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曲妥珠单抗德鲁替康与立体定向放射外科治疗HER2阳性和HER2低表达乳腺癌脑转移的多机构报告。

Multi-institutional report of trastuzumab deruxtecan and stereotactic radiosurgery for HER2 positive and HER2-low breast cancer brain metastases.

作者信息

Khatri Vaseem M, Mestres-Villanueva Mariella A, Yarlagadda Sreenija, Doniparthi Ajay, Smith David B, Nakashima Justyn Y, Bryant John M, Zhao Dekuang, Upadhyay Rituraj, Mills Matthew N, Oliver Daniel E, Yu Hsiang-Hsuan Michael, Palmer Joshua D, Williams Nicole O, Mahtani Reshma L, Ahluwalia Manmeet S, Soliman Hatem H, Han Hyo S, Soyano Aixa E, Kim Youngchul, Kotecha Rupesh, Beyer Sasha J, Ahmed Kamran A

机构信息

Department of Radiation Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.

Department of Radiation Oncology, The Ohio State University Wexner Medical Center, Columbus, OH, 43201, USA.

出版信息

NPJ Breast Cancer. 2024 Nov 21;10(1):100. doi: 10.1038/s41523-024-00711-w.

Abstract

Trastuzumab-deruxtecan (T-DXd) has demonstrated intracranial efficacy; however, safety and efficacy data remains limited with stereotactic radiosurgery (SRS). A multi-institutional review was performed with HER2+ or HER2-low metastatic breast cancer treated with T-DXd and SRS for active brain metastases. We identified 215 lesions treated over 48 SRS courses in 34 patients. Median follow up from T-DXd initiation was 13.9 months. The cumulative incidence of symptomatic radiation necrosis at 24 months per lesion was 2.1% and per patient 11%. The 12-month LC was 97%. HER2-low was associated with worse distant intracranial control (DIC) (adjusted HR 2.5, 95% CI 1.1-5.6, p = 0.03) and worse systemic progression free survival (PFS) (HR 4.1, 95% CI 1.6-10.7, p = 0.004). Concurrent SRS and T-DXd has excellent local control, without an increased risk of radiation necrosis. HER2-low disease is associated with worse systemic PFS and DIC with T-DXd compared to HER2+.

摘要

曲妥珠单抗-德曲妥珠单抗(T-DXd)已显示出颅内疗效;然而,立体定向放射外科(SRS)的安全性和疗效数据仍然有限。对接受T-DXd和SRS治疗活动性脑转移的HER2阳性或HER2低表达转移性乳腺癌患者进行了多机构回顾性研究。我们在34例患者的48个SRS疗程中确定了215个病灶。从开始使用T-DXd起的中位随访时间为13.9个月。每个病灶在24个月时症状性放射性坏死的累积发生率为2.1%,每位患者为11%。12个月的局部控制率为97%。HER2低表达与较差的远处颅内控制(DIC)(校正风险比2.5,95%置信区间1.1-5.6,p=0.03)和较差的全身无进展生存期(PFS)(风险比4.1,95%置信区间1.6-10.7,p=0.004)相关。SRS与T-DXd联合应用具有出色的局部控制效果,且放射性坏死风险未增加。与HER2阳性疾病相比,HER2低表达疾病使用T-DXd时全身PFS和DIC较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/345d/11582691/d581087ce2bc/41523_2024_711_Fig1_HTML.jpg

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