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Original Article
Association between Antipsychotic Drug and Survival in Patients with Lung Cancer Treated with Chemoradiotherapy: A Nationwide Korean Cohort Study
Dong-Yun Kim1,2orcid , In Gyu Hwang3, Sun Mi Kim4, Dae Ryong Kang5,6, Tae-Hwa Go5, Se Hwa Hong5, Shin Young Park7, Hyunho Lee7, Jin Hwa Choi1,2orcid

DOI: https://doi.org/10.4143/crt.2024.554 [Accepted]
Published online: February 6, 2025
1Department of Radiation Oncology, Chung-Ang University Hospital, Seoul, Korea
2Department of Radiation Oncology, Chung-Ang University College of Medicine, Seoul, Korea
3Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea
4Department of Psychiatry, Chung-Ang University College of Medicine, Seoul, Korea
5Department of Medical Informatics and Biostatistics, Yonsei University Wonju College of Medicine, Wonju, Korea
6Department of Precision Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea
7Anticancer Strategy Research Institute, VSPharmTech Co., Ltd., Seoul, Korea
Corresponding author:  Jin Hwa Choi
Tel: 82-2-6299-2676 
Email: bonnybee@cau.ac.kr
Received: 12 June 2024   • Accepted: 5 February 2025
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Purpose
Antipsychotic drugs (APDs) can be used to relieve psychological symptoms in patients with cancer. We investigated the nationwide use of APDs during concurrent chemoradiotherapy (CCRT) for patients with lung cancer and its association with overall survival (OS).
Materials and Methods
The National Health Service database was used in this retrospective cohort study. Patients diagnosed with lung cancer between 2010 and 2020 who received cisplatin-based CCRT were included. The APDs included in the analysis were aripiprazole, quetiapine, olanzapine, risperidone, haloperidol, and chlorpromazine, and the APD prescription details included prescription time, dosage, and duration.
Results
Among the 23,099 patients with lung cancer treated with CCRT, 2,662 (11.5%) took APDs concurrently. Quetiapine (47.3%) and chlorpromazine (36.6%) were the frequently prescribed APDs. In the univariate analysis, patients prescribed APDs during CCRT had a significantly worse OS than those who did not take APDs. The 2-year OS rates for APD (+) and APD (-) patients were 20.4% and 36.4%, respectively (p < 0.001). Multivariable analyses revealed that APD prescription, male, age >80 years, and comorbidities, such as hypertension, myocardial infarction, and depressive disorder, significantly influenced OS. In patients who used APDs during CCRT, APD prescription timing (pre-CCRT vs. during CCRT), dosage (low vs. high) and duration (within 6 months vs. over 6 months) had no significant difference.
Conclusion
Overall, 11.5% of patients with lung cancer used APDs during CCRT. Patients who used APDs during CCRT had poorer survival than those who did not. Further studies are required to elucidate the effects of APDs on patients with cancer.

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