Genestreti Giovenzio, Di Battista Monica, Trisolini Rocco, Denicolò Fabio, Valli Mirca, Lazzari-Agli Luigi Arcangelo, Dalpiaz Giorgia, De Biase Dario, Bartolotti Marco, Cavallo Giovanna, Brandes Alba A
1 Department of Clinical Oncology, AUSL Bologna, Bologna - Italy.
Tumori. 2015 Jun 25;101(3):e92-5. doi: 10.5301/tj.5000275.
Pulmonary toxicity is a well-known complication observed with several anticancer drugs. Docetaxel, a taxane chemotherapy drug widely used in the treatment of many types of solid tumors including non-small cell lung cancer (NSCLC), rarely causes infiltrative pneumonitis. The exact mechanism by which docetaxel develops this side effect is not well understood; probably it is produced by type I and IV hypersensitivity responses. Here we describe 2 cases of infiltrative pneumonitis induced by docetaxel as second-line chemotherapy in advanced NSCLC.
Two patients with advanced NSCLC were treated with weekly docetaxel as second-line chemotherapy. After 3 courses of chemotherapy, restaging computed tomography (CT) of the chest revealed bilateral diffuse ground-glass opacities with a peribronchial distribution possibly indicative of hypersensitivity pneumonitis. No evidence of pulmonary embolus or pleural effusion was found. Fiberoptic bronchoscopy showed normal bronchi without lymphangitis; biopsies showed interstitial fibrosis without tumor cells. Bronchial tissue laboratory tests for fungi or bacilli were negative. No malignant cells were found at bronchoalveolar lavage. The patients were given high-dose corticosteroid therapy with prednisone 0.7 mg per kilogram per day.
After 1 month of therapy, contrast-enhanced chest CT showed complete disappearance of the pulmonary changes in both patients. Spirometry and blood gas analysis revealed complete recovery of pulmonary function. The patients continued their oncological follow-up program.
Pulmonary injury is a rare adverse event during docetaxel chemotherapy. Prompt treatment with high-dose corticosteroids is needed to avoid worsening of respiratory performance.
肺毒性是几种抗癌药物常见的并发症。多西他赛是一种紫杉烷类化疗药物,广泛用于治疗包括非小细胞肺癌(NSCLC)在内的多种实体瘤,很少引起浸润性肺炎。多西他赛产生这种副作用的确切机制尚不清楚;可能是由I型和IV型超敏反应引起的。在此,我们描述2例晚期NSCLC患者接受多西他赛二线化疗后发生浸润性肺炎的病例。
2例晚期NSCLC患者接受每周一次的多西他赛二线化疗。化疗3个疗程后,胸部重新分期计算机断层扫描(CT)显示双侧弥漫性磨玻璃影,呈支气管周围分布,可能提示过敏性肺炎。未发现肺栓塞或胸腔积液的证据。纤维支气管镜检查显示支气管正常,无淋巴管炎;活检显示间质纤维化,无肿瘤细胞。支气管组织真菌或杆菌实验室检查为阴性。支气管肺泡灌洗未发现恶性细胞。患者接受了每天每公斤0.7毫克泼尼松的大剂量糖皮质激素治疗。
治疗1个月后,增强胸部CT显示2例患者肺部病变均完全消失。肺功能测定和血气分析显示肺功能完全恢复。患者继续其肿瘤学随访计划。
多西他赛化疗期间肺损伤是一种罕见的不良事件。需要及时给予大剂量糖皮质激素治疗以避免呼吸功能恶化。