Distinctive impact of pre-existing interstitial lung disease on the risk of chemotherapy-related lung injury in patients with lung cancer

被引:13
作者
Ozawa, Yuichi [1 ]
Akahori, Daisuke [1 ]
Koda, Keigo [1 ]
Abe, Takefumi [1 ]
Hasegawa, Hirotsugu [1 ]
Matsui, Takashi [1 ]
Tanahashi, Masayuki [2 ]
Niwa, Hiroshi [2 ]
Yamada, Kazunari [3 ]
Yokomura, Koshi [1 ]
Suda, Takafumi [4 ]
机构
[1] Seirei Mikatahara Gen Hosp, Dept Resp Med, Resp Dis Ctr, Kita Ku, 3453 Mikatahara, Hamamatsu, Shizuoka 4338105, Japan
[2] Seirei Mikatahara Gen Hosp, Div Thorac Surg, Resp Dis Ctr, Kita Ku, 3453 Mikatahara, Hamamatsu, Shizuoka 4338105, Japan
[3] Seirei Mikatahara Gen Hosp, Dept Radiat Oncol, Kita Ku, 3453 Mikatahara, Hamamatsu, Shizuoka 4338105, Japan
[4] Hamamatsu Univ Sch Med, Dept Internal Med, Div 2, Higashi Ku, 1-20-1 Handayama, Hamamatsu, Shizuoka 4313192, Japan
关键词
Lung cancer; Interstitial lung disease; Docetaxel; S-1; IDIOPATHIC PULMONARY-FIBROSIS; PHASE-III TRIAL; ACUTE EXACERBATION; JAPANESE PATIENTS; DOCETAXEL; PNEUMONIA; S-1; CARBOPLATIN; PACLITAXEL; NIVOLUMAB;
D O I
10.1007/s00280-016-3025-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Pre-existing interstitial lung disease (pre-ILD) increases the risk of chemotherapy-related lung injury (CRLI). However, whether the risk varies by type of anti-cancer cytotoxic agent in patients with pre-ILD is unknown. In this study, we hypothesized that S-1, an oral fluoropyrimidine agent, is associated with a smaller CRLI risk than docetaxel (DTX) and investigated these agents together with radiological evaluations of pre-ILD via pre-treatment chest computed tomography (CT). Methods After reviewing 234 and 352 patients who underwent evaluable chest CT within 6 months prior to the administration of S-1 or DTX, respectively, from January 2006 to October 2014, 60 and 89, respectively, of these patients with pre-ILD were retrospectively analysed. Results In total, 2 persons administered S-1 (3 %) and 16 treated with DTX (18 %) developed CRLI (p = 0.007) after the initial treatment (mean, 61 days), of whom 1 and 7, respectively, died because of respiratory failure. Pre-treatment CT revealed that 9 S-1-treated patients (16 %) and 15 DTX-treated patients (17 %) had pre-ILD occupying more than 25 % of the lung field. Multivariate analysis demonstrated that DTX administration increased the risk of CRLI by 6.47-fold versus S-1 therapy (p = 0.016). Of note, the area occupied by pre-ILD was also associated with the risk of CRLI (< 25 %; odds ratio 0.309, p = 0.045). Conclusions Our results indicated that S-1 is associated with a smaller risk of CRLI than DTX. The area occupied by pre-ILD should also be noted when administrating anti-cancer agents.
引用
收藏
页码:1031 / 1038
页数:8
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