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Clinical Trials/NCT02010190
NCT02010190
Completed
Not Applicable

Vascular Assessment in Adult Survivors of Childhood Cancer

St. Jude Children's Research Hospital1 site in 1 country394 target enrollmentDecember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Risk
Sponsor
St. Jude Children's Research Hospital
Enrollment
394
Locations
1
Primary Endpoint
Mean fibrinogen
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This is an observational study that will collect data from adult survivors of childhood cancer and compare it to data collected from age- and gender-matched controls for the purpose of assessing vascular risk among cancer survivors.

Advances in cancer therapies have led to increasing numbers of adults previously treated for a pediatric malignancy, many of whom experience late adverse health-related sequelae and are at risk for developing chronic conditions related to their prior therapy. The epidemiology of many end-organ toxicities has been described, yet the pathophysiologic mechanisms of injury are incompletely understood. One mechanism may be damage to the circulatory system, in particular the endothelial layer, initiating an inflammatory state leading to dysfunction and premature atherosclerotic disease. This process may begin and significantly progress in a sub-clinical nature for many years prior to manifesting as a cardio- or cerebrovascular event. Using established and novel biomarkers predictive of atherosclerotic disease combined with unique measurements of vascular function, this study will assess pre-clinical vascular disease in a population of childhood and adolescent cancer survivors. The goals of this project are to investigate the effects of cancer therapy on the vascular system and acquire new knowledge with which to risk-stratify survivors and plan interventional studies to prevent or reduce premature vascular morbidity and mortality.

Detailed Description

PRIMARY OBJECTIVES: * Evaluate biomarkers of vascular injury (inflammation, hemostasis, endothelial activation) among childhood cancer survivors compared to age/gender-matched controls. * Assess vascular function among childhood cancer survivors compared to age/gender-matched controls. SECONDARY OBJECTIVE: * Investigate additional biomarkers of vascular health and function among childhood cancer survivors compared to age/gender-matched controls. Eligible persons who consent to participate in this trial will be asked to do the following: * Vital sign measurement including resting heart rate, blood pressure, height, and weight. * Biomarker analysis will be completed by the Cytokine Reference Laboratory, Department of Pediatrics, University of Minnesota Medical School and the Vascular Biology Center (VBC), Department of Medicine, University of Minnesota Medical School. * An echocardiogram to assess cardiac function. * Pulse wave analysis will be measured with the CR-2000 Cardiovascular Profiling System. * Pulse contour analysis will be studied using the Endo-PAT2000 system. * Pulse wave velocity will be assessed using the SphygomoCor CVP Clinical System.

Registry
clinicaltrials.gov
Start Date
December 2013
End Date
July 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Mean fibrinogen

Time Frame: Once, at first clinic visit

Mean high sensitivity C-reactive protein (hsCRP)

Time Frame: Once, at first clinic visit

Mean CEC surface expression of vascular cell adhesion molecule-1 (VCAM-1)

Time Frame: Once, at first clinic visit

Mean larger artery elasticity

Time Frame: Once, at first clinic visit

Secondary Outcomes

  • Mean von Willebrand factor (vWF)(Once, at first clinic visit)
  • Mean tissue-type plasminogen activator (tPA)(Once, at first clinic visit)
  • Mean reactive hyperemia peripheral arterial tonometry (RH-PAT) ratio(Once, at first clinic visit)
  • Mean D-dimer(Once, at first clinic visit)
  • Mean plasminogen activator inhibitor-1 (PAI-1)(Once, at first clinic visit)
  • Mean small artery elasticity (SAE)(Once, at first clinic visit)
  • Mean number of circulating endothelial cells (CECs)(Once, at first clinic visit)
  • Mean carotid-femoral pulse wave velocity(Once, at first clinic visit)
  • Mean CEC surface expression of P-selectin(Once, at first clinic visit)
  • Mean soluble vascular cell adhesion molecule-1 (VCAM-1)(Once, at first clinic visit)
  • Mean lipoprotein(a)(Once, at first clinic visit)
  • Mean soluble P-selectin(Once, at first clinic visit)

Study Sites (1)

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