[Clinical characteristics of epidermal growth factor receptor-mutated advanced adenocarcinoma transformed into small-cell lung cancer]

Zhonghua Jie He He Hu Xi Za Zhi. 2021 Aug 12;44(8):723-728. doi: 10.3760/cma.j.cn112147-20201026-01063.
[Article in Chinese]

Abstract

Objective: To explore the clinicopathological characteristics and genomic characteristics of four patients with epidermal growth factor receptor(EGFR)-mutated advanced adenocarcinoma transformed into small-cell lung cancer. Methods: Four cases of EGFR-mutated advanced adenocarcinoma of the lung transformed into small-cell lung cancer were studied by clinical data, pathological morphology, immunohistochemistry and gene detection. Result: EGFR-mutated adenocarcinoma of the lung was heterogeneous in clinical and genomic profiles, of ten characterized by RB1, TP53 and PIK3CA mutations. Its transformation into small-cell lung cancer was a particularly aggressive mechanism of drug resistance, but the machanisms were not clear NSE and other tumor indicators had low diagnostic value for transformation. Conclusions: EGFR-mutated adenocarcinoma of the lung transformed into small-cell lung cancer was one of the reasons for EGFR resistance with avery poor prognosis.

目的: 探讨表皮生长因子受体(EGFR)突变型肺腺癌向小细胞肺癌(SCLC)转化患者的临床和基因组学特点。 方法: 报道4例EGFR突变的肺腺癌转化为SCLC患者的临床资料、病理形态、免疫组织化学和基因检测结果,结合文献对其进行探讨。 结果: EGFR突变型肺腺癌在临床表现和基因组学上具有异质性,患者常以RB1、TP53、PIK3CA等突变为主要特征,但具体转化机制仍不明确,神经元特异性烯醇化酶(NSE)等肿瘤指标对转化的诊断价值不高,转化后即使EGFR突变仍然存在,EGFR酪氨酸激酶抑制剂(EGFR-TKi)治疗也无效。 结论: EGFR突变的肺腺癌转化为SCLC是EGFR-TKi耐药的原因之一,是一种特别具有攻击性的靶外耐药机制,预后较差。.

MeSH terms

  • Adenocarcinoma* / genetics
  • ErbB Receptors / genetics
  • Humans
  • Lung Neoplasms* / genetics
  • Mutation
  • Protein Kinase Inhibitors

Substances

  • Protein Kinase Inhibitors
  • ErbB Receptors