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非小细胞肺癌转化为小细胞肺癌的特征及其对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)的反应:病例报告

Characterization of non-small cell lung cancer transforming to small cell lung cancer and its response to EGFR-TKI: a case report.

作者信息

Fang Guotao, Liu Weiwei, Shang Yanhong, Huo Ran, Shi Xiaoliang, Wang Yanan, Li Jinghua

机构信息

Department of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, China.

Hebei Key Laboratory of Cancer Radiotherapy and Chemotherapy, Baoding, China.

出版信息

Ann Transl Med. 2022 Jan;10(2):115. doi: 10.21037/atm-21-6991.

Abstract

Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) have demonstrated significant survival benefits for advanced non-small cell lung cancer (NSCLC) patients with sensitive EGFR mutations. However, patients with EGFR-TKI treatment often develop acquired resistance subsequently. Transformation from NSCLC to small cell lung cancer (SCLC) is a rare EGFR-TKI resistance mechanism for patients with sensitive mutations. Herein, we report a NSCLC patient with exon 19 deletion treated with EGFR-TKI. During treatment, the pathological type of tumor showed transformation from NSCLC to combined SCLC and then to pure SCLC after acquiring EGFR-TKI resistance. Genomic analysis revealed that the exon 19 deletion, Y220H mutation, and retinoblastomal transcriptional corepressor 1 () F755V mutation existed persistently. Immunohistochemical results showed the loss of EGFR and RB1 expression in SCLC. The patient received multi-line chemotherapy with platinum agents and experienced a briefly effective window, but died of aggressive tumor progression. We profiled the transformation from NSCLC to SCLC of this case and pointed out the importance of repeat biopsy in response to EGFR-TKI resistance. Our results showed a novel RB1 F755V mutation which may be associated with RB1 loss. This report summarized the clinical characteristics, mechanisms, and predictors of SCLC transformation, and discussed the treatment after transformation.

摘要

表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)已证明对具有敏感EGFR突变的晚期非小细胞肺癌(NSCLC)患者有显著的生存益处。然而,接受EGFR-TKI治疗的患者随后常出现获得性耐药。从NSCLC转化为小细胞肺癌(SCLC)是具有敏感突变患者罕见的EGFR-TKI耐药机制。在此,我们报告1例接受EGFR-TKI治疗的19外显子缺失的NSCLC患者。治疗期间,肿瘤病理类型显示在获得EGFR-TKI耐药后从NSCLC转化为SCLC合并型,然后转变为纯SCLC。基因组分析显示19外显子缺失、Y220H突变和成视网膜细胞瘤转录共抑制因子1(RB1)F755V突变持续存在。免疫组化结果显示SCLC中EGFR和RB1表达缺失。该患者接受了含铂药物的多线化疗,经历了短暂的有效窗口,但死于侵袭性肿瘤进展。我们分析了该病例从NSCLC到SCLC的转化情况,并指出了针对EGFR-TKI耐药进行重复活检的重要性。我们的结果显示了一种可能与RB1缺失相关的新的RB1 F755V突变。本报告总结了SCLC转化的临床特征、机制和预测因素,并讨论了转化后的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/071d/8848416/e12618e2d86f/atm-10-02-115-f1.jpg

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