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口服氟嘧啶类药物S-1诱发间质性肺病:一例报告。

An oral fluoropyrimidine agent S-1 induced interstitial lung disease: A case report.

作者信息

Yamane Hiromichi, Kinugawa Masahide, Umemura Shigeki, Shiote Yasuhiro, Kudo Kenichiro, Suwaki Toshimitsu, Kamei Haruhito, Takigawa Nagio, Kiura Katsuyuki

机构信息

Hiromichi Yamane, Masahide Kinugawa, Shigeki Umemura, Yasuhiro Shiote, Kenichiro Kudo, Toshimitsu Suwaki, Haruhito Kamei, Division of Clinical Oncology, Sumitomo-Besshi Hospital Cancer Center, 3-1 Ohji-cho, Niihama, Ehime 792-8543, Japan.

出版信息

World J Clin Oncol. 2011 Jul 10;2(7):299-302. doi: 10.5306/wjco.v2.i7.299.

Abstract

A 66-year-old Japanese man with pancreatic cancer received eleven courses of gemcitabine monotherapy. The tumor responded to gemcitabine until metastatic liver tumors progressed. Subsequently, he was treated with S-1, an oral fluoropyrimidine anticancer agent, as salvage chemotherapy. Forty-two days after initiating S-1, he presented with dyspnea and fever. Chest computed tomography showed diffuse interstitial lesions with thickening of the alveolar septa and ground glass opacity. Serum KL-6 level was elevated to 1,230 U/mL and he did not use any other drugs except insulin. Thus, the development of interstitial lung disease (ILD) was considered to be due to S-1. Arterial blood oxygen pressure was 49.6 Torr in spite of oxygen administration (5 L/min). Steroid therapy improved his symptoms and the interstitial shadows on chest radiograph. Although S-1-induced ILD has mostly been reported to be mild, clinicians should be aware that S-1 has the potential to cause fatal ILD.

摘要

一名66岁的日本胰腺癌男性患者接受了11个疗程的吉西他滨单药治疗。肿瘤对吉西他滨有反应,直到转移性肝肿瘤进展。随后,他接受了口服氟嘧啶类抗癌药S-1作为挽救性化疗。开始使用S-1 42天后,他出现呼吸困难和发热。胸部计算机断层扫描显示弥漫性间质性病变,伴有肺泡间隔增厚和磨玻璃影。血清KL-6水平升高至1230 U/mL,且除胰岛素外他未使用任何其他药物。因此,间质性肺病(ILD)的发生被认为是由S-1引起的。尽管给予了氧气(5 L/分钟),动脉血氧分压仍为49.6 Torr。类固醇治疗改善了他的症状以及胸部X光片上的间质性阴影。尽管大多数报道称S-1引起的ILD症状较轻,但临床医生应意识到S-1有导致致命性ILD的可能性。

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