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Identification of optimal contemporary antiemetic prophylaxis for doxorubicin-cyclophosphamide chemotherapy in Chinese cancer patients: post-hoc analysis of 3 prospective studies

机译:中国癌症患者多肠素 - 环磷酰胺化疗的最佳当代抗预防性的鉴定:3次前瞻性研究后HOC分析

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摘要

Objective:Chemotherapy-induced nausea and vomiting(CINV)are common with doxorubicin-cyclophosphamide(AC)chemotherapy.Recommended antiemetic regimens incorporate neurokinin-1 receptor antagonist(NK1 RA),5-hydroxytryptamine type-3 receptor antagonist(5 HT3 RA),corticosteroid,and dopamine antagonists.This post-hoc analysis compared results of 3 prospective antiemetic studies conducted among Chinese breast cancer patients who received(neo)adjuvant AC,in order to identify optimal antiemetic prophylaxis.Methods:A total of 304 patients were included:Group 1,ondansetron/dexamethasone(D1);Group 2,aprepitant/ondansetron/dexamethasone(D1);Group 3,aprepitant/ondansetron/dexamethasone(D1–3);Group 4,aprepitant/ondansetron/dexamethasone(D1–3)/olanzapine;and Group 5,netupitant/palonosetron/dexamethasone(D1–3).Antiemetic efficacies of Groups 3,4,and 5 during cycle 1 of AC were individually compared with Group 1.In addition,emesis outcomes of patients in Groups 3 and 5,and those of Groups 2 and 3,were compared.Results:When comparing efficacies of a historical doublet(5 HT3 RA/dexamethasone)with triplet antiemetic regimens(NK1 RA/5 HT3 RA/dexamethasone)with/without olanzapine,complete response(CR)percentages and quality of life(QOL)in overall phase of cycle 1 AC were compared between Group 1 and the other groups:Group 1 vs.3,41.9%vs.38.3%(P=0.6849);Group 1 vs.4,41.9%vs.65.0%(P=0.0107);and Group 1 vs.5,41.9%vs.60.0%(P=0.0460).Groups 4 and 5 achieved a better QOL.When comparing netupitant-based(Group 3)with aprepitant-based(Group 5)triplet antiemetics,CR percentages were 38.3%vs.60.0%,respectively(P=0.0176);Group 5 achieved a better QOL.When comparing 1 day(Group 2)vs.3 day(Group 3)dexamethasone,CR percentages were 46.8%and 38.3%,respectively(P=0.3459);Group 3 had a worse QOL.Conclusions:Aprepitant-containing triplets were non-superior to doublet antiemetics.Netupitant-containing triplets and adding olanzapine to aprepitant-containing triplets were superior to doublets.Netupitant/palonosetron/dexamethasone was superior to aprepitant/ondansetron/dexamethasone.Protracted administration of dexamethasone provided limited additional benefit.

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  • 来源
    《癌症生物学与医学:英文版》 |2021年第003期|P.825-832|共8页
  • 作者单位

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong ChinaState Key Laboratory of Translational Oncology The Chinese University of Hong Kong Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Princess Margaret Hospital Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong China;

    Department of Clinical Oncology Prince of Wales Hospital Faculty of Medicine Hong Kong Cancer Institute Hong Kong ChinaState Key Laboratory of Translational Oncology The Chinese University of Hong Kong Hong Kong China;

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  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 肿瘤学;
  • 关键词

    Netupitant; palonosetron; aprepitant; olanzapine; NEPA; Asians;

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