Interstitial Lung Disease in Japanese Patients with Lung Cancer

Shoji Kudoh(Nippon Medical School), Harubumi Kato(Tokyo Medical University Hospital), Yutaka Nishiwaki(National Cancer Center Hospital East), Masahiro Fukuoka(Kindai University), Kouichiro Nakata, Yukito Ichinose(National Hospital Organization Kyushu Cancer Center), Masahiro Tsuboi(Tokyo Medical University Hospital), Soichiro Yokota(Toneyama National Hospital), Kazuhiko Nakagawa(Kindai University), Moritaka Suga(Saiseikai Kumamoto Hospital), Haiyi Jiang(AstraZeneca (Japan)), Y. Itoh(AstraZeneca (Japan)), Alison Armour(AstraZeneca (United Kingdom)), Claire Watkins(AstraZeneca (United Kingdom)), Tim Higenbottam(AstraZeneca (United Kingdom)), Fredrik Nyberg(Karolinska Institutet)
American Journal of Respiratory and Critical Care Medicine
March 12, 2008
Cited by 488

Abstract

RATIONALE: Interstitial lung disease (ILD) occurs in Japanese patients with non-small cell lung cancer (NSCLC) receiving gefitinib. OBJECTIVES: To elucidate risk factors for ILD in Japanese patients with NSCLC during treatment with gefitinib or chemotherapy. METHODS: In a prospective epidemiologic cohort, 3,166 Japanese patients with advanced/recurrent NSCLC were followed for 12 weeks on 250 mg gefitinib (n = 1,872 treatment periods) or chemotherapy (n = 2,551). Patients who developed acute ILD (n = 122) and randomly selected control subjects (n = 574) entered a case-control study. Adjusted incidence rate ratios were estimated from case-control data by odds ratios (ORs) with 95% confidence intervals (CIs) using logistic regression. Crude (observed) incidence rates and risks were calculated from cohort data. MEASUREMENTS AND MAIN RESULTS: The observed (unadjusted) incidence rate over 12 weeks was 2.8 (95% CI, 2.3-3.3) per 1,000 person-weeks, 4.5 (3.5-5.4) for gefitinib versus 1.7 (1.2-2.2) for chemotherapy; the corresponding observed naive cumulative incidence rates at the end of 12-week follow-up were 4.0% (3.0-5.1%) and 2.1% (1.5-2.9%), respectively. Adjusted for imbalances in risk factors between treatments, the overall OR for gefitinib versus chemotherapy was 3.2 (1.9-5.4), elevated chiefly during the first 4 weeks (3.8 [1.9-7.7]). Other ILD risk factors in both groups included the following: older age, poor World Health Organization performance status, smoking, recent NSCLC diagnosis, reduced normal lung on computed tomography scan, preexisting chronic ILD, concurrent cardiac disease. ILD-related deaths in patients with ILD were 31.6% (gefitinib) versus 27.9% (chemotherapy); adjusted OR, 1.05 (95% CI, 0.3-3.2). CONCLUSIONS: ILD was relatively common in these Japanese patients with NSCLC during therapy with gefitinib or chemotherapy, being higher in the older, smoking patient with preexisting ILD or poor performance status. The risk of developing ILD was higher with gefitinib than chemotherapy, mainly in the first 4 weeks.


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