trastuzumab-deruxtecan和脑立体定向放射外科术后临床显著的放射坏死:癌症患者的病例系列

IF 0.2 Q4 ONCOLOGY
Victoria Wytiaz , Anne Schott , Aki Morikawa , Michelle M. Kim
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引用次数: 0

摘要

据估计,在美国有15%的乳腺癌患者过度表达人表皮生长因子受体2 (HER2), HER2阳性乳腺癌患者发生脑转移的风险增加。最近开发的her2靶向药物,包括曲妥珠单抗德鲁替康(T-DXd),已经改善了全身性疾病控制,包括转移到脑部的疾病。由于许多脑转移患者既接受了T-DXd,也接受了脑立体定向放射手术(SRS),因此探索这些治疗方式的相互作用是很重要的。在这里,我们报告了两例临床显著的放射性坏死(CSRN)发生在治疗史包括脑SRS和T-DXd的转移性乳腺癌患者中。我们还简要描述了另外两例在T-DXd之前有曲妥珠单抗emtansine (T-DM1)远程治疗史的患者的CSRN,因为T-DM1也被报道导致HER2+转移性乳腺癌患者的CSRN发生率增加,这些患者有srs治疗的脑转移史。虽然病例报告和系列报道已经说明了T-DM1的这种现象,但没有现有文献描述T-DXd的这些发现。我们描述了这些病例,并回顾了这一特定患者群体中CSRN的潜在病因,从而强调需要更彻底地了解由治疗方式交叉引起的潜在不良事件,即脑SRS和her2导向的抗体-药物偶联物,因为靶向治疗的前景不断发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinically significant radiation necrosis following trastuzumab-deruxtecan and brain stereotactic radiosurgery: A case series in breast cancer patients

An estimated 15% of breast cancers in the United States overexpress human epidermal growth factor receptor 2 (HER2), and patients with HER2+ breast cancer have an increased risk of developing brain metastases. The recent development of HER2-targeted agents, including trastuzumab deruxtecan (T-DXd), has resulted in improved systemic disease control, including disease metastasized to the brain. Because many patients with brain metastases have received both T-DXd and have also undergone brain stereotactic radiosurgery (SRS), it is important to explore the interaction of these treatment modalities. Here, we present two cases of clinically significant radiation necrosis (CSRN) occurring in patients with metastatic breast cancer with a treatment history including brain SRS and T-DXd. We also briefly describe two additional cases of CSRN in patients with the additional remote treatment history of trastuzumab emtansine (T-DM1) prior to T-DXd, as T-DM1 has also been reported to cause increased rates of CSRN in patients with HER2+ metastatic breast cancer with a history of SRS-treated brain metastases. While case reports and series have illustrated this phenomenon with T-DM1, no existing literature has described these findings with T-DXd. We describe these cases and review the potential etiologies for CSRN in this specific patient population, thus highlighting the need for a more thorough understanding of the potential adverse events caused by the intersection of treatment modalities, namely brain SRS and HER2-directed antibody-drug conjugates as the landscape of targeted therapies continues to evolve.

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