Chemotherapy induced emesis: pathophysiology and prevention

被引:3
|
作者
Mailliez, A. [1 ]
Bonneterre, J. [1 ]
机构
[1] Ctr Oscar Lambret, Dept Senol, F-59000 Lille, France
关键词
anti-emetic therapy; 5-HT3 serotonin receptor antagonists; NK1 receptor antogonists; steroids; anti-emetic guidelines; CISPLATIN-INDUCED EMESIS; MODERATELY EMETOGENIC CHEMOTHERAPY; ORAL NEUROKININ-1 ANTAGONIST; 5-HT3 RECEPTOR ANTAGONIST; PLACEBO-CONTROLLED TRIAL; HIGH-DOSE METOCLOPRAMIDE; PHASE-II TRIAL; INDUCED NAUSEA; DOUBLE-BLIND; RANDOMIZED CROSSOVER;
D O I
10.1684/bdc.2009.0979
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nausea and emesis are one of the most feared secondary effect of chemotherapy. The development of antiemetic therapies has increased after the introduction of cisplatin, a cytotoxin with the highest emetic potential. Chemotherapy-induced nausea and vomiting (CINV) have been classified into acute, delayed and anticipatory based on the time of onset. According to the percentage of nausea and emesis without any antiemetic treatment, chemotherapy is divised into highly, moderate, low and very low emetic potential. The discovery of emetics stimuli neurotransmitters and their receptors has led to the introduction of new molecules which associated with steroids have prevented nausea and vomiting chemotherapy-induced for 70 to 80% of the patients receiving chemotherapy with high emetic potential. Numerous studies have evaluated the various antiemetics and recommendations were issued by learned societies in US and Europe. This text discusses the physiopathology of nausea and vomiting, the development of anti-emetics and the new discovered antiemetics. Finally, a synthesis of the recommandations from the guidelines developed by the Multinational Association of Supportive Care in Cancer (MASCC), the American Society of Clinical Oncology (ASCO), the National Comprehensive Cancer Network (NCCN) and the European Society for Medical Oncology (ESMO) is presented. triangle
引用
收藏
页码:233 / 243
页数:11
相关论文
共 50 条
  • [1] DEXAMETHASONE IN THE PREVENTION OF CHEMOTHERAPY INDUCED EMESIS
    HOLOYE, P
    SCHRECK, I
    KALBFLEISCH, J
    [J]. PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, 1983, 24 (MAR): : 162 - 162
  • [2] Pathophysiology of chemotherapy-induced Versus non-chemotherapy-induced emesis
    Holzer, P.
    [J]. ONKOLOGIE, 2013, 36 : 90 - 90
  • [3] Drug utilization for prevention of chemotherapy (CT)-induced emesis
    Roila, F
    Ballatori, E
    Palmiotti, G
    Epifani, C
    Antimi, M
    Catalano, G
    Cruciani, G
    Amici, S
    Tonato, M
    [J]. EUROPEAN JOURNAL OF CANCER, 1997, 33 : 69 - 69
  • [4] CONTINUOUS INFUSION OF METOCLOPRAMIDE FOR PREVENTION OF CHEMOTHERAPY-INDUCED EMESIS
    AGOSTINUCCI, WA
    GANNON, RH
    SCHAUER, PK
    WALTERS, JK
    [J]. CLINICAL PHARMACY, 1986, 5 (02): : 150 - 153
  • [5] PREVENTION OF CHEMOTHERAPY-INDUCED EMESIS - THE STATE-OF-THE-ART
    ROILA, F
    TONATO, M
    DELFAVERO, A
    [J]. DIGESTIVE DISEASES, 1993, 11 (06) : 343 - 353
  • [6] Tropisetron in the prevention of chemotherapy-induced acute emesis in pediatric patients
    Uysal, KM
    Olgun, N
    Sanalioglu, F
    [J]. TURKISH JOURNAL OF PEDIATRICS, 1999, 41 (02) : 207 - 218
  • [7] Prevention of delayed emesis caused by chemotherapy
    Gopur, MS
    Ledakis, P
    Norvell, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (12): : 888 - 889
  • [8] Effectiveness of antiemetic drugs in prevention of chemotherapy (CT)-induced acute emesis
    DeAngelis, V
    Ciccarese, G
    Alessandroni, P
    Cattaneo, MT
    Agostara, B
    Atzeni, M
    Dionisi, S
    DiCostanzo, F
    Troccoli, G
    [J]. EUROPEAN JOURNAL OF CANCER, 1997, 33 : 57 - 57
  • [9] THE CLINICAL ROLE OF GRANISETRON (KYTRIL) IN THE PREVENTION OF CHEMOTHERAPY-INDUCED EMESIS
    PEREZ, EA
    GANDARA, DR
    [J]. SEMINARS IN ONCOLOGY, 1994, 21 (03) : 15 - 21
  • [10] PREVENTION OF CHEMOTHERAPY-INDUCED EMESIS WITH GRANISETRON IN CHILDREN WITH MALIGNANT DISEASES
    MIYAJIMA, Y
    NUMATA, S
    KATAYAMA, I
    HORIBE, K
    [J]. AMERICAN JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1994, 16 (03): : 236 - 241