Cornell Isabel, Al Busaidi Ayisha, Wastling Stephen, Anjari Mustafa, Cwynarski Kate, Fox Christopher P, Martinez-Calle Nicolas, Poynton Edward, Maynard John, Thust Steffi C
UCL Institute of Neurology, Department of Brain Rehabilitation and Repair, Queen Square, London WC1N 3BG, UK.
Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, London WC1N 3BG, UK.
J Pers Med. 2023 Jul 24;13(7):1182. doi: 10.3390/jpm13071182.
Primary Central Nervous System Lymphoma (PCNSL) is a highly malignant brain tumour. We investigated dynamic changes in tumour volume and apparent diffusion coefficient (ADC) measurements for predicting outcome following treatment with MATRix chemotherapy in PCNSL. Patients treated with MATRix ( = 38) underwent T1 contrast-enhanced (T1CE) and diffusion-weighted imaging (DWI) before treatment, after two cycles and after four cycles of chemotherapy. Response was assessed using the International PCNSL Collaborative Group (IPCG) imaging criteria. ADC histogram parameters and T1CE tumour volumes were compared among response groups, using one-way ANOVA testing. Logistic regression was performed to examine those imaging parameters predictive of response. Response after two cycles of chemotherapy differed from response after four cycles; of the six patients with progressive disease (PD) after four cycles of treatment, two (33%) had demonstrated a partial response (PR) or complete response (CR) after two cycles. ADC at baseline, T1CE at baseline and T1CE percentage volume change differed between response groups (0.005 < < 0.038) and were predictive of MATRix treatment response (area under the curve: 0.672-0.854). Baseline ADC and T1CE metrics are potential biomarkers for risk stratification of PCNSL patients early during remission induction therapy with MATRix. Standard interim response assessment (after two cycles) according to IPCG imaging criteria does not reliably predict early disease progression in the context of a conventional treatment approach.
原发性中枢神经系统淋巴瘤(PCNSL)是一种高度恶性的脑肿瘤。我们研究了肿瘤体积和表观扩散系数(ADC)测量值的动态变化,以预测PCNSL患者接受MATRix化疗后的治疗结果。接受MATRix治疗的患者(n = 38)在治疗前、化疗两个周期后和四个周期后接受了T1加权增强(T1CE)和扩散加权成像(DWI)检查。使用国际PCNSL协作组(IPCG)成像标准评估疗效。使用单因素方差分析在不同反应组之间比较ADC直方图参数和T1CE肿瘤体积。进行逻辑回归分析以检验那些预测反应的成像参数。化疗两个周期后的反应与四个周期后的反应不同;在四个周期治疗后出现疾病进展(PD)的6例患者中,有2例(33%)在两个周期后显示部分缓解(PR)或完全缓解(CR)。不同反应组之间基线时的ADC、基线时的T1CE和T1CE体积变化百分比存在差异(0.005 < P < 0.038),并且可预测MATRix治疗反应(曲线下面积:0.672 - 0.854)。基线ADC和T1CE指标是PCNSL患者在接受MATRix缓解诱导治疗早期进行风险分层的潜在生物标志物。根据IPCG成像标准进行的标准中期反应评估(两个周期后)在传统治疗方法背景下不能可靠地预测早期疾病进展。