We read with interest the report by Cloughesy et al on the activity of cabozantinib in recurrent glioblastoma (GBM) patients with prior anti-angiogenic therapy.1 In their subset analysis, they reported overall survival (OS) results using 2 different cabozantinib doses: 4.1 months (95% CI: 1.4–16.7) in the 140 mg group (n = 12); 4.6 (95% CI: 2.9–5.6) in the 100 mg group (n = 58); OS for combined groups was 4.6 months. Of the 70 patients in the analysis, 57 (81%) with prior anti-angiogenic therapy had bevacizumab (BEV). In their discussion, the authors raise the issue of "how best to define a meaningful response (eg, objective response rate, progression-free survival)."1 We argue, because of the vagaries in interpreting MRIs in patients receiving BEV or other anti-angiogenic agents, the most meaningful endpoint is OS. Relative to this, we suggest literature can provide a valuable benchmark, as the OS outcome for these patients tends to be relatively uniform. Such a review of the literature2 exemplifies this argument and compares well with the reported results in the cabozantinib study (ie, group 3 below):
Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00306932607174,00302841026182,alsfakia@gmail.com
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