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
相关论文
共 29 条
  • [1] Predictive factors for interstitial lung disease, antitumor response, and survival in non-small-cell lung cancer patients treated with gefitinib
    Ando, M
    Okamoto, I
    Yamamoto, N
    Takeda, K
    Tamura, K
    Seto, T
    Ariyoshi, Y
    Fukuoka, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (16) : 2549 - 2556
  • [2] Radiation recall:: A well recognized but neglected phenomenon
    Azria, D
    Magné, N
    Zouhair, A
    Castadot, P
    Culine, S
    Ychou, M
    Stupp, R
    Van Houtte, P
    Dubois, JB
    Ozsahin, M
    [J]. CANCER TREATMENT REVIEWS, 2005, 31 (07) : 555 - 570
  • [3] Radiation Recall with Anticancer Agents
    Burris, Howard A., III
    Hurtig, Jane
    [J]. ONCOLOGIST, 2010, 15 (11) : 1227 - 1237
  • [4] Gefitinib-Related Interstitial Lung Disease in Taiwanese Patients With Non-Small-Cell Lung Cancer
    Chang, Shih-Chieh
    Chang, Cheng-Yu
    Chang, Shu-Ju
    Yuan, Mei-Kang
    Lai, Yi-Chun
    Liu, Yu-Chang
    Chen, Cheng-Yu
    Kuo, Li-Chiao
    Yu, Chong-Jen
    [J]. CLINICAL LUNG CANCER, 2013, 14 (01) : 55 - 61
  • [5] Update of epidermal growth factor receptor-tyrosine kinase inhibitors in non-small-cell lung cancer
    Chen, Yuh-Min
    [J]. JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2013, 76 (05) : 249 - 257
  • [6] Mechanisms of enhanced radiation response following epidermal growth factor receptor signaling inhibition by Erlotinib (Tarceva)
    Chinnaiyan, P
    Huang, SM
    Vallabhaneni, G
    Armstrong, E
    Varambally, S
    Tomlins, SA
    Chinnaiyan, AM
    Harari, PM
    [J]. CANCER RESEARCH, 2005, 65 (08) : 3328 - 3335
  • [7] Radiation recall pneumonitis induced by chemotherapy after thoracic radiotherapy for lung cancer
    Ding, Xiao
    Ji, Wei
    Li, Junling
    Zhang, Xiangru
    Wang, Luhua
    [J]. RADIATION ONCOLOGY, 2011, 6
  • [8] Non Small Cell Lung Cancer
    Ettinger, David S.
    Akerley, Wallace
    Bepler, Gerold
    Blum, Matthew G.
    Chang, Andrew
    Cheney, Richard T.
    Chirieac, Lucian R.
    D'Amico, Thomas A.
    Demmy, Todd L.
    Ganti, Apar Kishor P.
    Govindan, Ramaswamy
    Grannis, Frederic W., Jr.
    Jahan, Thierry
    Jahanzeb, Mohammad
    Johnson, David H.
    Kessinger, Anne
    Komaki, Ritsuko
    Kong, Feng-Ming
    Kris, Mark G.
    Krug, Lee M.
    Le, Quynh-Thu
    Lennes, Inga T.
    Martins, Renato
    O'Malley, Janis
    Osarogiagbon, Raymond U.
    Otterson, Gregory A.
    Patel, Jyoti D.
    Pisters, Katherine M.
    Reckamp, Karen
    Riely, Gregory J.
    Rohren, Eric
    Simon, George R.
    Swanson, Scott J.
    Wood, Douglas E.
    Yang, Stephen C.
    [J]. JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2010, 8 (07): : 740 - +
  • [9] Interstitial lung disease in Japanese patients with non-small cell lung cancer receiving gefitinib: An analysis of risk factors and treatment outcomes in Okayama lung cancer study group
    Hotta, K
    Kiura, K
    Tabata, M
    Harita, S
    Gemba, K
    Yonei, T
    Bessho, A
    Maeda, T
    Moritaka, T
    Shibayama, T
    Matsuo, K
    Kato, K
    Kanehiro, A
    Tanimoto, Y
    Matsuo, K
    Ueoka, H
    Tanimoto, M
    [J]. CANCER JOURNAL, 2005, 11 (05) : 417 - 424
  • [10] Comparison of the Incidence and Pattern of Interstitial Lung Disease During Erlotinib and Gefitinib Treatment in Japanese Patients with Non-small Cell Lung Cancer The Okayama Lung Cancer Study Group Experience
    Hotta, Katsuyuki
    Kiura, Katsuyuki
    Takigawa, Nagio
    Yoshioka, Hiroshige
    Harita, Shingo
    Kuyama, Shoichi
    Yonei, Toshiro
    Fujiwara, Keiichi
    Maeda, Tadashi
    Aoe, Keisuke
    Ueoka, Hiroshi
    Kamei, Haruhito
    Umemura, Shigeki
    Moritaka, Tomonori
    Segawa, Yoshihiko
    Kawai, Haruyuki
    Bessho, Akihiro
    Kato, Katsuya
    Tabata, Masahiro
    Tanimoto, Mitsune
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (02) : 179 - 184