Effect of statins on the mortality of long-term survivors of nasopharyngeal carcinoma.
Abstract
e18084 Background: Despite the significant increase in five-year overall survival (OS) rate of patients with nasopharyngeal cancer (NPC) over the past few decades, long-term survivors remain at risk of excessive mortality and morbidity. Several population-based studies have suggested an association between statin use and a reduction in cancer morbidity and mortality. This territory-wide cohort study aims to investigate the relationship between statin use and mortality among the five-year survivors of NPC. Methods: This is a retrospective cohort study conducted with data from the Clinical Data Analysis Reporting System (CDARS), a previously validated territory-wide clinical information registry. Patients who survived 5 years after being diagnosed with non-metastatic NPC in Hong Kong between 1 January 1997 and 30 December 2015 were included in the analysis. Patients were divided into two groups: statin users and statin non-users. We performed the inverse propensity of treatment weighting (IPTW) method to balance confounding factors. The primary outcome of OS was compared between the two groups using the Kaplan-Meier method and stratified by the cause of death, statin types and duration of statin usage. Results: 8354 subjects (2598 statin users and 5756 statin non-users) were included in the final analysis. The mean age was 49.3±11.5 years, and 70.8% were male. Baseline characteristics were well balanced after adjustment by IPTW (SMD <0.10). The 10-year, 15-year, and 20-year survival probabilities of statin users compared to non-statin users were 88.4 vs. 70.9%, 76.1 vs. 54.1%, and 58.2 vs. 41.2% respectively (unadjusted HR: 0.49, 95% CI: 0.45-0.54, p<0.001, adjusted HR: 0.43, 95% CI: 0.36-0.52, p<0.001). Statin use was associated with reduced risk of death due to progressive or recurrence disease (HR: 0.74, p=0.039), secondary malignancy (HR: 0.48, p=0.008), cardiovascular disease (HR: 0.58, p=0.003), and pulmonary disease (HR: 0.57, p<0.001). The association of statin use and reduced mortality was duration-dependent. Mortality was significantly lower in long-term statin usage of > 6 years (HR: 0.47; 95% CI: 0.47-0.71, p<0.001) compared to short-term usage (3 months to 2 years). Type 2 statins were associated with a lower mortality compared with type 1 statins (HR: 0.50, 95% CI: 0.37-0.68, p<0.001). Conclusions: Our study suggests that statin usage is associated with reduced mortality in long-term NPC survivors. Further prospective study is warranted.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (17)
Ruyu Xu
Department of Clinical Oncology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China
Chi Leung Chiang
Department of Clinical Oncology, Centre of Cancer Medicine, School of Clinical Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong KongChina,
Philip Chun Ming Au
Department of Pharmacy and Pharmacology, The University of Hong Kong, Hong Kong, Hong Kong
Sik-Kwan Chan
Department of Clinical Oncology, The University of Hong Kong, Hong Kong, Hong Kong
Ka Shun Fong
Department of Clinical Oncology, The University of Hong Kong, Hong Kong, Hong Kong
James Chung Hang Chow
Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, Hong Kong
Ken Ka Man Cheung
Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, Hong Kong
Winnie Wing Yan Tin
Department of Clinical Oncology, Tuen Mun Hospital, Hong Kong, Hong Kong
Edwin Chun Yin Wong
Department of Clinical Oncology, Pamela Youde Nethersole Eastern Hospital, Hong Kong, Hong Kong
Tracy Tsz Shan Lau
Department of Oncology, Princess Margaret Hospital, Hong Kong, Hong Kong
Kenneth Chun Wai Wong
Department of Clinical Oncology, Prince of Wales Hospital, Hong Kong, Hong Kong
Ann Sum Yin Chan
Department of Clinical Oncology, Queen Mary Hospital, Hong Kong, Hong Kong
Victor Ho-fun Lee
Ian Chi Kei Wong
Anne Wing Mui Lee
Ching Lung Cheung
Department of Pharmacy and Pharmacology, The University of Hong Kong, Hong Kong, Hong Kong
CW Sing
Department of Clinical Oncology, University of Hong Kong, Hong Kong, Hong Kong