Department of Hematological, Pneumological and Cardiovascular Sciences - Section of Pneumology, University and Fondazione IRCCS Policlinico San Matteo 27100 Pavia, Italy.
J Cancer. 2011;2:474-7. doi: 10.7150/jca.2.474. Epub 2011 Sep 23.
We discuss the case of synchronous bilateral lung cancers which feature the same histological phenotype and a different EGFR mutational profile. Both histological and molecular characterizations were performed on specimens derived thorough CT-guided fine needle aspiration. A first-line chemotherapy was unsuccessful. Subsequent objective response to the EGFR inhibitor Erlotinib was clearly coherent with the sequencing data and the mutated nodule was effectively reduced (> 50%) after therapy, while the lesion assessed as EGFR wild type featured a slight response. This report has two relevant implications. It points out that in case of multiple malignant lesions at time of diagnosis, molecular profiling should be as extensive as possible and it might contribute to clarify the association between the lesions found. Besides the molecular analysis on cytology specimens could identify an accurate and safe diagnostic approach for clinical use.
我们讨论了一例同时性双侧肺癌病例,其具有相同的组织学表型和不同的 EGFR 突变谱。组织学和分子特征均通过 CT 引导下的细针抽吸获得的标本进行。一线化疗无效。随后对 EGFR 抑制剂厄洛替尼的客观反应与测序数据明显一致,治疗后突变结节有效减少(>50%),而评估为 EGFR 野生型的病变仅略有反应。本报告有两个相关的意义。它指出,在诊断时存在多个恶性病变的情况下,分子谱分析应尽可能广泛,这有助于阐明发现的病变之间的关联。此外,细胞学标本的分子分析可以为临床应用提供准确、安全的诊断方法。