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  • 한국과학기술정보연구원(KISTI) 서울분원 대회의실(별관 3층)
  • 2024년 07월 03일(수) 13:30
 

Recurrent Erlotinib-Induced Interstitial Lung Disease on Non-Small Cell Lung Cancer

Tuberculosis & Respiratory Diseases / Tuberculosis & Respiratory Diseases,
2009, v.67 no.5, pp.445-448
Sang Don Park (Inha University)
Areum Kim (Inha University)
Jin-Seok Park (Inha University)
Chun Ho Shin (Inha University)
남해성 (인하대학교)
Lucia Kim (Inha University)
조재화 (인하대학교)
Jeong Sun Ryu (Inha University)
곽승민 (인하대학교)
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Abstract

Erlotinib (TarcevaⓇ) has been considered to be a new, promising oral chemotherapy agent for local advanced or metastatic non-small cell lung cancer (NSCLC). Erlotinib is regarded as relatively safe, but interstitial lung disease (ILD) related to erlotinib has been reported on an infrequent basis in Asia. We report an histologically confirmed case of recurrent erlotinib-induced ILD. Although, the patient was highly responsive to the first erlotinib treatment, the therapy was discontinued due to erlotinib-induced ILD. After intravenous high dose methylpredinisolone treatment, ILD was improved rapidly by radiologic studies, but the particular lung cancer re-emerged. We restarted the patient erlotinib on low-dose oral methylpredinisolone, resulting in a recurrence of erlotinib-induced ILD. Our case suggests that re-administration of erlotinib should be performed on a limited basis in patients that have developed ILD on previous use, even if a therapeutic effect can be estimated.

keywords
Erlotinib, Lung Diseases, Interstitial, Carcinoma, Non-Small-Cell Lung

참고문헌

1.

Johnson JR, Cohen M, Sridhara R, Chen Y, Williams GM, Duan J, et al. Approval summary for erlotinib for treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of at least one prior chemotherapy regimen. Clin Cancer Res 2005;11:6414-21.

2.

Spigel DR, Lin M, O'Neill V, Hainsworth JD. Final survival and safety results from a multicenter, open-label, phase 3b trial of erlotinib in patients with advanced nonsmall cell lung cancer. Cancer 2008;112:2749-55.

3.

Kato T, Nishio K. Clinical aspects of epidermal growth factor receptor inhibitors: benefit and risk. Respirology 2006;11:693-8.

4.

Niho S, Kubota K, Goto K, Yoh K, Ohmatsu H, Kakinuma R, et al. First-line single agent treatment with gefitinib in patients with advanced non- small-cell lung cancer: a phase II study. J Clin Oncol 2006;24:64-9.

5.

Fukui T, Mitsudomi T. Mutations in the epidermal growth factor receptor gene and effects of EGFR-tyrosine kinase inhibitors on lung cancers. Gen Thorac Cardiovasc Surg 2008;56:97-103.

6.

Liu V, White DA, Zakowski MF, Travis W, Kris MG, Ginsberg MS, et al. Pulmonary toxicity associated with erlotinib. Chest 2007;132:1042-4.

7.

Yoneda KY, Shelton DK, Beckett LA, Gandara DR. Independent review of interstitial lung disease associated with death in TRIBUTE (paclitaxel and carboplatin with or without concurrent erlotinib) in advanced non-small cell lung cancer. J Thorac Oncol 2007;2:537-43.

8.

Cohen MH, Williams GA, Sridhara R, Chen G, Pazdur R. FDA drug approval summary: gefitinib (ZD1839) (Iressa) tablets. Oncologist 2003;8:303-6.

9.

Makris D, Scherpereel A, Copin MC, Colin G, Brun L, Lafitte JJ, et al. Fatal interstitial lung disease associated with oral erlotinib therapy for lung cancer. BMC Cancer 2007;7:150.

10.

Kitajima H, Takahashi H, Harada K, Kanai A, Inomata S, Taniguchi H, et al. Gefitinib-induced interstitial lung disease showing improvement after cessation: disassociation of serum markers. Respirology 2006;11:217-20.

11.

Suzuki M, Asahina H, Konishi J, Yamazaki K, Nishimura M. Recurrent gefitinib-induced interstitial lung disease. Intern Med 2008;47:533-6.

12.

Niho S, Goto K, Yoh K, Kim YH, Ohmatsu H, Kubota K, et al. Interstitial shadow on chest CT is associated with the onset of interstitial lung disease caused by chemotherapeutic drugs. Jpn J Clin Oncol 2006;36:269-73.

Tuberculosis & Respiratory Diseases