Key result
Lymphoma survivors treated with autologous stem-cell transplantation had a significantly higher risk of left ventricular systolic dysfunction than matched controls (OR 6.6; 95% CI 2.5-17.6; P<0.001).
Why the study?
Does prior treatment with auto-HCT for lymphoma increase the risk of left ventricular systolic dysfunction compared to matched controls?
Cross-Sectional (n=274)
Yes
Does prior treatment with auto-HCT for lymphoma increase the risk of left ventricular systolic dysfunction compared to matched controls?
Adult lymphoma survivors treated with auto-HCT have a significantly increased risk of left ventricular systolic dysfunction and heart failure compared to matched controls, driven by doxorubicin and cardiac radiation doses.
Answers are grounded in this paper and cite their sources.
Auto-HCT lymphoma survivors may warrant enhanced LV surveillance; Level 4 data leaves open causality and prevention.
PURPOSE: We aimed to determine the prevalence of left ventricular systolic dysfunction (LVSD), including symptomatic (ie, heart failure [HF]) and asymptomatic LVSD in adult lymphoma survivors (LSs) after autologous hematopoietic stem-cell transplantation (auto-HCT) and to identify risk factors for LVSD in this population. PATIENTS AND METHODS: All LSs treated with auto-HCT as adults in Norway from 1987 to 2008 were eligible for this national cross-sectional study. Asymptomatic LVSD was defined as left ventricular ejection fraction less than 50% by echocardiography, and HF was defined according to current recommendations. The results in LSs were compared with those found in an age- and sex-matched (1:1) control group. RESULTS: We examined 274 LSs (69% of all eligible survivors); 62% were men, the mean (± standard deviation) age was 56 ± 12 years, and mean follow-up time from lymphoma diagnosis was 13 ± 6 years. The mean cumulative doxorubicin dose was 316 ± 111 mg/m(2), and 35% of LSs had received additional radiation therapy involving the heart. We found LVSD in 15.7% of the LSs, of whom 5.1% were asymptomatic. HF patients were symptomatically mildly affected, with 8.8% of all LSs classified as New York Heart Association class II, whereas more severe HF was rare (1.8%). Compared with controls, LSs had a substantially increased LVSD risk (odds ratio, 6.6; 95% CI, 2.5 to 17.6; P < .001). A doxorubicin dose ≥ 300 mg/m(2) and cardiac radiation therapy dose greater than 30 Gy were independent risk factors for LVSD. CONCLUSION: LVSD was frequent and HF more prevalent than previously reported in LSs after auto-HCT. Our results may help to identify LSs at increased LVSD risk and can serve as a basis for targeted surveillance strategies.
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Murbræch et al. (2015) conducted a cross-sectional in Lymphoma (n=274). Autologous hematopoietic stem-cell transplantation vs. Age- and sex-matched controls was evaluated on Left ventricular systolic dysfunction (LVSD) (OR 6.6, 95% CI 2.5-17.6, p=<0.001). Lymphoma survivors treated with autologous stem-cell transplantation had a significantly higher risk of left ventricular systolic dysfunction than matched controls (OR 6.6; 95% CI 2.5-17.6; P<0.001).
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