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病例报告:波齐替尼对携带EGFR外显子20插入突变的转移性非小细胞肺癌患者的显著疗效。

Case Report: Exceptional Response to Poziotinib in Patient with Metastatic Non-Small Cell Lung Cancer With EGFR Exon 20 Insertion Mutation.

作者信息

Prelaj Arsela, Bottiglieri Achille, Bhat Gajanan, Washington Rocky, Calareso Giuseppina, Greco Gabriella Francesca, Ferrara Roberto, Brambilla Marta, De Toma Alessandro, Occhipinti Mario, Manglaviti Sara, Soro Alberto, Ganzinelli Monica, Lo Russo Giuseppe, Proto Claudia

机构信息

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.

出版信息

Front Oncol. 2022 Jun 8;12:902967. doi: 10.3389/fonc.2022.902967. eCollection 2022.

Abstract

Among the several next-generation tyrosine kinase inhibitors (TKIs) tested against uncommon EFGR alterations, poziotinib has been demonstrated to be a powerful agent for metastatic non-small-cell lung cancer (mNSCLC) with aberrations in exon 20, and FDA approval is being sought in the previously-treated population. Poziotinib has also shown activity in mNSCLC with aberrations in EGFR exon 20. Herein, we report the first published case of a patient affected by mNSCLC harbouring an exon 20 insertion (EGFRex20ins) mutation who achieved a complete response (CR) under treatment with poziotinib as part of the ZENITH20 trial. In January 2021, a former smoker 62-year-old female patient was diagnosed with relapse, after two surgeries and post-operative chemotherapy of mNSCLC, at liver and retroperitoneal nodes. Given the identification by Next Generation Sequencing (NGS) of EGFRex20ins mutation, she was enrolled in ZENITH20-cohort 5 trial, a phase 2 multicentre study aimed to assess the efficacy and safety of poziotinib in patients with EGFR or HER2 exon 20 insertion mutations. Poziotinib as first-line systemic therapy for metastatic disease was initiated at the end of January 2021 and administrated at the initial dosage of 8 mg orally twice daily (BID). The most common side effects from the beginning of the treatment included alopecia, macular skin rash, diarrhoea, xerostomia, and conjunctivitis. Due to these adverse events, poziotinib was discontinued during the first 3 months and then reduced to 6 mg orally BID in April 2021. After the dose de-escalation, the adverse events ameliorated, and the patient better tolerated the treatment without further interruption. Since the first reevaluation (after 4 weeks of therapy), the treatment with poziotinib resulted to be remarkably effective, with a partial response (PR) subsequently confirmed in May and July 2021. Then, in October 2021, a CT scan confirmed a CR, maintained with good tolerance at the last reevaluation in February 2022. Treatment is still ongoing at the same dosage. In this case, poziotinib has represented a successful and well-tolerated first-line treatment alternative to chemotherapy in this patient with EGFR exon 20 insertion mutated mNSCLC.

摘要

在针对罕见表皮生长因子受体(EGFR)改变进行测试的几种下一代酪氨酸激酶抑制剂(TKI)中,波齐替尼已被证明是一种对第20外显子有畸变的转移性非小细胞肺癌(mNSCLC)有效的药物,目前正在寻求美国食品药品监督管理局(FDA)对先前接受过治疗的患者群体的批准。波齐替尼在EGFR第20外显子有畸变的mNSCLC中也显示出活性。在此,我们报告了首例公开的携带第20外显子插入(EGFRex20ins)突变的mNSCLC患者病例,该患者在作为ZENITH20试验一部分接受波齐替尼治疗后实现了完全缓解(CR)。2021年1月,一名62岁的曾吸烟女性患者在接受两次手术及mNSCLC术后化疗后,被诊断为肝脏和腹膜后淋巴结复发。鉴于通过下一代测序(NGS)鉴定出EGFRex20ins突变,她被纳入ZENITH20队列5试验,这是一项2期多中心研究,旨在评估波齐替尼对EGFR或HER2第20外显子插入突变患者的疗效和安全性。2021年1月底开始将波齐替尼作为转移性疾病的一线全身治疗药物,初始剂量为每日两次口服8毫克(BID)。从治疗开始最常见的副作用包括脱发、黄斑皮疹、腹泻、口干和结膜炎。由于这些不良事件,波齐替尼在最初3个月内停药,然后在2021年4月减至每日两次口服6毫克。剂量降低后,不良事件有所改善,患者对治疗的耐受性更好,未再进一步中断治疗。自首次重新评估(治疗4周后)以来,波齐替尼治疗效果显著,随后在2021年5月和7月确认部分缓解(PR)。然后,在2021年10月,CT扫描确认达到CR,在2022年2月的最后一次重新评估中耐受性良好。目前仍以相同剂量继续治疗。在该病例中,对于这位携带EGFR第20外显子插入突变的mNSCLC患者,波齐替尼是一种成功且耐受性良好的替代化疗的一线治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7497/9215205/bab9aa05f194/fonc-12-902967-g001.jpg

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