2016 updated MASCC/ESMO consensus recommendations: prevention of nausea and vomiting following multiple-day chemotherapy, high-dose chemotherapy, and breakthrough nausea and vomiting

被引:87
作者
Einhorn, Lawrence H. [1 ]
Rapoport, Bernardo [2 ]
Navari, Rudolph M. [3 ]
Herrstedt, Jorn [4 ]
Brames, Mary J. [1 ]
机构
[1] Indiana Univ, Div Hematol Oncol, Simon Canc Ctr, 535 Barnhill Dr, Indianapolis, IN 46202 USA
[2] Med Oncol Ctr Rosebank, 129 Oxford Rd, ZA-2196 Johannesburg, South Africa
[3] 4518 Crown Point Lane, Mt Olive, AL 35117 USA
[4] Odense Univ Hosp, Dept Oncol, DK-5000 Odense, Denmark
关键词
CINV; Multiple-day chemotherapy; High-dose chemotherapy; Breakthrough nauseas and vomiting; NK1 receptor antagonists; 5-HT3 receptor antagonists; STEM-CELL TRANSPLANTATION; DAY CISPLATIN CHEMOTHERAPY; EMETOGENIC CHEMOTHERAPY; COMBINATION CHEMOTHERAPY; ANTAGONIST APREPITANT; RECEPTOR ANTAGONIST; ANTIEMETIC THERAPY; DOUBLE-BLIND; DEXAMETHASONE; PALONOSETRON;
D O I
10.1007/s00520-016-3449-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
This review summarizes the recommendations for the prophylaxis of acute and delayed nausea and vomiting induced by multiple-day chemotherapy, high-dose chemotherapy, and breakthrough nausea and vomiting as agreed at the MASCC/ESMO Antiemetic Guidelines update meeting in Copenhagen in June 2015. A systematic literature search using PubMed from January 01, 2009 through January 06, 2015 with a restriction to papers in English was conducted. There were three phase III randomized trials in patients undergoing high-dose chemotherapy and stem cell transplant and eight single arm non-randomized clinical studies (single in patients undergoing transplantation and one in patients receiving multiple-day chemotherapy treatment). We used a total of two randomized clinical trials in this guideline update. For patients receiving treatment for breakthrough chemotherapy-induced nausea and vomiting, a phase III randomized trial investigating the use of olanzapine versus metoclopramide in patients receiving highly emetogenic chemotherapy and a second single arm study looking at the effectiveness of olanzapine were identified. It was concluded that for patients receiving high-dose chemotherapy with stem cell transplant, a combination of a 5-HT3 receptor antagonist with dexamethasone and aprepitant (125 mg orally on day 1 and 80 mg orally on days 2 to 4) is recommended before chemotherapy. For patients undergoing multiple-day chemotherapy-induced nausea and vomiting, a 5-HT3 receptor antagonist, dexamethasone, and aprepitant, are recommended before chemotherapy for the prophylaxis of acute emesis and delayed emesis. For patients experiencing breakthrough nausea and vomiting, the available evidence suggests the use of 10 mg oral olanzapine, daily for 3 days. Mild to moderate sedation in this patient population (especially elderly patients) is a potential problem with this agent.
引用
收藏
页码:303 / 308
页数:6
相关论文
共 30 条
[1]
Randomized, Double-Blind, Placebo-Controlled, Phase III Cross-Over Study Evaluating the Oral Neurokinin-1 Antagonist Aprepitant in Combination With a 5HT3 Receptor Antagonist and Dexamethasone in Patients With Germ Cell Tumors Receiving 5-Day Cisplatin Combination Chemotherapy Regimens: A Hoosier Oncology Group Study [J].
Albany, Costantine ;
Brames, Mary J. ;
Fausel, Christopher ;
Johnson, Cynthia S. ;
Picus, Joel ;
Einhorn, Lawrence H. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (32) :3998-4003
[2]
Aprepitant for the control of delayed nausea and vomiting associated with the use of high-dose melphalan for autologous peripheral blood stem cell transplants in patients with multiple myeloma: a phase II study [J].
Bechtel, Thomas ;
McBride, Ali ;
Crawford, Brooke ;
Bullington, Susan ;
Hofmeister, Craig C. ;
Benson, Don M., Jr. ;
Jaglowski, Samantha ;
Penza, Sam ;
Andritsos, Leslie A. ;
Devine, Steven M. .
SUPPORTIVE CARE IN CANCER, 2014, 22 (11) :2911-2916
[3]
Chanthawong Suthan, 2014, Journal of the Medical Association of Thailand, V97, P349
[4]
The prevalence of avascular necrosis in patients treated with chemotherapy for testicular tumours [J].
Cook, AM ;
Dzik-Jurasz, ASK ;
Padhani, AR ;
Norman, A ;
Huddart, RA .
BRITISH JOURNAL OF CANCER, 2001, 85 (11) :1624-1626
[5]
The NK1 receptor antagonist aprepitant does not alter the pharmacokinetics of high-dose melphalan chemotherapy in patients with multiple myeloma [J].
Egerer, Gerlinde ;
Eisenlohr, Kathrin ;
Gronkowski, Martina ;
Burhenne, Juergen ;
Riedel, Klaus-Dieter ;
Mikus, Gerd .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 70 (06) :903-907
[6]
Palonosetron plus dexamethasone for prevention of chemotherapy-induced nausea and vomiting in patients receiving multiple-day cisplatin chemotherapy for germ cell cancer [J].
Einhorn, Lawrence H. ;
Brames, Mary J. ;
Dreicer, Robert ;
Nichols, Craig R. ;
Cullen, Michael T., Jr. ;
Bubalo, Joseph .
SUPPORTIVE CARE IN CANCER, 2007, 15 (11) :1293-1300
[7]
Antiemetic therapy for multiple-day chemotherapy and additional topics consisting of rescue antiemetics and high-dose chemotherapy with stem cell transplant: review and consensus statement [J].
Einhorn, Lawrence H. ;
Grunberg, Steven M. ;
Rapoport, Bernardo ;
Rittenberg, Cynthia ;
Feyer, Petra .
SUPPORTIVE CARE IN CANCER, 2011, 19 :S1-S4
[8]
Antiemetic therapy for multiple-day chemotherapy and high-dose chemotherapy with stem cell transplant: review and consensus statement [J].
Einhorn, LH ;
Rapoport, B ;
Koeller, J ;
Grunberg, SM ;
Feyer, P ;
Rittenberg, C ;
Aapro, M .
SUPPORTIVE CARE IN CANCER, 2005, 13 (02) :112-116
[9]
ONDANSETRON - A NEW ANTIEMETIC FOR PATIENTS RECEIVING CISPLATIN CHEMOTHERAPY [J].
EINHORN, LH ;
NAGY, C ;
WERNER, K ;
FINN, AL .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (04) :731-735
[10]
ONDANSETRON VERSUS ONDANSETRON, DEXAMETHASONE, AND CHLORPROMAZINE IN THE PREVENTION OF NAUSEA AND VOMITING ASSOCIATED WITH MULTIPLE-DAY CISPLATIN CHEMOTHERAPY [J].
FOX, SM ;
EINHORN, LH ;
COX, E ;
POWELL, N ;
ABDY, A .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (12) :2391-2395