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恩曲替尼治疗 NTRK1 重排非小细胞肺癌的持久临床应答。

Durable Clinical Response to Entrectinib in NTRK1-Rearranged Non-Small Cell Lung Cancer.

机构信息

*Department of Medicine, Massachusetts General Hospital, Boston, MA; †Department of Pathology, Massachusetts General Hospital, Boston, MA; ‡Memorial Sloan Kettering Cancer Center, New York, NY; ‖Sarah Cannon Research Institute/Florida Cancer Specialists, Sarasota, FL; §Sarah Cannon Research Institute/Tennessee Oncology, PLLC, Nashville, TN; ¶Department of Medicine, Georgetown University Medical Center, Washington, DC; #University of California Irving Health, Orange, CA; **Dana-Farber Cancer Institute, Boston, MA; ††Beth Israel Deaconess Medical Center, Boston, MA; and ‡‡Ignyta, Inc., San Diego, CA.

出版信息

J Thorac Oncol. 2015 Dec;10(12):1670-4. doi: 10.1097/01.JTO.0000473485.38553.f0.

Abstract

INTRODUCTION

Chromosomal rearrangements involving neurotrophic tyrosine kinase 1 (NTRK1) occur in a subset of non-small cell lung cancers (NSCLCs) and other solid tumor malignancies, leading to expression of an oncogenic TrkA fusion protein. Entrectinib (RXDX-101) is an orally available tyrosine kinase inhibitor, including TrkA. We sought to determine the frequency of NTRK1 rearrangements in NSCLC and to assess the clinical activity of entrectinib.

METHODS

We screened 1378 cases of NSCLC using anchored multiplex polymerase chain reaction (AMP). A patient with an NTRK1 gene rearrangement was enrolled onto a Phase 1 dose escalation study of entrectinib in adult patients with locally advanced or metastatic tumors (NCT02097810). We assessed safety and response to treatment.

RESULTS

We identified NTRK1 gene rearrangements at a frequency of 0.1% in this cohort. A patient with stage IV lung adenocrcinoma with an SQSTM1-NTRK1 fusion transcript expression was treated with entrectinib. Entrectinib was well tolerated, with no grade 3-4 adverse events. Within three weeks of starting on treatment, the patient reported resolution of prior dyspnea and pain. Restaging CT scans demonstrated a RECIST partial response (PR) and complete resolution of all brain metastases. This patient has continued on treatment for over 6 months with an ongoing PR.

CONCLUSIONS

Entrectinib demonstrated significant anti-tumor activity in a patient with NSCLC harboring an SQSTM1-NTRK1 gene rearrangement, indicating that entrectinib may be an effective therapy for tumors with NTRK gene rearrangements, including those with central nervous system metastases.

摘要

简介

神经酪氨酸激酶 1(NTRK1)的染色体重排发生在一小部分非小细胞肺癌(NSCLC)和其他实体瘤恶性肿瘤中,导致致癌 TrkA 融合蛋白的表达。恩曲替尼(RXDX-101)是一种口服酪氨酸激酶抑制剂,包括 TrkA。我们旨在确定 NSCLC 中 NTRK1 重排的频率,并评估恩曲替尼的临床活性。

方法

我们使用锚定多重聚合酶链反应(AMP)筛选了 1378 例 NSCLC 病例。一名患有 NTRK1 基因重排的患者被纳入成人局部晚期或转移性肿瘤(NCT02097810)中恩曲替尼的 1 期剂量递增研究。我们评估了安全性和治疗反应。

结果

我们在该队列中发现 NTRK1 基因重排的频率为 0.1%。一名患有 SQSTM1-NTRK1 融合转录本表达的 IV 期肺腺癌患者接受了恩曲替尼治疗。恩曲替尼耐受良好,无 3-4 级不良事件。开始治疗后三周内,患者报告先前呼吸困难和疼痛缓解。重新分期 CT 扫描显示 RECIST 部分缓解(PR)和所有脑转移灶完全消退。该患者继续接受治疗超过 6 个月,持续 PR。

结论

恩曲替尼在携带 SQSTM1-NTRK1 基因重排的 NSCLC 患者中显示出显著的抗肿瘤活性,表明恩曲替尼可能是 NTRK 基因重排肿瘤的有效治疗方法,包括有中枢神经系统转移的肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb4/4643748/49d294530f61/jto-10-1670-g001.jpg

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