4.7 Article

Early treatment response evaluation using FET PET compared to MRI in glioblastoma patients at first progression treated with bevacizumab plus lomustine

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SPRINGER
DOI: 10.1007/s00259-018-4082-4

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CCNU; Amino acid PET; Glioma; Treatment-related changes; Tumour relapse

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  1. Wilhelm-Sander Stiftung, Germany [2016.069.1]

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BackgroundThe goal of this prospective study was to compare the value of both conventional MRI and O-(2-F-18-fluoroethyl)-L-tyrosine (FET) PET for response evaluation in glioblastoma patients treated with bevacizumab plus lomustine (BEV/LOM) at first progression.MethodsAfter chemoradiation with concomitant and adjuvant temozolomide, 21 IDH wild-type glioblastoma patients at first progression (age range, 33-75years; MGMT promoter unmethylated, 81%) were treated with BEV/LOM. Contrast-enhanced MRI and FET-PET scans were performed at baseline and after 8-10weeks. We obtained FET metabolic tumor volumes (MTV) and tumor/brain ratios. Threshold values of FET-PET parameters for treatment response were established by ROC analyses using the post-progression overall survival (OS) />9months as the reference. MRI response assessment was based on RANO criteria. The predictive ability of FET-PET thresholds and MRI changes on early response assessment was evaluated subsequently concerning OS using uni- and multivariate survival estimates.ResultsEarly treatment response as assessed by RANO criteria was not predictive for an OS>9months (P=0.203), whereas relative reductions of all FET-PET parameters significantly predicted an OS>9months (P<0.05). The absolute MTV at follow-up enabled the most significant OS prediction (sensitivity, 85%; specificity, 88%; P=0.001). Patients with an absolute MTV below 5ml at follow-up survived significantly longer (12 vs. 6months, P<0.001), whereas early responders defined by RANO criteria lived only insignificantly longer (9 vs. 6months; P=0.072). The absolute MTV at follow-up remained significant in the multivariate survival analysis (P=0.006).ConclusionsFET-PET appears to be useful for identifying responders to BEV/LOM early after treatment initiation.

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