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The relationship between statin administration timing and survival outcomes in patients with cancer receiving immune checkpoint blockade.
Wang, Zihan; See, Xin Ya; Chiang, Cho-Hung; Chang, Yu-Cheng; Hsia, Yuan Ping; Chiang, Cho-Hsien; Peng, Cheng-Ming; Chiang, Cho-Han.
Afiliación
  • Wang Z; Department of Human Development and Education, Harvard University, Cambridge, MA, USA.
  • See XY; Department of Medicine, Unity Hospital, Rochester Regional Health, Rochester, NY, USA.
  • Chiang CH; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Chang YC; Department of Medicine, Danbury Hospital, Danbury, CT, USA.
  • Hsia YP; Department of Family Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City, Taiwan.
  • Chiang CH; Department of Environmental and Occupational Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Peng CM; London School of Hygiene & Tropical Medicine, London, UK.
  • Chiang CH; School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
J Chemother ; : 1-6, 2023 Dec 08.
Article en En | MEDLINE | ID: mdl-38062978
OBJECTIVE: Statins have been demonstrated to improve outcomes in patients receiving immune checkpoint blockade (ICB). This study aimed to investigate whether the timing of statin administration influences the outcomes of patients receiving ICB. METHODS: We conducted a retrospective cohort study utilizing electronic health records from two tertiary referral centers in Taiwan. We compared the overall survival (OS) and progression-free survival (PFS) of patients who received statins before and after ICB initiation. RESULTS: We included 734 patients who received ICB. Among them, 606 were non-statin users, 76 started statins after ICB initiation, and 52 started statins before ICB initiation. Post-ICB statin users demonstrated significantly prolonged OS (median 37.6 versus 10.3 versus 11.3 months, p = 0.009) and PFS (median 10.5 versus 6.3 versus 5.6 months, p = 0.024) compared to pre-ICB statin and non-statin users. Statin use after ICB initiation had a reduced risk of all-cause mortality (HR, 0.65 [95% CI: 0.45-0.94], p = 0.022) and progressive disease (HR, 0.71 [95% CI: 0.53-0.95], p = 0.021) by approximately 30-35%, compared to non-statin users. However, statin use prior to ICB initiation did not affect the risk of all-cause mortality or progressive disease. Similar results were observed after controlling for potential cofounders such as age, sex, cancer stage, and cancer type. CONCLUSIONS: These findings suggest that initiating statin therapy after the initiation of ICB, regardless of indication, is associated with improved patient prognosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chemother Asunto de la revista: ANTINEOPLASICOS / TERAPIA POR MEDICAMENTOS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chemother Asunto de la revista: ANTINEOPLASICOS / TERAPIA POR MEDICAMENTOS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido