Abstract

Simple SummaryRadiotherapy has become a common treatment modality for nasopharyngeal carcinoma, and concurrent chemoradiation therapy prolongs the survival of patients. Radiotherapy leads to the increased generation of reactive oxygen species and free radicals to destroy abnormal cell growths within normal cell environmental conditions. However, the late effects on “bystander” organs (e.g., extracranial arteries) among survivors after radiotherapy have become increasingly prevalent. This study showed radiation-related extracranial vasculopathy is a progressive process that begins immediately after radiotherapy with significantly increased carotid IMT compared to the control group during the 9-year follow-up. Chronic inflammation and oxidative stress might serve to drive the process and also contribute to increased platelet activation.Radiation-related extracranial vasculopathy is a common late effect after radiation in patients with nasopharyngeal carcinoma (NPC). We proposed the hypothesis that radiation-related extracranial vasculopathy is a progressive process that can begin immediately after radiotherapy and persist for a longer period, and inflammation and oxidative stress may play a pivotal role in this process. Thirty-six newly diagnosed NPC patients were assessed with B-mode ultrasound for the common carotid artery (CCA) intima media thickness (IMT) measurement as well as surrogate markers at three different stages (baseline, immediately after concurrent chemoradiation therapy (CCRT), and 9 years after enrollment). A healthy control group was also recruited for comparison. Surrogate markers including a lipid profile, HbA1c, inflammation, oxidative stress, and platelet activation markers were assessed. The mean CCA IMT in the NPC group were increased immediately after CCRT (p = 0.043). The mean CCA IMT value after a 9-year follow-up also showed a significant increase in NPC and control group, respectively (p < 0.0001 and p < 0.0001, paired t test). The annual increase mean CCA IMT (mm) was 0.053 ± 0.025 and 0.014 ± 0.013 in NPC and control group, respectively (p < 0.0001). The baseline high sensitivity CRP (hs-CRP), thiol, TBARS, and CD63 level were significantly higher in the NPC group (hs-CRP, p = 0.001, thiol, p < 0.0001, TBARS, p = 0.05, and CD63 level, p = 0.04). The thiol and TBARS levels were significantly lower in NPC patients immediately after CCRT (thiol, p < 0.0001, and TBARS, p = 0.043). The CD62P level was significantly higher while the thiol level was significantly lower in the NPC group after a 9-year follow-up (CD62P level, p = 0.007; and thiol level, p = 0.004). Radiation-related extracranial vasculopathy is a progressive process that begins immediately after radiotherapy with significantly increased carotid IMT compared to the control group during the 9-year follow-up. Chronic inflammation and oxidative stress might serve to drive the process and also contribute to increased platelet activation.

Highlights

  • Nasopharyngeal carcinoma (NPC) is characterized by its unique geographic distribution in southeastern China and Taiwan, and both environmental factors and genetic traits contribute to its development [1]

  • There is accumulating evidence indicating that inflammation and oxidative stress may play a pivotal role in the process of radiation-related extracranial vasculopathy [8,9]

  • The mean diastolic blood pressure during extra-cranial color-coded duplex sonography (ECCS) examination was higher in the nasopharyngeal carcinoma (NPC) group (p = 0.001)

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Summary

Introduction

Nasopharyngeal carcinoma (NPC) is characterized by its unique geographic distribution in southeastern China and Taiwan, and both environmental factors and genetic traits contribute to its development [1]. With the increased number of five-year cancer survivors, survivorship has become an important issue [3,4]. A recent Taiwan National Health Insurance Research Database study demonstrated that NPC survivors had higher stroke risks but the age of onset of stroke was 10 years earlier than that for the general population [3]. Radiation therapy leads to the increased generation of reactive oxygen species (ROS) and free radicals to destroy abnormal cell growths within normal cell environmental conditions. When cellular repair and free radical scavenger systems cannot counteract these insults, oxidative damage occurs and has the consequence of abnormal cellular structure and function [3]. There is accumulating evidence indicating that inflammation and oxidative stress may play a pivotal role in the process of radiation-related extracranial vasculopathy [8,9]

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