Abstract 463P
Background
Delirium represents global brain dysfunction caused by an underlying medical condition. In cancer, it is associated with worse outcome. Antipsychotic medications have been widely used, however evidence in cancer populations is still limited with concern of potential adverse effects.
Methods
A comprehensive search was conducted among PubMed, EMBASE, Science Direct, and Scopus. Keywords used in this systematic review were antipsychotic agents, delirium, and neoplasm. Publications were limited to English manuscripts published in the last 15 years. Quality of each studies were assessed with Newcastle-Ottawa Scale (NOS).
Results
This review included 11 studies with a total of 1,896 patients aged 23 to 99. The cancer types varied and included lungs, gastrointestinal, hepatobiliary, urological, breast, head and neck, pancreas, lymphoma, sarcoma, and skin cancers. Some studies involved patients with brain metastasis and central nervous system lesions. These studies covered different cancer stages, including advanced, terminal, and localized. The antipsychotic medications examined in this review were haloperidol, quetiapine, chlorpromazine/levomepromazine, olanzapine, risperidone, trazodone, aripiprazole, and perospirone. Both typical and atypical antipsychotics were found to be similarly effective in managing delirium, but typical antipsychotics were associated with a higher prevalence of extrapyramidal symptoms. Higher antipsychotic doses were linked to increased mortality in cancer patients with delirium. Delirium outcomes were assessed using scales such as the Memorial Delirium Assessment Scale (MDAS), Richmond Agitation-Sedation Scale Palliative version (RASS-PAL), and others. Adverse events included hypotension, hypokinesia, sedation, extrapyramidal symptoms, falls, aspiration pneumonia, and urinary retention. Notably, no deaths were reported as a result of antipsychotic therapy.
Conclusions
Antipsychotic interventions to manage delirium in cancer patients consistently showed positive effects in addressing immediate distress and become a meaningful component of end-of-life support.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
551P - Real-world incidence and outcomes of immune-related adverse events in NSCLC patients
Presenter: Andrea Knox
Session: Poster Display
Resources:
Abstract
552P - TROPION-Lung05: Datopotamab deruxtecan (Dato-DXd) in Asian patients (pts) with previously treated non-small cell lung cancer (NSCLC) with actionable genomic alterations (AGAs)
Presenter: Yasushi Goto
Session: Poster Display
Resources:
Abstract
553P - Preceding plasma EGFR vs upfront tissue NGS for advanced NSCLC in the Chinese population: A single centre experience in Hong Kong
Presenter: Janet Du
Session: Poster Display
Resources:
Abstract
554P - Comparison of the analytical performance of endobronchial ultrasound-guided transbronchial needle aspiration and other sampling methods for the Oncomine Dx target test: An observational study
Presenter: Kazuhito Miyazaki
Session: Poster Display
Resources:
Abstract
555P - Quality of life in patients with stage IV non-small cell lung cancer and the influence of druggable mutations over time: A prospective, territory-wide study in Hong Kong
Presenter: Jason C S Ho
Session: Poster Display
Resources:
Abstract
556P - Results from the phase I study on efficacy and safety of iruplinalkib (WX-0593) for anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC) patients who received prior second-generation ALK tyrosine kinase inhibitors (TKIs)
Presenter: xuezhi Hao
Session: Poster Display
Resources:
Abstract
557P - Longitudinal plasma proteomic profiling of EML4-ALK positive lung cancer receiving ALK-TKIs therapy
Presenter: Shasha Wang
Session: Poster Display
Resources:
Abstract
558P - Treatment duration and adherence of brigatinib as second-line treatment after crizotinib for ALK+ NSCLC in South Korea
Presenter: Jeong Eun Lee
Session: Poster Display
Resources:
Abstract
559P - Comprehensive survey of AACR GENIE database revealed a wide range of TMB distribution among all three classes (I, II, III) of BRAF mutated NSCLC
Presenter: Zhaohui Arter
Session: Poster Display
Resources:
Abstract
560P - Triple-targeted therapy of dabrafenib, trametinib and osimertinib for the treatment of acquired BRAF V600E mutation after progression on EGFR-TKIs in advanced EGFR-mutant NSCLC
Presenter: Chengdi Weng
Session: Poster Display
Resources:
Abstract