Abstract | BACKGROUND: METHODS: A nested case-control analysis was conducted within a cohort of 27 992 patients of Clalit Health Services, newly treated with a tyrosine kinase-targeting, and/or chemotherapeutic drug, for a malignant disease, between 1 January 2005 and 31 December 2012. Each new case of HF was matched to up to 30 controls from the cohort on calendar year of cohort entry, age, gender, and duration of follow-up. Main outcome measure was odds ratio (OR) with 95% confidence interval (CI) of new-onset HF. RESULTS: There were 936 incident cases of HF during 71 742 person-years of follow-up. Trastuzumab (OR 1.90, 95% CI 1.46-2.49), cetuximab (OR 1.72, 1.10-2.69), panitumumab (OR 3.01, 1.02-8.85), and sunitinib (OR 3.39, 1.78-6.47) were associated with increased HF risk. Comorbidity independently associated with higher risk in a multivariable conditional regression model was diabetes mellitus, hypertension, chronic renal failure, ischaemic heart disease, valvular heart disease, arrhythmia, and smoking. CONCLUSIONS:
|
Authors | N Gronich, I Lavi, O Barnett-Griness, W Saliba, D R Abernethy, G Rennert |
Journal | British journal of cancer
(Br J Cancer)
Vol. 116
Issue 10
Pg. 1366-1373
(May 09 2017)
ISSN: 1532-1827 [Electronic] England |
PMID | 28399109
(Publication Type: Journal Article)
|
Chemical References |
- Antibodies, Monoclonal
- Antineoplastic Agents
- Indoles
- Protein Kinase Inhibitors
- Pyrroles
- Panitumumab
- Trastuzumab
- Cetuximab
- Sunitinib
|
Topics |
- Aged
- Aged, 80 and over
- Antibodies, Monoclonal
(adverse effects)
- Antineoplastic Agents
(adverse effects)
- Case-Control Studies
- Cetuximab
(adverse effects)
- Cohort Studies
- Heart Failure
(epidemiology)
- Humans
- Incidence
- Indoles
(adverse effects)
- Israel
(epidemiology)
- Middle Aged
- Neoplasms
(drug therapy)
- Odds Ratio
- Panitumumab
- Protein Kinase Inhibitors
(adverse effects)
- Pyrroles
(adverse effects)
- Risk Factors
- Sunitinib
- Trastuzumab
(adverse effects)
|