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Non-Small Cell Lung Cancer with Resistance to EGFR-TKI Therapy: CT Characteristics of T790M Mutation-positive Cancer
被引:23
|作者:
Koo, Hyun Jung
[1
,2
]
Kim, Mi Young
[1
,2
]
Park, Sojung
[3
,6
]
Lee, Han Na
[7
]
Kim, Hwa Jung
[4
]
Lee, Jae Cheol
[5
]
Kim, Sang-We
[5
]
Lee, Dae Ho
[5
]
Choi, Chang-Min
[3
,5
]
机构:
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol, Olymp Ro 43 Gil 88, Seoul 05505, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Res Inst Radiol, Olymp Ro 43 Gil 88, Seoul 05505, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pulm & Crit Care Med, Olymp Ro 43 Gil 88, Seoul 05505, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Olymp Ro 43 Gil 88, Seoul 05505, South Korea
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Olymp Ro 43 Gil 88, Seoul 05505, South Korea
[6] Hallym Univ, Dongtan Sacred Heart Hosp, Dept Pulm & Crit Care Med, Dongtan, South Korea
[7] Kyung Hee Univ, Kyung Hee Univ Hosp Gangdong, Coll Med, Dept Radiol, Seoul, South Korea
来源:
关键词:
RESPONSE EVALUATION CRITERIA;
TYROSINE KINASE INHIBITORS;
ACQUIRED-RESISTANCE;
GEFITINIB RESISTANCE;
HISTOLOGIC-SUBTYPES;
1ST-LINE TREATMENT;
OPEN-LABEL;
GROWTH;
ADENOCARCINOMA;
CHEMOTHERAPY;
D O I:
10.1148/radiol.2018180070
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
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. (c) RSNA, 2018
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页码:227 / 237
页数:11
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