Outcomes of research biopsies in clinical trials of EGFR mutation-positive non-small cell lung cancer patients pretreated with EGFR-tyrosine kinase inhibitors

被引:9
作者
Liao, Bin-Chi [1 ,6 ,9 ]
Bai, Ya-Ying [1 ]
Lee, Jih-Hsiang [1 ,3 ]
Lin, Chia-Chi [1 ,7 ]
Lin, Shu-Yung [2 ,5 ]
Lee, Yee-Fan [4 ]
Ho, Chao-Chi [2 ]
Shih, Jin-Yuan [2 ]
Chang, Yeun-Chung [4 ]
Yu, Chong-Jen [2 ]
Yang, James Chih-Hsin [1 ,8 ,9 ]
Yang, Pan-Chyr [2 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Med Res, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Med Imaging, 7 Chung Shan South Rd, Taipei 100, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Internal Med, Jinshan Branch, New Taipei, Taiwan
[6] Natl Taiwan Univ, Coll Med, Natl Taiwan Univ Canc Ctr, Taipei, Taiwan
[7] Natl Taiwan Univ, Dept Urol, Coll Med, Taipei, Taiwan
[8] Natl Taiwan Univ, Grad Inst Oncol, Coll Med, Taipei, Taiwan
[9] Natl Taiwan Univ, Grad Inst Clin Med, Coll Med, Taipei, Taiwan
关键词
Complications; Computed tomography-guided percutaneous core needle biopsy; EGFR mutation; Non-small cell lung cancer; Research biopsies; ACQUIRED-RESISTANCE; PULMONARY-LESIONS; PHASE-III; ACTIVATING MUTATIONS; IMPRINT CYTOLOGY; CORE BIOPSY; ADENOCARCINOMA; GEFITINIB; AFATINIB; CHEMOTHERAPY;
D O I
10.1016/j.jfma.2017.04.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/purpose: Research biopsies (RBs) are crucial for developing novel molecular targeted agents. However, the safety and diagnostic yields of RBs have not been investigated in EGFR mutation-positive non-small cell lung cancer (NSCLC) patients pretreated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). Methods: We searched the medical records of NSCLC patients who participated in lung cancer clinical trials and underwent mandatory RBs between 2012 and 2014 at our institution. Only patients with EGFR mutation-positive NSCLC pretreated with at least 1 EGFR-TKI were enrolled. Results: Of 140 enrolled patients, 73 (52.1%) and 59 (42.1%) had exon 19 deletions and exon 21 L858R mutation, respectively. Before RBs, 108 (77.1%), 83 (59.3%), and 36 (25.7%) patients had been treated with gefitinib, erlotinib, and afatinib, respectively. Computed tomography-guided percutaneous core needle biopsy was the most frequently used modality among 181 RBs performed (50.8%), followed by ultrasonography-guided (32.0%) and endoscopic RBs (16.0%). The most common RB sites were the lung (69.6%), pleura (8.8%), and liver (6.1%). Pathologic examinations revealed malignant cells in most RB specimens (72.9%). Complications due to RBs included pneumothorax (11.6%), bleeding (6.1%), and infection (1.1%). Only 1 patient required chest tube placement for pneumothorax, and 2 patients underwent endotracheal intubation because of bleeding. Conclusion: RBs in this patient population were generally safe. Pneumothorax was the most frequent complication; bleeding, while infrequent, increased the risk of severe events. The diagnostic yields and complications of any particular modality should therefore be discussed with prospective clinical trial participants. Copyright (C) 2017, Formosan Medical Association. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:326 / 331
页数:6
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