Division of Neurosurgery, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, 36-1, Nishi-cho, Yonago, 683-8504, Tottori, Japan.
Division of Pathology, Department of Pathology, Faculty of Medicine, Tottori University, Yonago, 683- 8504, Tottori, Japan.
Sci Rep. 2024 Nov 2;14(1):26419. doi: 10.1038/s41598-024-78226-4.
In this study, we focused on calcification and diffusion restriction, which sometimes appear around the resection cavity or periventricular white matter in patients with high-grade glioma (HGG) treated with bevacizumab (BVZ), as candidate imaging biomarkers for BVZ treatment efficacy. We investigated the timing of the appearance of diffusion restriction and calcification using magnetic resonance imaging and computed tomography in 35 patients with newly diagnosed or recurrent HGG treated with BVZ. In 17 (48.6%) patients, calcification was identified around the resection cavity or periventricular white matter at a median of 12 months after the initiation of BVZ treatment. Patients with calcification had significantly longer progression-free survival (16 vs. 7 months; p = 0.0023) and overall survival (36 vs. 12 months; p = 0.0006) than those without calcification. Histopathological examination revealed the presence of scattered microcalcifications within areas of necrosis, which suggested dystrophic calcification induced by BVZ. Diffusion-restricted lesions that appeared in patients with calcification had significantly lower apparent diffusion coefficients than those in patients without calcifications, indicating the presence of treatment-related necrosis but not hypercellularity. In conclusion, the radiological finding of diffusion restriction followed by calcification could be a potential imaging biomarker for favorable clinical course in patients with HGG treated with BVZ.
在这项研究中,我们专注于在接受贝伐单抗(BVZ)治疗的高级别胶质瘤(HGG)患者中,有时在切除腔周围或脑室周围白质中出现的钙化和弥散受限,将其作为 BVZ 治疗效果的候选影像学生物标志物。我们通过磁共振成像和计算机断层扫描,对 35 名接受 BVZ 治疗的新发或复发性 HGG 患者的弥散受限和钙化出现的时间进行了研究。在 17 名(48.6%)患者中,在开始使用 BVZ 治疗后的中位 12 个月,在切除腔周围或脑室周围白质中发现了钙化。有钙化的患者无进展生存期(16 个月 vs. 7 个月;p=0.0023)和总生存期(36 个月 vs. 12 个月;p=0.0006)明显长于无钙化的患者。组织病理学检查显示坏死区域内存在散在的微钙化,这表明是 BVZ 诱导的营养不良性钙化。在有钙化的患者中出现的弥散受限病变的表观弥散系数明显低于无钙化的患者,表明存在与治疗相关的坏死,而不是细胞增多。总之,在接受 BVZ 治疗的 HGG 患者中,弥散受限继之出现钙化的影像学发现可能是一种有前景的临床病程的影像学生物标志物。