Incidence and outcomes of cancer treatment-related cardiomyopathy among referrals for advanced heart failure

被引:7
作者
Araujo-Gutierrez R. [1 ]
Ibarra-Cortez S.H. [2 ]
Estep J.D. [3 ]
Bhimaraj A. [3 ]
Guha A. [3 ]
Hussain I. [3 ]
Park M.H. [3 ]
Torre-Amione G. [3 ]
Trachtenberg B.H. [3 ]
机构
[1] Department of Heart Failure & Transplant Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston Methodist Research Institute, 6565 Fannin St, F657, Houston, 77030, TX
[2] Department of Structural Heart Disease, Houston Methodist DeBakey Heart & Vascular Center, Houston Methodist Research Institute, 6565 Fannin St. F766, Houston, 77030, TX
[3] Department of Heart Failure & Transplant Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston Methodist Hospital, 6550 Fannin St. Suite 1901, Houston, 77030, TX
关键词
Anthracyclines; Cancer–related cardiomyopathy; Chemotherapy-induced cardiomyopathy; Heart failure; Heart transplant; Heart transplantation; Left ventricular assist device; Mechanical circulatory support; Radiation-induced cardiomyopathy;
D O I
10.1186/s40959-018-0029-y
中图分类号
学科分类号
摘要
Background: Approximately 2–3% of patients undergoing advanced heart failure therapies such as left ventricular assist devices (LVAD) and orthotropic heart transplantation (OHT) have chemotherapy-related cardiomyopathy, according to analyses of large databases such as United Network for Organ Sharing (UNOS) or Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) registries. While these studies have shown similar survival outcomes post-interventions, these databases by definition exclude patients referred for advanced therapies but do not receive them, and thus there is little data on overall outcomes of such patients. Given the lack of nuance in the diagnoses in large registries and the possibility that many cancer treatment-related cardiomyopathy (CCMP) patients might be misclassified by the generic “non-ischemic” or “dilated” cardiomyopathies, we investigated the incidence and clinical outcomes of CCMP patients among advanced heart failure (HF) referrals at a single high volume institution. Methods: All referrals from 2013 to 2016 were evaluated for type of cardiomyopathy, with careful chart review. Outcomes such as LVAD, OHT and death were compared between CCMP and other cardiomyopathies. Results: Of 553 referrals for advanced HF, 19 (3.4%) were for CCMP. There was a higher percentage of patients receiving advanced therapies in the CCMP vs. non-ischemic cardiomyopathy (NICMP) and ischemic cardiomyopathy (ICMP) (42.1% vs 30.2% vs 33.6%, not significant). Of the CCMP patients, 3 had OHT directly, 2 had LVAD followed by OHT, and 3 had LVADs as bridge to candidacy or destination therapy. Fifty-eight percent of the CCMP did not receive LVAD or OHT compared to 69.8% and 66.3 of the NICMP and ICMP, respectively (p = 0.0388). Independent of type of advanced therapy, survival was significantly higher in the CCMP group compared to NICMP and ICMP (93.3% vs 84.8% vs 73.8%, respectively P = 0.0021 for 1 year, 93.3% vs 76.2% vs 58.3%, respectively, P = < 0.0001 for 3 year). Conclusions: In a single institution, CCMP accounts for more than 3% of all referrals for advanced HF therapies and almost 8% of NICMP. Contrary to concerns for previous cancer and sequelae of cancer treatment excluding patients for advanced therapies, a higher percentage of CCMP underwent advanced HF therapies and with similar outcomes. This is the first study to show that among patients referred for advanced therapies, CCMP patients do not have inferior outcomes compared to other cardiomyopathies regardless of the selected management strategy. © 2018, The Author(s).
引用
收藏
相关论文
共 12 条
  • [1] DeSantis C.E., Et al., Cancer treatment and survivorship statistics, 2014, CA Cancer J Clin, 64, 4, pp. 252-271, (2014)
  • [2] Kero A.E., Et al., Cardiovascular morbidity in long-term survivors of early-onset cancer: a population-based study, Int J Cancer, 134, 3, pp. 664-673, (2014)
  • [3] Oliveira G.H., Et al., Increased need for right ventricular support in patients with chemotherapy-induced cardiomyopathy undergoing mechanical circulatory support: outcomes from the INTERMACS registry (interagency registry for mechanically assisted circulatory support), J Am Coll Cardiol, 63, 3, pp. 240-248, (2014)
  • [4] Yeh E.T., Bickford C.L., Cardiovascular complications of cancer therapy: incidence, pathogenesis, diagnosis, and management, J Am Coll Cardiol, 53, 24, pp. 2231-2247, (2009)
  • [5] Pein F., Et al., Cardiac abnormalities 15 years and more after adriamycin therapy in 229 childhood survivors of a solid tumour at the Institut Gustave Roussy, Br J Cancer, 91, 1, pp. 37-44, (2004)
  • [6] Andersson A., Et al., Long-term risk of cardiovascular disease in Hodgkin lymphoma survivors--retrospective cohort analyses and a concept for prospective intervention, Int J Cancer, 124, 8, pp. 1914-1917, (2009)
  • [7] Hooning M.J., Et al., Long-term risk of cardiovascular disease in 10-year survivors of breast cancer, J Natl Cancer Inst, 99, 5, pp. 365-375, (2007)
  • [8] Oliveira G.H., Et al., Advanced heart failure therapies for patients with chemotherapy-induced cardiomyopathy, Circ Heart Fail, 7, 6, pp. 1050-1058, (2014)
  • [9] Oliveira G.H., Et al., Characteristics and survival of patients with chemotherapy-induced cardiomyopathy undergoing heart transplantation, J Heart Lung Transplant, 31, 8, pp. 805-810, (2012)
  • [10] Lenneman A.J., Et al., Heart transplant survival outcomes for adriamycin-dilated cardiomyopathy, Am J Cardiol, 111, 4, pp. 609-612, (2013)