Symptomatic CNS Radiation Necrosis Requiring Neurosurgical Resection During Treatment with Lorlatinib in ALK-Rearranged NSCLC: A Report of Two Cases.

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2020-01-14 eCollection Date: 2020-01-01 DOI:10.2147/LCTT.S224991
Viola W Zhu, Misako Nagasaka, Takafumi Kubota, Kunil Raval, Natasha Robinette, Octavio Armas, Wajd Al-Holou, Sai-Hong Ignatius Ou
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引用次数: 8

Abstract

Central nervous system (CNS) metastasis carries a significant morbidity and mortality in anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). Next-generation ALK tyrosine kinase inhibitors (TKIs) are highly CNS-penetrant and have demonstrated remarkable intracranial activity across clinical studies, and yet radiation remains the mainstay of treatment modality against CNS metastasis. We have previously reported alectinib can induce CNS radiation necrosis even after a remote history of radiation (7 years post-radiation). Lorlatinib is another potent next-generation ALK TKI that can overcome many ALK resistance mutations and has been shown to have excellent activity in patients with baseline CNS metastasis. Here we report two ALK-rearranged NSCLC patients who developed radiation necrosis shortly after initiating lorlatinib following progression on the sequential treatment of crizotinib, alectinib, and brigatinib. In both cases, radiation necrosis is evidenced by serial MRI images and histological examination of the resected CNS metastasis that had previously been radiated. Our cases highlight the importance of recognizing CNS radiation necrosis that may mimic disease progression in ALK-rearranged NSCLC treated with and potentially precipated by next-generation ALK TKIs.

Abstract Image

Abstract Image

Lorlatinib治疗alk重排非小细胞肺癌时出现症状性中枢神经系统放射性坏死需要神经外科切除:两例报告。
中枢神经系统(CNS)转移在间变性淋巴瘤激酶(ALK)重排非小细胞肺癌(NSCLC)中具有显著的发病率和死亡率。下一代ALK酪氨酸激酶抑制剂(TKIs)具有高度的中枢神经系统渗透性,并且在临床研究中显示出显著的颅内活性,然而放射治疗仍然是对抗中枢神经系统转移的主要治疗方式。我们以前报道过阿勒替尼可以诱导中枢神经系统放射性坏死,即使是在遥远的放射史(放射后7年)之后。Lorlatinib是另一种有效的下一代ALK TKI,可以克服许多ALK耐药突变,并已显示在基线中枢神经系统转移患者中具有出色的活性。在这里,我们报告了两例alk重排的NSCLC患者,他们在接受克唑替尼、阿勒替尼和布加替尼序贯治疗后不久开始氯拉替尼后发生放射性坏死。在这两种情况下,放射性坏死可通过连续MRI图像和先前放射的切除中枢神经系统转移灶的组织学检查来证明。我们的病例强调了识别中枢神经系统放射性坏死的重要性,这种坏死可能模拟用下一代ALK TKIs治疗的ALK重排非小细胞肺癌的疾病进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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