in Chinese breast cancer patients receiving doxorubicin and cyclophosphamide chemotherapy. Methods: Data from 304 patients enrolled in 3 previously reported prospective antiemetic studies were included. Multivariate logistic regression models were used to predict risk factors associated with CINV occurrence. Additionally, the likelihood of treatment failure in relation to the number of risk factors in individual patients was evaluated. Results: Multivariate analysis of the entire study group revealed that obesity status (defined as body mass index/= 25.0 kg/m2) and the use of olanzapine/aprepitant-or NEPA-containing anti-emetic regimens were associated with a high likelihood, while a history of motion sickness was associated with a lower likelihood, complete response (CR), and “no nausea” in the overall phase. A history of vomiting during pregnancy was also associated with a lower likelihood of an overall CR. Patients with an increasing number of risk factors had a higher likelihood of treatment failure and shorter time to first vomiting. Those who did not achieve CR and “no nausea” in the first cycle were less likely to achieve these parameters in the subsequent cycle of chemotherapy. Conclusion: The present study confirmed previously reported risk factors for CINV in Chinese breast cancer patients receiving doxorubicin and cyclophosphamide. Further optimization of CINV control is required for patients with identifiable risk factors; olanzapine/aprepitant-or NEPA-containing prophylaxis are the preferred contemporary anti-emetics regimens for Chinese breast cancer patients undergoing doxorubicin and cyclophosphamide chemotherapy.
| Publication DOI: | https://doi.org/10.2147/CMAR.S447546 |
|---|---|
| Divisions: | College of Health & Life Sciences > School of Psychology College of Health & Life Sciences Aston University (General) |
| Funding Information: | This study was supported by an education grant from Madam Diana Hon Fun Kong Donation for Cancer Research. |
| Additional Information: | (c) 2024 Yeo et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.phpand incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the workyou hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Forpermission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
| Uncontrolled Keywords: | aprepitant,cytotoxic,nausea and vomiting,NEPA,olanzapine,Oncology |
| Publication ISSN: | 1179-1322 |
| Data Access Statement: | All data relevant to the study are included in the article or uploaded as supplementary information. The data are availablefrom the Comprehensive Cancer Trials Unit of the Department of Clinical Oncology, Chinese University of Hong Kong,but restrictions apply to the availability of these data. These data were used under permission for the current study, and soare not publicly available. Data are, however, available from the authors (W Yeo and F Mo) upon reasonable request.Data will be made available for 15 years from the start of the clinical trials. |
| Last Modified: | 16 Feb 2026 08:14 |
| Date Deposited: | 11 Feb 2026 15:17 |
| Full Text Link: | |
| Related URLs: |
http://www.scop ... tnerID=8YFLogxK
(Scopus URL) https://www.dov ... xt-article-CMAR (Publisher URL) |
PURE Output Type: | Article |
| Published Date: | 2024-04-08 |
| Accepted Date: | 2024-03-22 |
| Authors: |
Yeo, Winnie
Ngai, Nicole T.Y. Yip, CHristopher C.H. Mo, Frankie K.F. Yeo, Victoria A. Ko, Jonathan W.H. Li, Leung V. Lau, Thomas K.H. Lai, Kwai Tung Pang, Elizabeth Yip, Claudia H.W. Yeo, Horatio L. Kwok, Carol Chi Hei Ko, Stephanie W.Y. Molassiotis, Alex (
0000-0001-6351-9991)
|
0000-0001-6351-9991