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Impact of CINV in earlier cycles on CINV and chemotherapy regimen modification in subsequent cycles in Asia Pacific clinical practice

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单位: [1]Catholic Univ Korea, St Vincents Hosp, Suwon, South Korea [2]Mackay Mem Hosp, Ctr Canc, Taipei, Taiwan [3]Natl Univ Singapore, Natl Canc Ctr Singapore, Singapore 117548, Singapore [4]Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Ctr Canc, Wuhan 430074, Peoples R China [5]Shanghai Chest Hosp, Dept Pulm Med, Shanghai, Peoples R China [6]Beijing Canc Hosp, Beijing, Peoples R China [7]OptumInsight Inc, Stockholm, Sweden [8]Merck Sharp & Dohme Ltd, Outcomes Res, Shanghai, Peoples R China [9]Merck Res Labs, Global Hlth Outcomes, Whitehouse Stn, NJ USA [10]Univ Adelaide, Fac Hlth Sci, Adelaide, SA, Australia
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关键词: Antiemetic Cancer Chemotherapy Nausea Observational Vomiting

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We sought to describe the impact of chemotherapy-induced nausea and vomiting (CINV) in prior cycles on CINV and chemotherapy regimen modification in subsequent cycles. Eligible patients in this multinational prospective observational study were adults (a parts per thousand yen18 years old) receiving their first single-day highly or moderately emetogenic chemotherapy (HEC or MEC). Multivariate logistic regression was used to assess the impact of CINV in prior cycles on CINV in subsequent cycles. Other independent variables included in the model were the cycle number, age, sex, and emetogenicity of regimen. There were 598 evaluable patients in cycle 2 and 533 in cycle 3, half receiving HEC and half MEC. Patients who experienced complete response (no emesis or rescue antiemetics) in earlier cycles, relative to those with no complete response, had an adjusted odds ratio (OR) of 5.9 (95 % confidence interval (CI), 4.14-8.50) for experiencing complete response in subsequent cycles. Prior CINV was a significant and consistent predictor of subsequent CINV for all CINV endpoints: for emesis, OR 12.7 (95 % CI, 8.47-18.9), for clinically significant nausea, OR 7.9 (95 % CI, 5.66-10.9), and for clinically significant nausea and/or vomiting, OR 7.2 (5.17-10.1). Modifications to chemotherapy were recorded for 26-29 % of patients in cycles 2 and 3, with CINV as the major reason for the modification for 5-9 % of these patients. CINV in prior cycles was a strong and consistent predictor of CINV in subsequent cycles, while the incidence of chemotherapy regimen modification due to CINV was low in individual cycles.

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出版当年[2014]版:
大类 | 3 区 医学
小类 | 2 区 卫生保健与服务 2 区 康复医学 4 区 肿瘤学
最新[2025]版:
大类 | 3 区 医学
小类 | 2 区 康复医学 3 区 卫生保健与服务 3 区 肿瘤学
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出版当年[2013]版:
Q1 REHABILITATION Q2 HEALTH CARE SCIENCES & SERVICES Q3 ONCOLOGY
最新[2023]版:
Q1 REHABILITATION Q2 HEALTH CARE SCIENCES & SERVICES Q2 ONCOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2013版] 出版当年五年平均 出版前一年[2012版] 出版后一年[2014版]

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第一作者单位: [1]Catholic Univ Korea, St Vincents Hosp, Suwon, South Korea
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