Literature DB >> 30015588

Non-Small Cell Lung Cancer with Resistance to EGFR-TKI Therapy: CT Characteristics of T790M Mutation-positive Cancer.

Hyun Jung Koo1, Mi Young Kim1, Sojung Park1, Han Na Lee1, Hwa Jung Kim1, Jae Cheol Lee1, Sang-We Kim1, Dae Ho Lee1, Chang-Min Choi1.   

Abstract

Purpose To evaluate the clinical and CT characteristics of T790M mutation-positive non-small cell lung cancer (NSCLC) after epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) therapy failure. Materials and Methods A retrospective study of 304 patients with NSCLC who underwent rebiopsy after first-line EGFR-TKI therapy was conducted. Rebiopsy methods included CT- or fluoroscopy-guided lung biopsies (n = 105), endobronchial US- or bronchofibroscopy-guided biopsies (n = 66), pleural fluid analysis (n = 47), other solid organ biopsies (n = 43), US-guided axillary or supraclavicular lymph node biopsies (n = 31), and cerebrospinal fluid analysis (n = 12). CT findings at the initial diagnosis and rebiopsy were analyzed. Progression-free survival, the duration from the start of TKI therapy to rebiopsy, and survival were calculated. Results At rebiopsy, 144 (47.4%) patients were T790M mutation positive. The percentages of T790M mutation-positive NSCLCs were similar in 106 patients with rebiopsy of the lungs (53 [50%] of 106) and in 77 patients with rebiopsy of the primary lung lesions (36 [47%] of 77). T790M mutation positivity was associated with peripheral tumors (odds ratio [OR], 2.6; P = .01), pleural tag (OR, 5.0; P < .001), and air bronchogram (OR, 4.0; P = .006) at CT after TKI failure. The duration from the start of TKI therapy to rebiopsy was longer in T790M mutation-positive than in T790M mutation-negative patients (20.5 vs 13.6 months; P < .001). Cumulative survival from the time of rebiopsy to the last follow-up was significantly longer in patients with T790M mutation-positive lung cancers (P = .014). However, median survival time after rebiopsy was not statistically different between patients with and those without T790M mutation. Conclusion Peripheral tumor location with vascular convergence, the presence of a pleural tag, and air bronchogram of lung lesions at CT at the time of rebiopsy were significantly associated with T790M mutation in patients with non-small cell lung cancer after first-line epidermal growth factor receptor-tyrosine kinase inhibitor therapy failure. © RSNA, 2018 Online supplemental material is available for this article.

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Year:  2018        PMID: 30015588     DOI: 10.1148/radiol.2018180070

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  7 in total

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2.  Frequency and clinical features of BRAF mutations among patients with stage III/IV lung adenocarcinoma without EGFR/ALK aberrations.

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4.  Analysis of the Diagnosis Model of Peripheral Non-Small-Cell Lung Cancer under Computed Tomography Images.

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Review 5.  Radiogenomics in Interventional Oncology.

Authors:  Amgad M Moussa; Etay Ziv
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6.  Diffuse Lung Metastases in EGFR-Mutant Non-Small Cell Lung Cancer.

Authors:  Subba R Digumarthy; Dexter P Mendoza; Atul Padole; Tianqi Chen; P Gabriel Peterson; Zofia Piotrowska; Lecia V Sequist
Journal:  Cancers (Basel)       Date:  2019-09-13       Impact factor: 6.639

7.  A CT-derived deep neural network predicts for programmed death ligand-1 expression status in advanced lung adenocarcinomas.

Authors:  Ying Zhu; Yang-Li Liu; Yu Feng; Xiao-Yu Yang; Jing Zhang; Dan-Dan Chang; Xi Wu; Xi Tian; Ke-Jing Tang; Can-Mao Xie; Yu-Biao Guo; Shi-Ting Feng; Zun-Fu Ke
Journal:  Ann Transl Med       Date:  2020-08
  7 in total

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