光谱磁共振成像在新诊断胶质母细胞瘤的立体定向活检和放疗指导中的实用性

IF 2.2 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Tomography Pub Date : 2024-03-20 DOI:10.3390/tomography10030033
Abinand C. Rejimon, Karthik K Ramesh, Anuradha G. Trivedi, Vicki Huang, E. Schreibmann, B. Weinberg, Lawrence R. Kleinberg, Hui-Kuo G. Shu, Hyunsuk Shim, Jeffrey J. Olson
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引用次数: 0

摘要

目前胶质瘤的诊断和治疗方法存在局限性,影响了患者的生存。我们建议将光谱磁共振成像作为标准磁共振成像的辅助手段,以弥补这些不足。光谱磁共振成像是一种容积磁共振成像技术,能够根据胆碱(Cho)的升高和N-乙酰天冬氨酸(NAA)的降低来识别肿瘤浸润。我们介绍了光谱成像的临床可转化性,Cho/NAA ≥ 5x 的阈值可用于在一名确诊为非增强型胶质瘤的患者身上划定活检目标。然后,我们描述了代谢物成像检测到的治疗不足的肿瘤与新诊断的贝利诺斯他和化疗治疗的 GBM 患者的试点研究的总生存率(OS)之间的关系。根据放疗前Cho/NAA≥2倍与治疗后T1加权对比增强(T1w-CE)体积之差的中位数,将每个队列(对照组和贝利诺司特)分成亚组。我们使用 Kaplan-Meier 估计器计算每个亚组的中位 OS。当Cho/NAA≥2x与T1w-CE体积的差异高于中位数时,中位OS为14.4个月,而当这一差异低于中位数时,中位OS为34.3个月。两个亚组的 T1w-CE 容量相似。我们发现,通过光谱检测到的未治疗肿瘤体积较小的患者的生存预后较好。
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The Utility of Spectroscopic MRI in Stereotactic Biopsy and Radiotherapy Guidance in Newly Diagnosed Glioblastoma
Current diagnostic and therapeutic approaches for gliomas have limitations hindering survival outcomes. We propose spectroscopic magnetic resonance imaging as an adjunct to standard MRI to bridge these gaps. Spectroscopic MRI is a volumetric MRI technique capable of identifying tumor infiltration based on its elevated choline (Cho) and decreased N-acetylaspartate (NAA). We present the clinical translatability of spectroscopic imaging with a Cho/NAA ≥ 5x threshold for delineating a biopsy target in a patient diagnosed with non-enhancing glioma. Then, we describe the relationship between the undertreated tumor detected with metabolite imaging and overall survival (OS) from a pilot study of newly diagnosed GBM patients treated with belinostat and chemoradiation. Each cohort (control and belinostat) were split into subgroups using the median difference between pre-radiotherapy Cho/NAA ≥ 2x and the treated T1-weighted contrast-enhanced (T1w-CE) volume. We used the Kaplan–Meier estimator to calculate median OS for each subgroup. The median OS was 14.4 months when the difference between Cho/NAA ≥ 2x and T1w-CE volumes was higher than the median compared with 34.3 months when this difference was lower than the median. The T1w-CE volumes were similar in both subgroups. We find that patients who had lower volumes of undertreated tumors detected via spectroscopy had better survival outcomes.
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来源期刊
Tomography
Tomography Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
2.70
自引率
10.50%
发文量
222
期刊介绍: TomographyTM publishes basic (technical and pre-clinical) and clinical scientific articles which involve the advancement of imaging technologies. Tomography encompasses studies that use single or multiple imaging modalities including for example CT, US, PET, SPECT, MR and hyperpolarization technologies, as well as optical modalities (i.e. bioluminescence, photoacoustic, endomicroscopy, fiber optic imaging and optical computed tomography) in basic sciences, engineering, preclinical and clinical medicine. Tomography also welcomes studies involving exploration and refinement of contrast mechanisms and image-derived metrics within and across modalities toward the development of novel imaging probes for image-based feedback and intervention. The use of imaging in biology and medicine provides unparalleled opportunities to noninvasively interrogate tissues to obtain real-time dynamic and quantitative information required for diagnosis and response to interventions and to follow evolving pathological conditions. As multi-modal studies and the complexities of imaging technologies themselves are ever increasing to provide advanced information to scientists and clinicians. Tomography provides a unique publication venue allowing investigators the opportunity to more precisely communicate integrated findings related to the diverse and heterogeneous features associated with underlying anatomical, physiological, functional, metabolic and molecular genetic activities of normal and diseased tissue. Thus Tomography publishes peer-reviewed articles which involve the broad use of imaging of any tissue and disease type including both preclinical and clinical investigations. In addition, hardware/software along with chemical and molecular probe advances are welcome as they are deemed to significantly contribute towards the long-term goal of improving the overall impact of imaging on scientific and clinical discovery.
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