Bai Xueli, Cheng Jiande, Zhao Lifen, Cheng Mengyu
Department of Respiratory and Critical Care Medicine, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan, China.
Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Ann Transl Med. 2022 Jul;10(14):809. doi: 10.21037/atm-22-3233.
Numerous clinical studies have established the efficacy and safety of gefitinib for treating patients with epidermal growth factor receptor ()-mutant lung cancer. Gefitinib-induced urinary system-related adverse reactions are rare but may lead to discontinuation of gefitinib.
In our report, we describe a patient with advanced lung adenocarcinoma harboring compound G719S and S768I who developed hemorrhagic cystitis and inflammatory contracted bladder during first-line gefitinib therapy. A 56-year-old male smoker, presented with chronic cough, sputum expectoration, and shortness of breath for 6 months that had worsened over the last 2 weeks, was diagnosed with T2N2M1A stage IV adenocarcinoma of the right lower lung with bilateral lung metastases. Upon detecting a compound G719S and S768I using a next-generation sequencing-based assay, the patient was administered with gefitinib (250 mg/day) as a first-line regimen. Despite achieving partial response (PR) within 6 weeks of gefitinib therapy, the patient developed several drug-related adverse reactions, including diarrhea, elevated liver enzymes, and inflammatory contracted bladder with hemorrhagic cystitis. Routine urinalysis indicated full high-power field (HPF) view of red blood cell (RBC) and 40-50 white blood cell (WBC) counts/HPF at 1.5 months of gefitinib therapy as compared with no RBC and WBC per HPF before gefitinib therapy (normal range: 0-1 RBC/HPF and 0-3 WBC/HPF). The urinary symptoms and hematuria were alleviated after discontinuation of gefitinib. Icotinib was administered without benefit and subsequently switched to afatinib as the third-line therapy. A PR was achieved; however, it only lasted for 3 months. Then the patient was lost to follow-up.
Our case shows that gefitinib can induce hemorrhagic cystitis and contracted bladder. Clinicians must be aware that these uncommon adverse reactions affecting the urinary system could occur in patients with -mutant lung adenocarcinoma. Monitor for urinary symptoms and hematuria in this cohort of patients is essential.
众多临床研究已证实吉非替尼治疗表皮生长因子受体(EGFR)突变型肺癌患者的有效性和安全性。吉非替尼引起的泌尿系统相关不良反应罕见,但可能导致停用吉非替尼。
在我们的报告中,我们描述了一名患有复合G719S和S768I突变的晚期肺腺癌患者,在一线吉非替尼治疗期间发生了出血性膀胱炎和炎性膀胱挛缩。一名56岁男性吸烟者,出现慢性咳嗽、咳痰和气短6个月,近2周加重,被诊断为右下肺T2N2M1A期IV腺癌伴双侧肺转移。使用基于二代测序的检测方法检测到复合G719S和S768I突变后,患者接受吉非替尼(250毫克/天)作为一线治疗方案。尽管吉非替尼治疗6周内达到部分缓解(PR),但患者出现了几种药物相关不良反应,包括腹泻、肝酶升高以及伴有出血性膀胱炎的炎性膀胱挛缩。常规尿液分析显示,吉非替尼治疗1.5个月时红细胞(RBC)满高倍视野(HPF),白细胞(WBC)计数为40 - 50个/HPF,而吉非替尼治疗前RBC和WBC均无/HPF(正常范围:0 - 1个RBC/HPF和0 - 3个WBC/HPF)。停用吉非替尼后,泌尿系统症状和血尿得到缓解。给予埃克替尼治疗无效,随后改用阿法替尼作为三线治疗。再次达到PR;然而,仅持续了3个月。然后患者失访。
我们的病例表明,吉非替尼可诱发出血性膀胱炎和膀胱挛缩。临床医生必须意识到,这些影响泌尿系统的罕见不良反应可能发生在EGFR突变型肺腺癌患者中。对该队列患者监测泌尿系统症状和血尿至关重要。