4.6 Article

Bevacizumab Combined with Corticosteroids Does Not Improve the Clinical Outcome of Nasopharyngeal Carcinoma Patients With Radiation-Induced Brain Necrosis

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FRONTIERS IN ONCOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.746941

关键词

radiation-induced brain necrosis; bevacizumab combined with corticosteroid; real-world data; nasopharyngeal carcinoma; bevacizumab monotherapy

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资金

  1. National Science Fund for Distinguished Young Scholars [81925031]
  2. Projects of International Cooperation and Exchanges NSFC [81820108026]
  3. Science and Technology Program of Guangzhou [202007030001]
  4. National Natural Science Foundation of China [82003389, 81872549]
  5. Young Teacher Training Program of Sun Yat-sen University [20ykpy106]
  6. Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence Fund [2019012]
  7. National Medical Research Council Singapore Clinician Scientist Award [NMRC/CSA-INV/0027/2018]
  8. National Research Foundation Proton Competitive Research Program [NRF-CRP17-2017-05]
  9. Ministry of Education Tier 3 Academic Research Fund [MOE2016-T3-1-004]
  10. Duke-NUS Oncology Academic Program Goh Foundation Proton Research Programme
  11. NCCS Cancer Fund
  12. Kua Hong Pak Head and Neck Cancer Research Programme

向作者/读者索取更多资源

The study compared the clinical outcomes of patients with radiation-induced brain necrosis who were treated with bevacizumab combined with corticosteroids and those with bevacizumab monotherapy, showing that the combination therapy did not lead to better clinical outcomes and did not reduce recurrence rates. The most common adverse events of bevacizumab were hypertension, nosebleed, and fatigue, with no significant difference in severe adverse events between the two groups.
Objective Our aim was to compare the clinical outcomes of patients treated with bevacizumab combined with corticosteroids and those with bevacizumab monotherapy from a radiation-induced brain necrosis (RN) registry cohort (NCT03908502). Methods We utilized clinical data from a prospective RN registry cohort (NCT03908502) from July 2017 to June 2020. Patients were considered eligible if they had symptomatic RN after radiotherapy for nasopharyngeal carcinoma (NPC) and received bevacizumab (5 mg/kg, two to four cycles) with a minimum follow-up time of 3 months. The primary outcome was a 2-month response rate determined by MRI and clinical symptoms. Secondary outcomes included quality of life [evaluated by the abbreviated World Health Organization Quality of Life (WHOQOL-BREF) questionnaire] and cognitive function (evaluated by the Montreal Cognitive Assessment scale) at 2 months, RN recurrence during follow-up, and adverse events. Results A total of 123 patients (34 in the combined therapy group and 89 in the monotherapy group) were enrolled in our study with a median follow-up time of 0.97 year [interquartile range (IQR) = 0.35-2.60 years]. The clinical efficacy of RN did not differ significantly between patients in these two groups [odds ratio (OR) = 1.642, 95%CI = 0.584-4.614, p = 0.347]. Furthermore, bevacizumab combined with corticosteroids did not reduce recurrence compared with bevacizumab monotherapy [hazard ratio (HR) = 1.329, 95%CI = 0.849-2.079, p = 0.213]. The most common adverse events of bevacizumab were hypertension (17.89%), followed by nosebleed (8.13%) and fatigue (8.13%). There was no difference in grade 2 or more severe adverse events between the two groups (p = 0.811). Interpretation Our results showed that the treatment strategy of combining bevacizumab with corticosteroids did not lead to better clinical outcomes for RN patients with a background of radiotherapy for nasopharyngeal carcinoma.

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