TY - JOUR
T1 - beta-Blocker use and all-cause mortality of melanoma patients: Results from a population-based Dutch cohort study
AU - Livingstone, E
AU - Zandwijk - Hollestein, Loes
AU - van Herk-Sukel, MPP
AU - van de Poll-Franse, L
AU - Nijsten, Tamar
AU - Schadendorf, D
AU - Vries, Esther
PY - 2013
Y1 - 2013
N2 - Background: Results from preclinical and observational studies suggest that beta-adrenoreceptor inhibition might influence disease progression of melanoma. Patients and methods: Patients >= 18 years with cutaneous melanoma (Breslow thickness > 1 mm) registered in the Eindhoven Cancer Registry between January 1, 1998 and December 31, 2010, who were also registered with PHARMO record linkage system (RLS), were eligible. Randomly selected patients using beta-blockers from PHARMO record linkage system (RLS) matched on age and gender served as a control cohort. Adjusted time-dependent and time-fixed Cox proportional hazard models were employed to estima Results: 203 of 709 eligible patients used beta-blockers after melanoma diagnosis. The use of beta-blockers was not associated with the risk of dying (adjusted hazard ratio (HR) 0.82, 95% confidence interval (CI) 0.55-1.24). Neither duration of exposure nor beta-blocker dosage showed significant influence on survival. Five-year relative survival for beta-blocker users was lower than in non-users amongst melanoma patients (80.9% and 83.7%, respectively) but higher among the beta-blocker control g Conclusion: Our results do not show a statistically significant impact of beta-blocker exposure on overall survival of melanoma patients, regardless of the timing, duration or dosage of beta-blocker use. (C) 2013 Elsevier Ltd. All rights reserved.
AB - Background: Results from preclinical and observational studies suggest that beta-adrenoreceptor inhibition might influence disease progression of melanoma. Patients and methods: Patients >= 18 years with cutaneous melanoma (Breslow thickness > 1 mm) registered in the Eindhoven Cancer Registry between January 1, 1998 and December 31, 2010, who were also registered with PHARMO record linkage system (RLS), were eligible. Randomly selected patients using beta-blockers from PHARMO record linkage system (RLS) matched on age and gender served as a control cohort. Adjusted time-dependent and time-fixed Cox proportional hazard models were employed to estima Results: 203 of 709 eligible patients used beta-blockers after melanoma diagnosis. The use of beta-blockers was not associated with the risk of dying (adjusted hazard ratio (HR) 0.82, 95% confidence interval (CI) 0.55-1.24). Neither duration of exposure nor beta-blocker dosage showed significant influence on survival. Five-year relative survival for beta-blocker users was lower than in non-users amongst melanoma patients (80.9% and 83.7%, respectively) but higher among the beta-blocker control g Conclusion: Our results do not show a statistically significant impact of beta-blocker exposure on overall survival of melanoma patients, regardless of the timing, duration or dosage of beta-blocker use. (C) 2013 Elsevier Ltd. All rights reserved.
U2 - 10.1016/j.ejca.2013.07.141
DO - 10.1016/j.ejca.2013.07.141
M3 - Article
C2 - 23942335
SN - 0959-8049
VL - 49
SP - 3863
EP - 3871
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 18
ER -