Cardiac structural and functional alterations in cancer cachexia

• Author / Creator

  Kazemi Bajestani, Seyyed Mohammad Reza

• Background: Cancer cachexia is referred to as a wasting condition, with skeletal muscle and fat loss. Although heart atrophy is recognized as a notable component of experimental cancer cachexia models, it has not been characterized in human studies. The contribution of cardiac structural and functional impairment to worsening performance status, fatigue progression and dyspnea, is known in the context of heart failure; however, the pertinent clinical information in cancer cachexia has never been examined. Cancer cachexia still does not have an approved therapy; regulatory agencies claim functional measures such as stair climbing test improvement as a clinical benefit of experimental agents, however, the matter of heart function and structure at baseline and its alteration over time (as a potential source of functional variation) is ignored. In the absence of any clinical evidence for cardiac structure or function changes in cachexia context, two retrospective evaluations of cardiac function were conducted in pursuit of preliminary evidence of either: a) altered cardiac function over time in renal cell carcinoma patients or, b) evidence of concurrent cachexia and abnormally low cardiac mass in cirrhosis patients with or without hepatocellular carcinoma. My major hypothesis through a longitudinal work was that heart is being atrophied and is dysfunctional in parallel to cancer cachexia progression. Methods: Three different clinical projects were considered for my PhD research (two retrospective/chart reviews and one longitudinal cohort study). In all these studies, standard of care computed tomography cross-sectional images were utilized to quantify skeletal muscle and fat. In the longitudinal study, we measured heart systolic [left ventricular ejection fraction (LVEF) and global longitudinal strain] and diastolic function in addition to left ventricular mass at baseline (before start of carboplatin-based therapy) and over time (4 months later) in patients with metastatic non-small cell lung cancer (n=72). Standard questionnaires for assessment of performance status, fatigue and dyspnea also were applied. For the first retrospective study, cirrhotic patients (n=100) with or without hepatocellular carcinoma were studied; values for left ventricular mass were abstracted from available echocardiography reports before liver transplant. For the second retrospective study in renal cell carcinoma patients (n=47), several multigated acquisition scans were gathered over one year of assessment to detect changes in LVEF. Results: For the first time we demonstrated the occurrence of left ventricular mass atrophy in a group of patients with progressive cachexia and non-small cell lung cancer. Atrophy of left ventricular mass (median overall -8.9%, p8.9% of left ventricular mass associated with loss of skeletal muscle (OR, 95% CI) [4.5 (1.4-14.8) p1 SD below sex-specific mean value of left ventricular mass indexed by height2) compared to the patients with average left ventricular mass index, sarcopenia was more prevalent (70.6% vs. 27.3%; 6.4 (1.9–20.7); p = 0.002). Fat loss also showed a trend to be more prevalent in group of patients with low left ventricular mass index. In renal cell carcinoma patients multigated acquisition scan-defined cardio-toxicity appeared in 8/47 (17%) patients. This targeted therapy-induced cardio-toxicity was related to high fat mass at baseline [9.5 (1.1-86.0), p=0.04]; also the percentage of skeletal muscle loss over 1 year in patients with cardio-toxicity was greater than patients without cardiotoxicity [median loss -7.0% versus 0%, respectively; p=0.04]. Conclusion: Dynamic cardiac atrophy is reported for the first time in human patients with progressive cancer cachexia. Cardiac status in terms of structure and function should be recognized in further clinical trials.

• Subjects / Keywords

  • cardiac function
  • cardio-toxicity
  • skeletal muscle loss
  • fat loss
  • cardiac atrophy
  • cancer cachexia

• Graduation date

  Fall 2017

• Type of Item

  Thesis

• Degree

  Doctor of Philosophy

• DOI

  https://doi.org/10.7939/R3KD1R233

• License

  This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.