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多西他赛治疗非小细胞肺癌后引起的间质性肺炎。

Docetaxel-induced interstitial pneumonitis following non-small-cell lung cancer treatment.

作者信息

Grande C, Villanueva M J, Huidobro G, Casal J

机构信息

Servicio de Oncología Médica, Hospital Meixoeiro, Complejo Hospitalario y Universitario de Vigo, Vigo, Spain.

出版信息

Clin Transl Oncol. 2007 Sep;9(9):578-81. doi: 10.1007/s12094-007-0106-4.

Abstract

Interstitial pneumonitis has been described infrequently following administration of docetaxel, used alone or in combination with other chemotherapeutic agents or concurrent irradiation, for non-small-cell lung cancer (NSCLC). This toxicity is of special relevance in NSCLC, as clinical severity and differential diagnosis may be especially challenging. It seems to be due to type I and type IV hypersensitivity reactions to the drug. Clinical and radiographic features are nonspecific and diagnosis is made by exclusion. The rate of grade III-IV docetaxel-induced pneumonitis, ranging from 7 to 47%, depends on several factors, including total dose, chemotherapy schedule and especially concomitant docetaxel treatment with gemcitabine and radiotherapy. Although the usual outcome is cure, it sometimes eventually progresses to pulmonary fibrosis despite steroid treatment. This toxicity must be taken into account when planning treatment strategies for NSCLC in order to reduce its rate and to achieve prompt diagnosis and treatment.

摘要

在单独使用或与其他化疗药物联合使用多西他赛或同时进行放疗治疗非小细胞肺癌(NSCLC)后,间质性肺炎的报道较少。这种毒性在NSCLC中具有特殊意义,因为临床严重程度和鉴别诊断可能特别具有挑战性。它似乎是由于对该药物的I型和IV型超敏反应所致。临床和影像学特征不具有特异性,诊断需排除其他疾病。III-IV级多西他赛诱导的肺炎发生率在7%至47%之间,取决于几个因素,包括总剂量、化疗方案,尤其是多西他赛与吉西他滨联合治疗以及放疗。尽管通常的结果是治愈,但有时尽管进行了类固醇治疗,最终仍会进展为肺纤维化。在制定NSCLC治疗策略时必须考虑这种毒性,以降低其发生率并实现及时诊断和治疗。

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