
pmid: 38219019
pmc: PMC11066942
Abstract Background Radiological progression may originate from progressive disease (PD) or pseudoprogression/treatment-associated changes. We assessed radiological progression in O6-methylguanine-DNA methyltransferase (MGMT) promoter-methylated glioblastoma treated with standard-of-care chemoradiotherapy with or without the integrin inhibitor cilengitide according to the modified response assessment in neuro-oncology (RANO) criteria of 2017. Methods Patients with ≥ 3 follow-up MRIs were included. Preliminary PD was defined as a ≥ 25% increase of the sum of products of perpendicular diameters (SPD) of a new or increasing lesion compared to baseline. PD required a second ≥25% increase of the SPD. Treatment-associated changes require stable or regressing disease after preliminary PD. Results Of the 424 evaluable patients, 221 patients (52%) were randomized into the cilengitide and 203 patients (48%) into the control arm. After chemoradiation with or without cilengitide, preliminary PD occurred in 274 patients (65%) during available follow-up, and 88 of these patients (32%) had treatment-associated changes, whereas 67 patients (25%) had PD. The remaining 119 patients (43%) had no further follow-up after preliminary PD. Treatment-associated changes were more common in the cilengitide arm than in the standard-of-care arm (24% vs. 17%; relative risk, 1.3; 95% CI, 1.004–1.795; P = .047). Treatment-associated changes occurred mainly during the first 6 months after RT (54% after 3 months vs. 13% after 6 months). Conclusions With the modified RANO criteria, the rate of treatment-associated changes was low compared to previous studies in MGMT promoter-methylated glioblastoma. This rate was higher after cilengitide compared to standard-of-care treatment. Confirmatory scans, as recommended in the modified RANO criteria, were not always available reflecting current clinical practice.
Male, Adult, Cancer Research, 610, 610 Medicine & health, Tumor Suppressor Proteins/genetics, Chemoradiotherapy/methods, SDG 3 - Good Health and Well-being, Journal Article, Humans, Promoter Regions, Genetic, DNA Modification Methylases, Clinical Neuro-Oncology, info:eu-repo/classification/ddc/610, Aged, Brain Neoplasms/genetics, Aged, 80 and over, Brain Neoplasms, Research Support, Non-U.S. Gov't, Tumor Suppressor Proteins, Chemoradiotherapy, Middle Aged, DNA Methylation, DNA Repair Enzymes/genetics, Prognosis, Magnetic Resonance Imaging, Glioblastoma/genetics, 10040 Clinic for Neurology, DNA Repair Enzymes, Oncology, Randomized Controlled Trial, Disease Progression, Female, Neurology (clinical), DNA Modification Methylases/genetics, Glioblastoma, Snake Venoms, Follow-Up Studies
Male, Adult, Cancer Research, 610, 610 Medicine & health, Tumor Suppressor Proteins/genetics, Chemoradiotherapy/methods, SDG 3 - Good Health and Well-being, Journal Article, Humans, Promoter Regions, Genetic, DNA Modification Methylases, Clinical Neuro-Oncology, info:eu-repo/classification/ddc/610, Aged, Brain Neoplasms/genetics, Aged, 80 and over, Brain Neoplasms, Research Support, Non-U.S. Gov't, Tumor Suppressor Proteins, Chemoradiotherapy, Middle Aged, DNA Methylation, DNA Repair Enzymes/genetics, Prognosis, Magnetic Resonance Imaging, Glioblastoma/genetics, 10040 Clinic for Neurology, DNA Repair Enzymes, Oncology, Randomized Controlled Trial, Disease Progression, Female, Neurology (clinical), DNA Modification Methylases/genetics, Glioblastoma, Snake Venoms, Follow-Up Studies
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