Radiation recall pneumonitis induced by epidermal growth factor receptor-tyrosine kinase inhibitor in patients with advanced nonsmall-cell lung cancer

被引:30
作者
Chiang, Chi-Lu [1 ]
Chen, Yi-Wei [2 ,3 ]
Wu, Mei-Han [3 ,4 ]
Huang, Hsu-Ching [1 ]
Tsai, Chun-Ming [1 ,3 ]
Chiu, Chao-Hua [1 ,3 ,5 ]
机构
[1] Taipei Vet Gen Hosp, Dept Chest Med, 201,Sect 2,Shih Pai Rd, Taipei 112, Taiwan
[2] Taipei Vet Gen Hosp, Dept Oncol, Div Radiotherapy, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Dept Med, Taipei 112, Taiwan
[4] Taipei Vet Gen Hosp, Dept Radiol, Taipei 112, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Inst Clin Med, Taipei 112, Taiwan
关键词
epidermal growth factor receptor; nonsmall-cell lung cancer; radiotherapy; radiation recall pneumonitis; tyrosine kinase inhibitor; JAPANESE PATIENTS; PHASE-III; ERLOTINIB; GEFITINIB; CHEMOTHERAPY; DISEASE; RADIOTHERAPY; ADENOCARCINOMA; PREDICTION; MUTATIONS;
D O I
10.1016/j.jcma.2016.01.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Radiation recall pneumonitis (RRP) is a special form of radiation pneumonitis precipitated by certain pharmacological agents. Epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) is an effective treatment for advanced nonsmall-cell lung cancer (NSCLC) and has been reported as a potent radiation sensitizer. The incidence and general characteristics of EGFR-TKI-related RRP in patients with NSCLC remain unclear. Methods: Clinical records and serial chest images of consecutive patients with advanced NSCLC who had received thoracic radiotherapy (TRT) and EGFR-TKI treatment were retrospectively reviewed. EGFR-TKI-related RRP was diagnosed according to history, clinical manifestations, and radiographic characteristics. Potential risk factors were analyzed. Results: In total, 160 patients with NSCLC who received EGFR-TKI after TRT were identified. Of these patients, seven (4.4%) developed EGFR-TKI-related RRP. The median time interval between the end of radiotherapy and RRP was 124 days (range, 80-635 days) and that between the initiation of EGFR-TKI and RRP was 43 days (range, 18-65 days). No risk factor for the development of RRP was identified except that patients in whom EGFR-TKI was initiated within 90 days after the completion of radiotherapy had significantly higher rates of RRP than those of patients who began receiving EGFR-TKI treatment after 90 days (21% vs. 2.1%, p = 0.005). Conclusion: In patients with NSCLC who have a history of TRT, treatment with EGFR-TKI may induce not only interstitial lung disease but also RRP. Physicians should be aware of both unexpected adverse events when using EGFR-TKI. Copyright (C) 2016, the Chinese Medical Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:248 / 255
页数:8
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