Division of Respirology, NTT Medical Center Tokyo, 5-9-22 Higashigotanda Shinagawa, Tokyo 141-0022, Japan.
Jpn J Clin Oncol. 2011 Apr;41(4):498-502. doi: 10.1093/jjco/hyr006. Epub 2011 Feb 7.
Interstitial lung disease in patients with colorectal cancer during chemotherapy combined with bevacizumab is rare.
We reviewed 104 colorectal cancer patients treated with standard chemotherapy with bevacizumab and examined the incidence of interstitial lung disease and its clinical features.
We identified interstitial lung disease in four patients (3.85%). All patients were male. The median age was 64.5 years. Three of four patients had a history of smoking; median smoking index was 40 pack-years. Except one patient who had asymptomatic pulmonary fibrosis, chest computed tomography before chemotherapy showed no fibrotic changes. Pulmonary function test before chemotherapy showed normal values. All patients had received median 10 cycles (range 10-15 cycles) of FOLFOX before the onset of interstitial lung disease. Interstitial lung disease developed during FOLFOX + bevacizumab in two patients and during FOLFIRI + bevacizumab in two patients. The initial symptom of interstitial lung disease was fever in all patients. The median duration from the last chemotherapy to the onset of interstitial lung disease was 3.5 days (range 2-8 days). Three of four patients showed Grade 3 or more severity of interstitial lung disease according to Common Terminology Criteria for Adverse Events v3.0. High-dose steroid therapy was effective in all patients.
Interstitial lung disease induced by standard chemotherapy with bevacizumab is rare, but rapidly progressed and were severe in our experience.
结直肠癌患者在化疗联合贝伐珠单抗治疗期间发生间质性肺病较为罕见。
我们回顾了 104 例接受标准化疗联合贝伐珠单抗治疗的结直肠癌患者,检查了间质性肺病的发生率及其临床特征。
我们发现了 4 例(3.85%)间质性肺病患者。所有患者均为男性,中位年龄为 64.5 岁。4 例中有 3 例有吸烟史,中位吸烟指数为 40 包年。除了 1 例无症状性肺纤维化患者外,化疗前胸部计算机断层扫描未显示纤维化改变。化疗前肺功能检查显示正常。所有患者在间质性肺病发作前均接受了中位数为 10 个周期(范围 10-15 个周期)的 FOLFOX 治疗。2 例患者在 FOLFOX+贝伐珠单抗治疗期间,2 例患者在 FOLFIRI+贝伐珠单抗治疗期间发生间质性肺病。所有患者的间质性肺病初始症状均为发热。从最后一次化疗到间质性肺病发作的中位时间为 3.5 天(范围 2-8 天)。根据不良事件通用术语标准 v3.0,4 例中有 3 例患者的间质性肺病严重程度达到 3 级或更高级别。所有患者均接受了大剂量类固醇治疗,效果良好。
在我们的经验中,标准化疗联合贝伐珠单抗引起的间质性肺病罕见,但进展迅速且严重。