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中枢神经系统血液系统恶性肿瘤的紧急和急诊放疗:文献综述与实践方法

英文原题:Urgent and emergent radiotherapy for hematologic malignancies of the central nervous system: a review of the literature and practical approach.

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Urgent and emergent radiotherapy for hematologic malignancies of the central nervous system: a review of the literature and practical approach.

PubMed 2025/03/31(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

RT 是实现血液系统恶性肿瘤快速缓解的有力工具,因此在紧急神经系统情况下应早期考虑。全面的检查和与多学科团队的讨论对于将 RT 最佳地整合到其他 CNS 穿透性治疗的背景下至关重要。在新疗法的背景下,进一步明确 RT 靶区体积的工作是必要的。

研究思路结论见上方概要

血液系统恶性肿瘤,包括白血病、淋巴瘤和骨髓瘤,可在诊断时或复发后期累及中枢神经系统(CNS)。CNS受累可导致需要及时评估和治疗的急性神经系统症状或体征。放疗(RT)可带来快速的疾病缓解,但在紧急临床情况下,如何最好地将其早期纳入多模式治疗往往尚不明确。

在此,我们概述了对累及CNS的血液系统恶性肿瘤患者进行紧急RT规划和整合的实用方法。我们提供了文献综述,以根据组织学和临床情况为RT的适应症、时机、剂量和治疗体积提供依据。我们还强调了该领域不断演变的争议,以及RT与新型疗法联合应用的日益增多的适应症。

RT 通常是挽救颅神经病变或神经功能缺损最快、最可靠的手段,应尽早考虑。如果预期全身治疗或鞘内治疗作为初始治疗能够迅速起效,仍应规划模拟定位,以防疗效延迟而需要 RT。RT 与某些全身治疗或鞘内治疗联合可能导致不可接受的神经毒性;因此,早期多学科讨论以合理安排治疗顺序至关重要。通过全身影像学、完整神经轴 MRI、眼科检查和脑脊液采样进行全面评估,可以确定从局部 RT 到全中枢神经系统照射(CSI)的靶区范围。剂量可从惰性疾病低至 4 Gray(Gy),到更具侵袭性或难治性疾病 36-50 Gy。通常可考虑在治疗中途重新规划,以应对肿瘤体积迅速缩小,从而改善治疗窗。RT 在将症状性患者桥接至新型治疗(如CAR-T 细胞治疗)方面具有前景,但最佳剂量和治疗体积仍是不断发展的课题,需要进一步前瞻性评估。

展开英文摘要原文

Here, we outline a practical approach to planning and incorporating urgent RT in patients with hematologic malignancies involving the CNS. We provide a review of the literature to inform RT indications, timing, dosing, and treatment volumes by histology and clinical scenario. We also highlight evolving controversies in this field and growing indications for RT in conjunction with novel therapeutics.

RT is often the quickest-acting, most reliable tool to salvage cranial neuropathies or neurologic deficits and should be considered early. If systemic or intrathecal therapy are expected to achieve swift response as upfront treatment, simulation should still be planned in the event that response is delayed and RT is needed. RT in combination with certain systemic or intrathecal therapies can lead to unacceptable neurotoxicity; therefore, early multidisciplinary discussion to appropriately sequence therapies is critical. Thorough work-up with systemic imaging, complete neuroaxis MRI, ophthalmologic exam, and cerebrospinal fluid sampling can dictate target volumes from focal RT to comprehensive craniospinal irradiation (CSI). Dosing can range from as low as 4 Gray (Gy) for indolent disease to 36-50 Gy for more aggressive or refractory disease. Often, mid-treatment re-planning can be considered to address swift volume reduction to improve the therapeutic window. RT plays a promising role for bridging symptomatic patients to novel therapeutics (e.g., chimeric antigen receptor T-cell therapy), but optimal dosing and treatment volumes are evolving topics that require further prospective evaluation.

RT is a powerful tool for achieving rapid responses in hematologic malignancies and therefore should be considered early in urgent neurologic settings. Thorough workup and discussions with the multi-disciplinary team are critical to best incorporate RT in the context of other CNS-penetrating therapies. Further work is warranted on defining RT target volumes in the context of novel therapeutics.

论文信息

作者
Tringale KR、Imber BS、Cederquist GY、Yahalom J、Moore ZR、Hoppe RT、Binkley MS、Ross JB
第一作者单位
Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, United States.United States
通讯作者单位
Department of Radiation Oncology, Stanford University, Palo Alto, CA, United States.United States
文献类型
综述
期刊
Frontiers in oncology2025
原文标识
PubMed 40231259 · DOI 10.3389/fonc.2025.1511261