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小细胞肺癌转化与T790M突变:一例在EGFR突变型肺腺癌的肿瘤再活检及血浆样本中检测到两种TKI耐药获得性机制的病例报告

Small cell lung cancer transformation and the T790M mutation: A case report of two acquired mechanisms of TKI resistance detected in a tumor rebiopsy and plasma sample of EGFR-mutant lung adenocarcinoma.

作者信息

Alì Greta, Bruno Rossella, Giordano Mirella, Prediletto Irene, Marconi Letizia, Zupo Simonetta, Fedeli Franco, Ribechini Alessandro, Chella Antonio, Fontanini Gabriella

机构信息

Unit of Pathological Anatomy, University Hospital of Pisa, I-56126 Pisa, Italy.

Department of Surgical, Medical and Molecular Pathology and Critical Area, University of Pisa, I-56126 Pisa, Italy.

出版信息

Oncol Lett. 2016 Nov;12(5):4009-4012. doi: 10.3892/ol.2016.5193. Epub 2016 Sep 26.

DOI:10.3892/ol.2016.5193
PMID:27895763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5104225/
Abstract

The present study describes the case of a 45-year-old man diagnosed with metastatic lung adenocarcinoma, which harbored a deletion within exon 19 of the epidermal growth factor receptor () gene. The patient was subsequently treated with gefitinib (250 mg/day orally from May 2013 to March 2014), but developed acquired resistance to the drug following 11 months of treatment. Tumor burden molecular analysis was performed on a tumor rebiopsy and plasma sample, and histological analysis was also performed on the tumor rebiopsy. A small cell transformation retaining the original mutation was detected in the tumor rebiopsy, while the T790M mutation together with the activating ex19del mutation were identified only in the plasma sample. The patient was treated with cytotoxic chemotherapy (off-label schedule with epirubicin 80 mg/mq and paclitaxel 160 mg/mq every 21 days for 6 cycles) and radiation (50.4 Gy administered in 28 fractions of 1.8 Gy once daily for 5.5 weeks) specific for small cell lung cancer, and may also have benefitted from treatment with a third generation T790M-specific EGFR-TKI. To better describe the mechanisms of resistance to TKI inhibitors and to optimize therapeutic regimens, the simultaneous analysis of tumor biopsies and circulating tumor DNA should be considered.

摘要

本研究描述了一名45岁男性被诊断为转移性肺腺癌的病例,该患者的表皮生长因子受体(EGFR)基因第19外显子存在缺失。该患者随后接受吉非替尼治疗(2013年5月至2014年3月口服250毫克/天),但在治疗11个月后对该药物产生了获得性耐药。对肿瘤再次活检样本和血浆样本进行了肿瘤负荷分子分析,同时也对肿瘤再次活检样本进行了组织学分析。在肿瘤再次活检中检测到保留原始EGFR突变的小细胞转化,而仅在血浆样本中鉴定出T790M突变以及激活的外显子19缺失突变。该患者接受了针对小细胞肺癌的细胞毒性化疗(非标准方案,表柔比星80毫克/平方米和紫杉醇160毫克/平方米,每21天一次,共6个周期)和放疗(50.4 Gy,分28次,每次1.8 Gy,每天一次,共5.5周),并且可能也从第三代T790M特异性EGFR-TKI治疗中获益。为了更好地描述对TKI抑制剂的耐药机制并优化治疗方案,应考虑同时分析肿瘤活检样本和循环肿瘤DNA。

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