TUM School of Medicine, Department of Radiation Oncology, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Strahlenther Onkol. 2024 Apr;200(4):259-275. doi: 10.1007/s00066-024-02202-0. Epub 2024 Mar 15.
The aim of this review was to evaluate the existing evidence for radiotherapy for brain metastases in breast cancer patients and provide recommendations for the use of radiotherapy for brain metastases and leptomeningeal carcinomatosis.
For the current review, a PubMed search was conducted including articles from 01/1985 to 05/2023. The search was performed using the following terms: (brain metastases OR leptomeningeal carcinomatosis) AND (breast cancer OR breast) AND (radiotherapy OR ablative radiotherapy OR radiosurgery OR stereotactic OR radiation).
Despite the fact that the biological subtype of breast cancer influences both the occurrence and relapse patterns of breast cancer brain metastases (BCBM), for most scenarios, no specific recommendations regarding radiotherapy can be made based on the existing evidence. For a limited number of BCBM (1-4), stereotactic radiosurgery (SRS) or fractionated stereotactic radiotherapy (SRT) is generally recommended irrespective of molecular subtype and concurrent/planned systemic therapy. In patients with 5-10 oligo-brain metastases, these techniques can also be conditionally recommended. For multiple, especially symptomatic BCBM, whole-brain radiotherapy (WBRT), if possible with hippocampal sparing, is recommended. In cases of multiple asymptomatic BCBM (≥ 5), if SRS/SRT is not feasible or in disseminated brain metastases (> 10), postponing WBRT with early reassessment and reevaluation of local treatment options (8-12 weeks) may be discussed if a HER2/Neu-targeting systemic therapy with significant response rates in the central nervous system (CNS) is being used. In symptomatic leptomeningeal carcinomatosis, local radiotherapy (WBRT or local spinal irradiation) should be performed in addition to systemic therapy. In patients with disseminated leptomeningeal carcinomatosis in good clinical condition and with only limited or stable extra-CNS disease, craniospinal irradiation (CSI) may be considered. Data regarding the toxicity of combining systemic therapies with cranial and spinal radiotherapy are sparse. Therefore, no clear recommendations can be given, and each case should be discussed individually in an interdisciplinary setting.
本综述旨在评估乳腺癌患者脑转移放疗的现有证据,并为脑转移和软脑膜癌病的放疗提供建议。
为了进行本次综述,我们在 PubMed 上进行了搜索,包括 1985 年 1 月至 2023 年 5 月的文章。搜索使用了以下术语:(脑转移或软脑膜癌病)和(乳腺癌或乳房)和(放疗或消融放疗或放射外科或立体定向或放疗)。
尽管乳腺癌脑转移(BCBM)的生物学亚型既影响其发生又影响其复发模式,但就大多数情况而言,基于现有证据,无法针对放疗提出具体建议。对于有限数量的 BCBM(1-4),无论分子亚型和同时/计划的全身治疗如何,通常建议采用立体定向放射外科(SRS)或分次立体定向放疗(SRT)。对于 5-10 个寡发性脑转移,这些技术也可以有条件地推荐。对于多发性、特别是有症状的 BCBM,建议使用全脑放疗(WBRT),如果可能,伴有海马保护。对于多发性无症状 BCBM(≥5),如果不能进行 SRS/SRT 或存在播散性脑转移(>10),如果正在使用中枢神经系统(CNS)反应率高的 HER2/Neu 靶向全身治疗,则可以讨论延迟 WBRT,同时重新评估局部治疗选择(8-12 周)。对于有症状的软脑膜癌病,除了全身治疗外,还应进行局部放疗(WBRT 或局部脊柱照射)。对于临床状况良好且仅有有限或稳定的颅外疾病的播散性软脑膜癌病患者,可考虑进行颅脊髓照射(CSI)。关于将全身治疗与颅部和脊髓放疗相结合的毒性数据很少。因此,无法给出明确的建议,每个病例都应在跨学科环境中进行单独讨论。