Progression of cognitive dysfunction in NPC survivors with radiation-induced brain necrosis: A prospective cohort

Radiother Oncol. 2024 Jan:190:110033. doi: 10.1016/j.radonc.2023.110033. Epub 2023 Nov 27.

Abstract

Background and purpose: The evidence of longitudinal changes in cognition in nasopharyngeal carcinoma (NPC) survivors with radiation-induced brain necrosis (RIBN) after radiotherapy (RT) remained insufficient. We aimed to estimate the clinical progression rate of cognitive decline and identify patients with differential decline rates.

Materials and methods: Based on an ongoing prospective cohort study, NPC patients aged ≥18 years old and diagnosed with RIBN were included in this current analysis if they finished the time frame of 3-year follow-up and had at least twice cognition assessments. The Chinese version of the Montreal Cognitive Assessment (MoCA) was used to assess the cognitive state. Linear mixed-effect models were used to analyze the annual progression rates of MoCA total and seven sub-items scores.

Results: Among 134 patients in this study, the transition probability from normal to mild/moderate cognitive dysfunction were 14.2 % (19/134) and 1.49 % (2/134) respectively during the median follow-up time of 2.35 years. The total MoCA score declined by -0.569 (SE 0.208) points annually (p = 0.008). Patients with ≤6 years of duration from RT to RIBN have higher annual progression rate of total scores [-0.851 (SE 0.321), p = 0.013; p for interaction = 0.041].

Conclusion: Our findings of the annual decline rate of cognition in NPC patients with RIBN from a 3-year longitudinal data, particularly for those who developed RIBN rapidly after RT, have important implications for the upcoming clinical trials designed to prevent or decrease cognitive decline in NPC patients with RIBN, regarding the selection of study patients and the calculation of sample size.

Keywords: Brain necrosis; Cognitive dysfunction; Linear mixed-effect model; Nasopharyngeal carcinoma; Radiotherapy.

MeSH terms

  • Adolescent
  • Adult
  • Brain / pathology
  • Cognitive Dysfunction* / etiology
  • Humans
  • Nasopharyngeal Carcinoma / pathology
  • Nasopharyngeal Carcinoma / radiotherapy
  • Nasopharyngeal Neoplasms* / radiotherapy
  • Necrosis / pathology
  • Prospective Studies
  • Survivors