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携带有间充质-上皮转化因子外显子 14 跳跃突变的肺腺癌患者对克唑替尼和卡博替尼的反应:一例报告。

Responses to crizotinib and cabozantinib in patient with lung adenocarcinoma harboring mesenchymal-epithelial transition factor exon 14 skipping mutation: A case report.

机构信息

Department of Oncology.

Department of Pulmonary Medicine, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Medicine (Baltimore). 2021 Jan 29;100(4):e24300. doi: 10.1097/MD.0000000000024300.

Abstract

RATIONALE

Lung cancer is a leading cause of cancer-related mortality worldwide. Currently, targeted therapy has proved highly efficient in the treatment of advanced non-small cell lung cancer (NSCLC). Mesenchymal-epithelial transition factor (MET) is considered a validated molecular target in NSCLC. Given the low incidence of MET exon 14 skipping mutation, the planning of precision treatment for patients is a clinical problem that needs to be solved. In this report, we present a MET-positive case that benefited from crizotinib and cabozantinib treatment.

PATIENT CONCERNS

A 77-year-old patient was diagnosed with lung adenocarcinoma in our hospital. Positron emission tomography-computed tomography (PET-CT) showed a right upper lobe mass (58 × 56 mm, SUVmax 15.6), right hilar enlarged lymph nodes, and multiple bone and left adrenal metastases (c-T3N1M1c).

DIAGNOSES

MET exon 14 mutation (exon14, c.2888-1G>C) was examined using the lung puncture sample by next generation sequencing. Therefore, the patient was diagnosed with late-stage lung adenocarcinoma with MET exon14 skipping gene mutation.

INTERVENTIONS

Crizotinib was given as the first-line treatment from August 2019. Considering the resistance of crizotinib, cabozantinib was given for second-line treatment.

OUTCOMES

Crizotinib was administered (250 mg bid) for 8 months, and her disease achieved partial regression (PR) and progression-free survival (PFS), which lasted for 8 months. The patient also reached PR after the second-line treatment with cabozantinib, and is currently under follow-up, with an overall survival (OS) of >12 months.

LESSONS

As MET exon 14 skipping mutation is rare in clinical practices, MET-TKIs (tyrosine kinase inhibitors) treatment can boost curative effects and improve prognosis of patients with advanced lung adenocarcinoma. This case report supports a rationale for the treatment of lung adenocarcinoma patients with a MET exon 14 skipping mutation and provides alternative treatment options for these types of NSCLC patients.

摘要

背景

肺癌是全球癌症相关死亡的主要原因。目前,靶向治疗已被证明在治疗晚期非小细胞肺癌(NSCLC)方面非常有效。间质上皮转化因子(MET)被认为是 NSCLC 的一个经过验证的分子靶点。鉴于 MET 外显子 14 跳跃突变的发生率较低,规划患者的精准治疗是一个需要解决的临床问题。在本报告中,我们报告了一例 MET 阳性患者,该患者从克唑替尼和卡博替尼治疗中获益。

病例概述

一名 77 岁患者在我院被诊断为肺腺癌。正电子发射断层扫描-计算机断层扫描(PET-CT)显示右上肺肿块(58×56mm,SUVmax 15.6),右肺门淋巴结肿大,以及多处骨和左肾上腺转移(c-T3N1M1c)。

检查

通过肺部穿刺样本进行下一代测序检查到 MET 外显子 14 突变(exon14,c.2888-1G>C)。因此,患者被诊断为晚期肺腺癌合并 MET 外显子 14 跳跃基因突变。

治疗

从 2019 年 8 月开始,给予克唑替尼作为一线治疗。考虑到克唑替尼的耐药性,给予卡博替尼作为二线治疗。

结果

患者接受克唑替尼(bid 250mg)治疗 8 个月,疾病达到部分缓解(PR)和无进展生存期(PFS),持续 8 个月。二线治疗用卡博替尼后,患者也达到 PR,目前正在随访中,总生存期(OS)>12 个月。

结论

由于 MET 外显子 14 跳跃突变在临床上较为罕见,MET-TKIs(酪氨酸激酶抑制剂)治疗可提高晚期肺腺癌患者的疗效并改善预后。本病例报告支持对 MET 外显子 14 跳跃突变的肺腺癌患者进行治疗,并为这些类型的 NSCLC 患者提供了替代治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f71/7850643/873ed4b3eea1/medi-100-e24300-g001.jpg

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