Journal of Clinical Neuroscience | 2019

Tumour volume reduction following PET guided intensity modulated radiation therapy and temozolomide in IDH mutated anaplastic glioma

 
 
 
 
 

Abstract


The role of maximal surgical debulking in isocitrate dehydrogenase (IDH) mutated anaplastic glioma prior to adjuvant radiation therapy remains uncertain. This study assessed the reduction in tumour volume following intensity modulated radiation therapy (IMRT) and temozolomide in this favourable and more responsive tumour pathology. 56 patients were managed from 2011 to 2014 and 53 had residual disease. To assess radiological response, tumour volumes were created on representative T1/T2Flair MRI sequences using identical slice-levels in three planes for pre-IMRT, month\u202f+\u202f3 and month\u202f+\u202f12 post-IMRT scans. Change in volumes was assessed between time periods. Progression-free survival (PFS) was calculated from start of radiotherapy. Median follow-up for survivors is 48.2\u202fmonths. Pathology was anaplastic oligodendroglioma (AOD) and anaplastic astrocytoma IDH-mutated (AAmut) in 32 and 21 patients respectively. 93% received sequential chemotherapy. The median residual disease on T1 and T2Flair imaging was 9.7\u202fcm3 and 20.6\u202fcm3. 17 patients relapsed for projected 5\u202fyear PFS of 74.9%; with 8 isolated relapses within initial surgical site. On MRI at month\u202f+\u202f3, the median volume for T1 and T2Flair reduced by 69.4% and 67.3% respectively; which further decreased to 82.4% and 81.3% at month\u202f+\u202f12. By month\u202f+\u202f12, 69.2% and 62.2% of patients had >75% volume reduction. Patients with AOD had superior reduction at month\u202f+\u202f3 compared with AAmut (p\u202f=\u202f0.02); but equivalent reduction at month\u202f+\u202f12 (p\u202f=\u202f0.14). Thus, in patients with anaplastic glioma harbouring an IDH mutation, where an attempt at near-total resection may be associated with unacceptable morbidity, this data suggests that the radiation therapy may provide effective cytoreduction of residual disease.

Volume 59
Pages 68-74
DOI 10.1016/j.jocn.2018.11.005
Language English
Journal Journal of Clinical Neuroscience

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