A meta-analysis of olanzapine for the prevention of chemotherapy-induced nausea and vomiting.

Sci Rep

Department of pulmonary Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, 200030, Shanghai, China.

Published: April 2014

AI Article Synopsis

  • Chemotherapy-induced nausea and vomiting (CINV) can significantly impact patients' quality of life, leading to treatment discontinuation.
  • Olanzapine, typically used as an atypical antipsychotic, has shown effectiveness in managing refractory CINV by targeting multiple receptors involved in nausea pathways.
  • A meta-analysis of 6 studies with 726 patients indicated that including olanzapine in antiemetic regimens is more effective at reducing CINV, particularly in the delayed phase, for both general and Chinese populations.

Article Abstract

Chemotherapy-induced nausea and vomiting (CINV) is associated with a significant deterioration in quality of life and is one of the reasons for the discontinuation of treatment. Olanzapine is known as an atypical antipsychotic agent, but it has been reported to be effective in treating refractory CINV due to its broad and potent inhibitory activity at multiple receptors involved in the nausea and vomiting pathways. This study was conducted to assess the efficacy of olanzapine for the prevention of CINV after moderately or highly emetogenic chemotherapy. After a search of Medline (Ovid), PubMed, CNKI, Wanfang and Weipu from 1990 to October 2013, all randomised controlled trials of olanzapine for the prevention of CINV were included in this study. The meta-analysis was performed using RevMan 5.0.19 software. 6 studies involving 726 total patients were included, of which 441 were Chinese oncology patients. We found that for both general populations and Chinese populations, antiemetic regimens including olanzapine are more effective at reducing CINV than regimens that do not include olanzapine, especially in the delayed phase of CINV.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381218PMC
http://dx.doi.org/10.1038/srep04813DOI Listing

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