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Updated: May 9, 2025

Assessment of Resistance to Tyrosine Kinase Inhibitors by an Interrogation of Signal Transduction Pathways by Antibody Arrays
Published on: September 19, 2018
Olanzapine for Managing Side Effects From Antiangiogenic Tyrosine-Kinase Inhibitors
Regina M Koch1, Miguel Muniz2, Candy S Peskey2
1Department of Internal Medicine (R.M.K.,), Mayo Clinic, Rochester, Minnesota, USA.
Context:
Side effects from tyrosine kinase inhibitors (TKIs) are common and burdensome. Olanzapine is useful for managing symptoms from conventional chemotherapy, but its role in treating TKI-related side effects is unclear.
Objectives:
Examine the efficacy of olanzapine for TKI-induced nausea, vomiting, anorexia, weight loss, and insomnia.
Methods:
All patients prescribed olanzapine with lenvatinib, cabozantinib, axitinib, or tivozanib at Mayo Clinic between January 2018 and June 2024 were assessed for inclusion. For baseline assessment, clinical notes documenting symptoms and indication(s) for starting olanzapine were reviewed. Notes and portal messages from the first three months after starting olanzapine were then evaluated for qualitative descriptions of change in symptom burden. Data were categorized as "improved," "worsened," "stable," or "missing data," with each symptom domain analyzed independently, when olanzapine was prescribed for multiple interrelated symptoms.
Results:
Sixty patients received olanzapine, most commonly 5 mg (n = 37, 61.7%) or 2.5 mg (n = 16, 26.6%). Indications included nausea without vomiting (n = 35), anorexia (n = 25), nausea with vomiting (n = 16), weight loss (n = 16), and insomnia (n = 11). It was given for multiple symptoms in 32 patients. Within the first 3 months, 85% of patients had improvement in nausea without vomiting, 93% in nausea with vomiting, 74% in appetite, and 85% in sleep. Among 34 patients with weight loss prior to olanzapine, 50% gained weight (median: 6.1 kg), 26% stabilized (±1 kg), and 24% continued to lose weight. Only 4 patients discontinued olanzapine due to side effects.
Conclusion:
Olanzapine appears effective in treating TKI-induced nausea, vomiting, anorexia, insomnia, and weight loss, warranting further investigation in prospective studies.
Insights
Olanzapine effectively manages side effects from tyrosine kinase inhibitors (TKIs), including nausea, vomiting, anorexia, and insomnia. This study suggests olanzapine is a promising treatment for these burdensome TKI-induced symptoms.
Area of Science:
- Oncology
- Pharmacology
- Clinical Medicine
Background:
- Tyrosine kinase inhibitors (TKIs) commonly cause burdensome side effects.
- Olanzapine is used for chemotherapy-induced symptoms, but its efficacy for TKI side effects is not well-established.
Purpose of the Study:
- To evaluate the effectiveness of olanzapine in managing TKI-induced nausea, vomiting, anorexia, weight loss, and insomnia.
Main Methods:
- Retrospective review of 60 patients treated with olanzapine and TKIs (lenvatinib, cabozantinib, axitinib, tivozanib) at Mayo Clinic.
- Clinical notes were analyzed for symptom changes (improved, worsened, stable) within three months of initiating olanzapine.
Main Results:
- High rates of improvement were observed: 85% for nausea without vomiting, 93% for nausea with vomiting, 74% for appetite, and 85% for sleep.
- Of patients with prior weight loss, 50% gained weight, and 26% stabilized.
- Only 4 patients discontinued olanzapine due to side effects.
Conclusions:
- Olanzapine demonstrates significant efficacy in alleviating common side effects associated with tyrosine kinase inhibitor therapy.
- Further prospective studies are recommended to confirm these findings and establish olanzapine as a standard treatment option.
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