5-HT3受体拮抗剂联合地塞米松预防化疗所致恶心呕吐的临床疗效

被引:17
作者
陈俊明 [1 ,2 ]
王涵 [1 ]
王洪学 [1 ]
黄金新 [3 ]
谭爱花 [1 ]
周文献 [1 ]
陆永奎 [1 ]
谢伟敏 [1 ]
机构
[1] 广西医科大学附属肿瘤医院乳腺及骨软组织肿瘤内科
[2] 广西医科大学研究生院
[3] 柳州市工人医院肿瘤科
关键词
5-HT3受体拮抗剂; 化疗; 恶心; 呕吐; 不良反应;
D O I
暂无
中图分类号
R730.53 [化学(药物)疗法];
学科分类号
100112 [医学生物化学与分子生物学];
摘要
目的探讨第一代5-羟色胺3受体拮抗剂(5-HT3RA)托烷司琼(Tropisetron,TRO)与第二代5-HT3RA帕洛诺司琼(Palonosetron,PAL)联合地塞米松预防化疗所致恶心和呕吐的疗效及安全性。方法选择2015年1月至2018年12月在广西医科大学附属肿瘤医院诊治,并接受含有高度催吐风险方案进行多日化疗的192例肿瘤患者为研究对象。采用随机、交叉自身对照法分为PAL组和TRO组,其中PAL组止吐方案为帕洛诺司琼联合地塞米松,TRO组为托烷司琼联合地塞米松方案。比较两组患者恶心、呕吐发生率及止吐药物相关不良反应发生率。结果 PAL组和TRO组患者在急性期(d1)的恶心和呕吐发生率差异均无统计学意义(均P>0.05),PAL组在延迟期(d2~5)及全程(d1~5)的恶心发生率均低于TRO组(均P<0.05),在延迟期(d3~d4)及全程呕吐的发生率亦低于TRO组(均P<0.05)。TRO组有57.3%的患者需重复使用5-HT3RA,高于PAL组的39.3%(P<0.05)。与止吐药物相关或可能相关的不良反应包括便秘、腹胀、头痛和呃逆等,两组不良反应发生率差异无统计学意义(P>0.05)。结论第二代5-HT3RA帕洛诺司琼防治延迟性化疗所致恶心和呕吐的疗效优于第一代5-HT3RA托烷司琼,安全性良好。
引用
收藏
页码:211 / 216
页数:6
相关论文
共 11 条
[1]
Effectiveness of Antiemetic Regimens for Highly Emetogenic Chemotherapy-Induced Nausea and Vomiting: A Systematic Review and Network Meta-Analysis [J].
Yokoe, Takamichi ;
Hayashida, Tetsu ;
Nagayama, Aiko ;
Nakashoji, Ayako ;
Maeda, Hinako ;
Seki, Tomoko ;
Takahashi, Maiko ;
Takano, Toshimi ;
Abe, Takayuki ;
Kitagawa, Yuko .
ONCOLOGIST, 2019, 24 (06) :E347-E357
[2]
Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update [J].
Hesketh, Paul J. ;
Kris, Mark G. ;
Basch, Ethan ;
Bohlke, Kari ;
Barbour, Sally Y. ;
Clark-Snow, Rebecca Anne ;
Danso, Michael A. ;
Dennis, Kristopher ;
Dupuis, L. Lee ;
Dusetzina, Stacie B. ;
Eng, Cathy ;
Feyer, Petra C. ;
Jordan, Karin ;
Noonan, Kimberly ;
Sparacio, Dee ;
Somerfield, Mark R. ;
Lyman, Gary H. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (28) :3240-+
[3]
2016 updated MASCC/ESMO consensus recommendations: prevention of nausea and vomiting following multiple-day chemotherapy, high-dose chemotherapy, and breakthrough nausea and vomiting [J].
Einhorn, Lawrence H. ;
Rapoport, Bernardo ;
Navari, Rudolph M. ;
Herrstedt, Jorn ;
Brames, Mary J. .
SUPPORTIVE CARE IN CANCER, 2017, 25 (01) :303-308
[4]
Three palonosetron regimens to prevent CINV in myeloma patients receiving multiple-day high-dose melphalan and hematopoietic stem cell transplantation [J].
Giralt, S. A. ;
Mangan, K. F. ;
Maziarz, R. T. ;
Bubalo, J. S. ;
Beveridge, R. ;
Hurd, D. D. ;
Mendoza, F. L. ;
Rubenstein, E. B. ;
DeGroot, T. J. ;
Schuster, M. W. .
ANNALS OF ONCOLOGY, 2011, 22 (04) :939-946
[5]
Daily Palonosetron Is Superior to Ondansetron in the Prevention of Delayed Chemotherapy-Induced Nausea and Vomiting in Patients With Acute Myelogenous Leukemia [J].
Mattiuzzi, Gloria N. ;
Cortes, Jorge E. ;
Blamble, Deborah A. ;
Bekele, Nebiyou ;
Xiao, Lianchun ;
Cabanillas, Maria ;
Borthakur, Gautam ;
Brien, Susan O. ;
Kantarjian, Hagop .
CANCER, 2010, 116 (24) :5659-5666
[6]
Palonosetron plus dexamethasone versus granisetron plus dexamethasone for prevention of nausea and vomiting during chemotherapy: a double-blind, double-dummy, randomised, comparative phase III trial [J].
Saito, Mitsue ;
Aogi, Kenjiro ;
Sekine, Ikuo ;
Yoshizawa, Hirohisa ;
Yanagita, Yasuhiro ;
Sakai, Hiroshi ;
Inoue, Kenichi ;
Kitogawa, Chiyoe ;
Ogura, Takashi ;
Mitsuhashi, Shoichi .
LANCET ONCOLOGY, 2009, 10 (02) :115-124
[7]
Palonosetron (Aloxi ? ) and dexamethasone for the prevention of acute and delayed nausea and vomiting in patients receiving multiple-day chemotherapy.[J].Maurizio Musso;Renato Scalone;Vincenza Bonanno;Alessandra Crescimanno;Vita Polizzi;Ferdinando Porretto;Carlo Bianchini;Tania Perrone.Supportive Care in Cancer.2009, 2
[8]
Improved prevention of moderately emetogenic chemotherapy‐induced nausea and vomiting with palonosetron; a pharmacologically novel 5‐HT<sub>3</sub> receptor antagonist.[J].Peter Eisenberg MD;Jazmin Figueroa‐Vadillo MD;Rosalio Zamora MD;Veena Charu MD;Julio Hajdenberg MD;Alan Cartmell MD;Alberto Macciocchi MD;Steven Grunberg MD.Cancer.2003, 11
[9]
肿瘤药物治疗相关恶心呕吐防治中国专家共识(2019年版) [J].
姜文奇 ;
巴一 ;
冯继锋 ;
史艳侠 ;
张俊 ;
沈波 ;
邢镨元 .
中国医学前沿杂志(电子版), 2019, 11 (11) :16-26
[10]
化疗所致恶心呕吐全程管理上海专家共识(2018年版) [J].
上海市抗癌协会癌症康复与姑息专业委员会 .
中国癌症杂志, 2018, 28 (12) :946-960