There is an increased risk of congestive heart failure (CHF) following anthracyclinebased chemotherapy in patients with Diffuse Large B-cell lymphoma (DLBCL). Little is known about risk factors of CHF, other cardiovascular events (CVE), and CVE effect on outcomes. We conducted a retrospective review of 463 newly diagnosed DLBCL patients treated between 2002 and 2016 with anthracycline containing regimens. At a median follow up of 71.3 months, 10.4% patients developed new CHF, 4.97% had new atrial fibrillation and 3.2% had new coronary artery disease. Age over 65, advanced stage DLBCL and diabetes were associated with increased cumulative incidence of CVE. Patients with prior diabetes had decreased progression-free survival and overall survival in comparison to non-diabetics. Patients who had a CVE in the first year had significant worse OS then patients who did not have a CVE (Hazard Ratio 10.0, 95% CI, 7.24-13.88). A risk score incorporating age at DLBCL diagnosis, baseline lymphocyte count, disease stage and diabetes stratified into groups with low, intermediate and high risk for CVE, with 1year cumulative incidence of CVE of 5.3%, 7.9% and 13.4%. Diffuse large B-cell lymphoma patients treated with anthracycline containing regimens have high incidence of CVE, which are not limited to CHF. Clinical variables at the time of diagnosis can identify the group of DLBCL patients at highest risk of CVE, for whom preventive interventions should be considered. K E Y W O R D S cardiac toxicity, cardiovascular events, diabetes, diffuse large B cell lymphoma
| INTRODUCTIONAnthracycline-containing chemoimmunotherapy can achieve high response rates and improve survival in diffuse large B-cell lymphoma (DLBCL), but can cause cardiovascular toxicity. There is an increased risk of congestive heart failure (CHF) following anthracycline treatment, with a dose dependent risk increase. 1,2 This understanding has led to recommended maximum cumulative doxorubicin (or equivalent) dose of 500 mg/m2, with doses frequently limited to 450 mg/m2 in clinical practice. 3 Despite dosing limits, a recent metaanalysis identified a pooled proportion for developing CHF of 4.62%. 4 When the analysis was limited to studies including post treatment cardiac evaluation, the pooled proportion was 11.7%. Cardiac toxicity was increased in studies where the median age was >65 years and including a larger proportion of women. Other than CHF, there are limited data regarding the risk of developing other types of