2017
DOI: 10.1016/j.critrevonc.2017.02.017
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Efficacy and safety of olanzapine for the prevention of chemotherapy-induced nausea and vomiting: A systematic review and meta-analysis

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Cited by 50 publications
(34 citation statements)
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“…We agree that severe QTc prolongation is not an acute risk with olanzapine monotherapy in children without other cardiac risk factors or QTc prolonging polypharmacy. However, in clinical oncology practice, many children are on concomitant QTc prolonging medications and may need a reference electrocardiogram, often available from their baseline medical work‐up . In terms of dosing, we agree that 0.1 mg/kg/dose (max: 10 mg/dose) is a reasonable rule of thumb, though dosage forms of oral and disintegrating tablets may limit the increments for dosing.…”
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confidence: 83%
“…We agree that severe QTc prolongation is not an acute risk with olanzapine monotherapy in children without other cardiac risk factors or QTc prolonging polypharmacy. However, in clinical oncology practice, many children are on concomitant QTc prolonging medications and may need a reference electrocardiogram, often available from their baseline medical work‐up . In terms of dosing, we agree that 0.1 mg/kg/dose (max: 10 mg/dose) is a reasonable rule of thumb, though dosage forms of oral and disintegrating tablets may limit the increments for dosing.…”
mentioning
confidence: 83%
“…Одним из наиболее заметных нежелательных эффектов оланзапина является седация, которая может снижать приверженность пациентов к терапии и создавать неудобства при проведении лечения, особенно -в амбулаторном режиме. По данным метаанализа [29], около 35% пациентов при применении оланзапина испытывают седацию/повышенную сонливость. Навари Р. М.…”
Section: краткие данные о профиле безопасности оланзапинаunclassified
“…Olanzapine, an antipsychotic agent, blocks multiple neurotransmitters: serotonin, at 5H2a, 5H2c, 5H3, and 5HT6 receptors, dopamine at D1, D2, D3, and D4 brain receptor, catecholamines at alpha 1 adrenergic receptors, acetylcholine at muscarinic receptors, and histamine at H1 receptors. 7 In previous studies, olanzapine has been demonstrated to be a safe and effective agent in improving cancer-related symptoms, including chemotherapy-induced nausea and vomiting (CINV), [7][8][9][10][11][12][13][14][15][16] cancer pain, 17,18 cancer-related anorexia, 19,20 and cachexia. 21 The efficacy of olanzapine in improving HRQoL of cancer patients was demonstrated in several studies as a secondary endpoint.…”
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confidence: 99%