血清乳酸脱氢酶作为接受stupp方案治疗的IDH野生型胶质母细胞瘤患者治疗反应的预后指标。

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY
Paolo Tini, Elisa Cinelli, Mariya Yavorska, Flavio Donnini, Francesco Marampon, Pierpaolo Pastina, Giovanni Rubino, Salvatore Chibbaro, Alfonso Cerase, Maria Antonietta Mazzei, Anna Maria Di Giacomo, Giuseppe Minniti
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Clinical data, including hematologic parameters (e.g., LDH), imaging (MRI), and MGMT promoter methylation status, were collected. All patients received RT and TMZ following the Stupp protocol. Serum LDH levels were measured one week before RT, and Radiological Response (RR) was assessed using RANO criteria. Overall survival (OS), progression-free survival (PFS), and RR were primary endpoints. Statistical analyses included Kaplan-Meier, Cox regression, and decision tree analysis for LDH cut-off determination.</p><p><strong>Results: </strong>In a cohort of 147 IDH wild-type glioblastoma patients treated with the Stupp protocol, the median OS was 14 months and median PFS was 8 months. Elevated baseline LDH levels were associated with significantly poorer outcomes, showing a median OS of 9 months versus 20 months and a median PFS of 6 months versus 13 months for lower LDH levels (p < 0.001 and p = 0.0001, respectively). 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引用次数: 0

摘要

背景和目的:乳酸脱氢酶(LDH)升高是肿瘤侵袭性和代谢改变的标志物,可预测各种肿瘤的治疗反应和总生存期。本研究调查了接受放疗(RT)和替莫唑胺(TMZ)治疗的胶质母细胞瘤患者血清 LDH 水平与临床结果之间的相关性:这项回顾性研究分析了2018年至2023年在Azienda Ospedaliero-Universitaria Senese放疗科接受治疗的IDH野生型胶质母细胞瘤(IDH-wt GB)患者。收集的临床数据包括血液学参数(如 LDH)、影像学(MRI)和 MGMT 启动子甲基化状态。所有患者均按照Stupp方案接受RT和TMZ治疗。RT 前一周测量血清 LDH 水平,并采用 RANO 标准评估放射学反应(RR)。总生存期(OS)、无进展生存期(PFS)和RR是主要终点。统计分析包括 Kaplan-Meier、Cox 回归和确定 LDH 临界值的决策树分析:结果:在采用Stupp方案治疗的147名IDH野生型胶质母细胞瘤患者中,中位OS为14个月,中位PFS为8个月。基线 LDH 水平升高的患者预后明显较差,中位 OS 为 9 个月,而 LDH 水平较低的患者为 20 个月;中位 PFS 为 6 个月,而 LDH 水平较低的患者为 13 个月(p 结论:LDH 水平升高的患者预后明显较差:开始使用 Stupp 方案前 LDH 水平升高具有重要的临床意义,因为这预示着胶质母细胞瘤患者的总生存期和无进展生存期较差,RR 也较差。将 LDH 测量纳入治疗计划有助于识别预后较差风险较高的患者,从而制定更有针对性、可能更具侵略性的治疗策略,改善胶质母细胞瘤的管理和治疗反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum lactate dehydrogenase as a prognostic marker for treatment response in IDH wild-type glioblastoma patients undergoing stupp protocol.

Background and aim: Elevated lactate dehydrogenase (LDH), a marker of tumor aggressiveness and metabolic alterations, may predict treatment response and overall survival across various tumors. This study investigates the correlation between serum LDH levels and clinical outcomes in glioblastoma patients treated with radiotherapy (RT) and temozolomide (TMZ).

Materials and methods: This retrospective study analysed patients with IDH wild-type glioblastoma (IDH-wt GB) treated at the Radiotherapy Department of Azienda Ospedaliero-Universitaria Senese from 2018 to 2023. Clinical data, including hematologic parameters (e.g., LDH), imaging (MRI), and MGMT promoter methylation status, were collected. All patients received RT and TMZ following the Stupp protocol. Serum LDH levels were measured one week before RT, and Radiological Response (RR) was assessed using RANO criteria. Overall survival (OS), progression-free survival (PFS), and RR were primary endpoints. Statistical analyses included Kaplan-Meier, Cox regression, and decision tree analysis for LDH cut-off determination.

Results: In a cohort of 147 IDH wild-type glioblastoma patients treated with the Stupp protocol, the median OS was 14 months and median PFS was 8 months. Elevated baseline LDH levels were associated with significantly poorer outcomes, showing a median OS of 9 months versus 20 months and a median PFS of 6 months versus 13 months for lower LDH levels (p < 0.001 and p = 0.0001, respectively). LDH levels also correlated with RR (p = 0,001), Multivariate analysis confirmed high LDH as an independent predictor of worse OS (HR = 2.31) and PFS (HR = 2.60), suggesting its utility as a prognostic biomarker.

Conclusions: Elevated LDH levels before starting the Stupp protocol are clinically significant as they predict poorer overall survival and progression-free survival in glioblastoma patients and worse RR. Incorporating LDH measurements into treatment planning can help identify patients at higher risk of poor outcomes, allowing for more tailored and potentially aggressive treatment strategies to improve management and therapeutic responses in glioblastoma.

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来源期刊
Journal of Neuro-Oncology
Journal of Neuro-Oncology 医学-临床神经学
CiteScore
6.60
自引率
7.70%
发文量
277
审稿时长
3.3 months
期刊介绍: The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.
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