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Dataset on chemotherapy-induced nausea and vomiting (CINV) and quality of life (QOL) during multiple chemotherapy cycles among a Chinese breast cancer patient population who were randomized to antiemetic regimens with or without olanzapine.关于中国乳腺癌患者群体在多个化疗周期中化疗引起的恶心和呕吐(CINV)及生活质量(QOL)的数据集,这些患者被随机分配至接受或不接受奥氮平的止吐方案。
Data Brief. 2020 Mar 12;30:105421. doi: 10.1016/j.dib.2020.105421. eCollection 2020 Jun.
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本文引用的文献

1
A randomized study of olanzapine-containing versus standard antiemetic regimens for the prevention of chemotherapy-induced nausea and vomiting in Chinese breast cancer patients.一项比较奥氮平与标准止吐方案预防中国乳腺癌患者化疗相关性恶心呕吐的随机研究。
Breast. 2020 Apr;50:30-38. doi: 10.1016/j.breast.2020.01.005. Epub 2020 Jan 14.
2
Olanzapine for the Prevention of Chemotherapy-Induced Nausea and Vomiting.奥氮平用于预防化疗引起的恶心和呕吐。
N Engl J Med. 2016 Jul 14;375(2):134-42. doi: 10.1056/NEJMoa1515725.
3
Efficacy and safety of NEPA, an oral combination of netupitant and palonosetron, for prevention of chemotherapy-induced nausea and vomiting following highly emetogenic chemotherapy: a randomized dose-ranging pivotal study.奈妥吡坦与帕洛诺司琼口服复方制剂NEPA预防高度致吐性化疗后化疗引起的恶心和呕吐的疗效及安全性:一项随机剂量范围关键研究
Ann Oncol. 2014 Jul;25(7):1340-1346. doi: 10.1093/annonc/mdu110. Epub 2014 Mar 7.
4
A randomized study of aprepitant, ondansetron and dexamethasone for chemotherapy-induced nausea and vomiting in Chinese breast cancer patients receiving moderately emetogenic chemotherapy.阿瑞匹坦、昂丹司琼和地塞米松用于接受中度致吐性化疗的中国乳腺癌患者化疗引起的恶心和呕吐的随机研究。
Breast Cancer Res Treat. 2009 Feb;113(3):529-35. doi: 10.1007/s10549-008-9957-9. Epub 2008 Mar 10.

关于中国乳腺癌患者群体在多个化疗周期中化疗引起的恶心和呕吐(CINV)及生活质量(QOL)的数据集,这些患者被随机分配至接受或不接受奥氮平的止吐方案。

Dataset on chemotherapy-induced nausea and vomiting (CINV) and quality of life (QOL) during multiple chemotherapy cycles among a Chinese breast cancer patient population who were randomized to antiemetic regimens with or without olanzapine.

作者信息

Yeo Winnie, Chan Vicky T C, Li Leung, Lau Thomas K H, Lai Kwai Tung, Pang Elizabeth, Cheung Maggie, Mo Frankie K F

机构信息

Department of Clinical Oncology, Prince of Wales Hospital, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR.

Hong Kong Cancer Institute, State Key Laboratory of Translational Oncology, The Chinese University of Hong Kong, Hong Kong SAR.

出版信息

Data Brief. 2020 Mar 12;30:105421. doi: 10.1016/j.dib.2020.105421. eCollection 2020 Jun.

DOI:10.1016/j.dib.2020.105421
PMID:32215313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7091229/
Abstract

Chemotherapy-induced nausea and vomiting (CINV) are highly distressing symptoms for cancer patients undergoing cytotoxic chemotherapy. This dataset was obtained from a homogenous group of Chinese breast cancer patients who were uniformly planned to receive a highly emetogenic (neo)adjuvant chemotherapy regimen, consisting of doxorubicin and cyclophosphamide (commonly known as AC). Patients were being randomized to one of the two antiemetic regimens: aprepitant, ondansetron and dexamethasone with (the Olanzapine arm) or without olanzapine (the Standard arm). Patients underwent self-reported diaries and questionnaires to record their nausea and vomiting symptoms, use of rescue medication as well as their quality of life (QOL). The primary and secondary endpoints have focused on efficacy analysis during the first cycle of AC chemotherapy; the results have been reported in The Breast [1]. In this Data in Brief article, we provide outcome of the analysis of data collected during multiple cycles of chemotherapy. The data reported here include the proportion of patients with "Complete Response", "Complete Protection" and "Total Control" of emesis in the acute (0-24 h), delayed (24-120 h) and overall periods (0-120 h), as well as QOL data during all the 4 cycles of AC.

摘要

化疗引起的恶心和呕吐(CINV)是接受细胞毒性化疗的癌症患者极为痛苦的症状。该数据集来自一组同质的中国乳腺癌患者,这些患者均计划接受由阿霉素和环磷酰胺(俗称AC)组成的高度致吐性(新)辅助化疗方案。患者被随机分为两种止吐方案之一:阿瑞匹坦、昂丹司琼和地塞米松联合奥氮平(奥氮平组)或不联合奥氮平(标准组)。患者通过自我报告的日记和问卷来记录他们的恶心和呕吐症状、急救药物的使用以及他们的生活质量(QOL)。主要和次要终点集中在AC化疗第一个周期的疗效分析上;结果已在《乳腺癌》杂志上发表[1]。在这篇《简要数据》文章中,我们提供了多周期化疗期间收集数据分析的结果。这里报告的数据包括在急性(0 - 24小时)、延迟(24 - 120小时)和整个期间(0 - 120小时)呕吐“完全缓解”、“完全预防”和“完全控制”的患者比例,以及AC化疗所有4个周期的生活质量数据。