首页> 美国卫生研究院文献>Journal of Thoracic Disease >A case of tuberculosis reactivation suspected of cancer progression during oral tyrosine kinase inhibitor treatment in a patient diagnosed as non-small cell lung cancer
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A case of tuberculosis reactivation suspected of cancer progression during oral tyrosine kinase inhibitor treatment in a patient diagnosed as non-small cell lung cancer

机译:疑似非小细胞肺癌患者口服酪氨酸激酶抑制剂治疗期间结核再活化疑似发展的一例病例

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摘要

We report a first case of a patient experiencing reactivation of pulmonary tuberculosis (TB) during treatment of oral tyrosine kinase inhibitor (TKI) with non-small cell lung cancer (NSCLC). A 44-year-old male patient visited the hospital with cough. He had been treated with erlotinib (oral TKI) for 8 months after being diagnosed as NSCLC with sensitive epidermal growth factor receptor mutation in our clinic. At initial chest imaging, the patient had fibroatelectatic calcified granuloma in the right upper lobe (RUL) apex as well as 1.9 cm × 2.5 cm sized cancer mass encasing the RUL bronchus. He had not been treated for active pulmonary TB before. He had no known history of contact with active TB patients. During the past treatment period, he had shown overall stable response to erlotinib for 8 months. However, chest computed tomography taken for the fourth response evaluation showed increased number and size of nodules with bronchial luminal narrowing in RUL compared to the last exam, suggesting disease progression. We performed bronchoscopy to re-biopsy the cancer mass. Mucosal biopsy and bronchial washing fluid culture revealed active endobronchial pulmonary TB rather than lung cancer progression. Based on these study results, we started anti-TB medications without changing chemotherapy regimen. After 7 months of treatment for pulmonary TB with erlotinib maintenance, he has been shown successful regression of pulmonary TB with stable chemotherapeutic response. Previously, several reports have described the effect of anti-cancer therapy on the treatment of active TB. However, there has been no case report presenting TB reactivation during oral TKI treatment in NSCLC. Therefore, we suggest that the risk of TB reactivation should be considered in patients with solid organ malignancies even if targeted agents are used. Moreover, misdiagnosis of disease progression must be ruled out.
机译:我们报告的第一例患者在治疗非小细胞肺癌(NSCLC)的口服酪氨酸激酶抑制剂(TKI)期间发生肺结核(TB)的重新激活。一名44岁的男性患者咳嗽前往医院。在我们诊所被诊断为具有敏感表皮生长因子受体突变的NSCLC后,他已经接受了厄洛替尼(口服TKI)治疗8个月。在最初的胸部影像学检查中,患者右上叶(RUL)尖部有纤维化钙化肉芽肿,并有1.9厘米×2.5厘米大小的癌块包住RUL支气管。他之前没有接受过活动性肺结核的治疗。他没有与活动性结核病患者接触的历史。在过去的治疗期间,他对厄洛替尼的总体稳定反应持续了8个月。然而,用于第四次反应评估的胸部计算机断层扫描显示,与上次检查相比,RUL中结节的数量和大小增加,支气管腔狭窄。我们进行了支气管镜检查以对癌块进行再次活检。粘膜活检和支气管冲洗液培养显示活跃的支气管内肺结核,而不是肺癌进展。基于这些研究结果,我们在不改变化疗方案的情况下开始了抗结核药物治疗。厄洛替尼维持治疗肺结核7个月后,他被证明可以成功退回肺结核,并具有稳定的化疗反应。以前,有几篇报道描述了抗癌疗法对活动性结核病的治疗作用。但是,尚无病例报告在NSCLC口服TKI治疗期间出现结核再活化。因此,我们建议即使使用靶向药物,实体器官恶性肿瘤患者也应考虑结核再激活的风险。此外,必须排除对疾病进展的误诊。

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