Literature DB >> 6098368

Advances in anti-emetic therapy.

M T Bakowski.   

Abstract

Evaluation of the activity of anti-emetic drugs in randomized controlled trials has, in most cases, demonstrated the superiority of treatment over placebo administration for the control of chemotherapy-induced emesis (see Table 15). The degree of control of emesis relates both to the intensity of the emetogenic stimulus and to the effectiveness of the anti-emetic agent employed. Prochlorperazine is a relatively weak anti-emetic. The drug exhibits modest activity in the treatment of emesis produced by mild emetogenic stimuli, but is relatively ineffective in the treatment of patients on moderate to severely emetogenic drugs. Domperidone has demonstrated activity against moderately emetogenic stimuli but has not been evaluated in cisplatin-treated patients. The cannabinoids have proved efficacious in the treatment of emesis induced by more severe emetogenic stimuli. THC therapy, however, has been limited in some studies by toxicity. High-dose metoclopramide has demonstrated efficacy in small series of patients in the treatment of cisplatin-induced vomiting. Dexamethasone activity as a single agent is in doubt but the drug may improve the efficacy of metoclopramide when used in combination. For the future, the use of combinations of anti-emetics with differing sites of action and non-overlapping toxicities, may lead to further improvement in efficacy. Combinations of centrally-acting drugs such as the cannabinoids plus dopamine antagonists such as metoclopramide or domperidone, are worth evaluating. The control of anticipatory nausea and vomiting is another major area of interest which has, as yet, not been studied in any depth. A single comparative trial has been reported in the literature (50) and in this study, behavioural therapy rather than drug therapy was evaluated. There may be a place for the evaluation of behavioural therapy in combination with drugs exhibiting anxiolytic properties such as the benzodiazepines and the cannabinoids. Finally, new anti-emetic drugs with an improved therapeutic index will be welcomed by the patient.

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Year:  1984        PMID: 6098368     DOI: 10.1016/0305-7372(84)90010-0

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  8 in total

1.  Antiemetic study design: desirable objectives, stratifications and analyses.

Authors:  I N Olver
Journal:  Br J Cancer Suppl       Date:  1992-12

2.  Anti-Inflammatory Agents for Cancer Therapy.

Authors:  Elizabeth R Rayburn; Scharri J Ezell; Ruiwen Zhang
Journal:  Mol Cell Pharmacol       Date:  2009

3.  Comparison of antiemetic efficacy of domperidone, metoclopramide, and dexamethasone in patients receiving outpatient chemotherapy regimens.

Authors:  D Cunningham; C Evans; J C Gazet; H Ford; A Pople; J Dearling; D Chappell; C Coombes
Journal:  Br Med J (Clin Res Ed)       Date:  1987-07-25

4.  Prospective randomized double-blind trial of nabilone versus domperidone in the treatment of cytotoxic-induced emesis.

Authors:  M Pomeroy; J J Fennelly; M Towers
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

5.  Methodology and assessment in clinical anti-emetic research: a meta-analysis of outcome parameters.

Authors:  G R Morrow
Journal:  Br J Cancer Suppl       Date:  1992-12

6.  A randomized trial of the effects of pharmacist intervention on the cost of antiemetic therapy with ondansetron.

Authors:  G Dranitsaris; D Warr; A Puodziunas
Journal:  Support Care Cancer       Date:  1995-05       Impact factor: 3.603

Review 7.  Chemotherapy induced emesis--mechanisms and treatment: a review.

Authors:  C M Edwards
Journal:  J R Soc Med       Date:  1988-11       Impact factor: 18.000

8.  Efficacy of promethazine suppositories dispensed to outpatient surgical patients.

Authors:  C D Wright; J Jilka; W B Gentry
Journal:  Yale J Biol Med       Date:  1998 Sep-Oct
  8 in total

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