Zheng Jian, Zhou Nan, Pang Dexiang
Oncology Department, The Second Affiliated Hospital of Zhejiang Chinese Medicine University, Hangzhou, Zhejiang, China.
Oncology Department, The Traditional Chinese Medicine Hospital of Linping District, Hangzhou, Zhejiang, China.
Front Oncol. 2025 Aug 7;15:1561440. doi: 10.3389/fonc.2025.1561440. eCollection 2025.
Nintedanib, a small molecule multi-target tyrosine kinase inhibitor, can block the fibrosis process and slow disease progression. Acute thrombocytopenia and fibrinogen reduction caused by nintedanib is a rare clinical event, with few studies reported.
We report the case of an 89-year-old male diagnosed with advanced renal cell carcinoma who developed immune-related interstitial lung disease after treatment with sintilimab injection combined with axitinib. After prescribed nintedanib treatment, the patient's platelet count decreased from 241×10 μ g/L to 49×10 μ g/L and fibrinogen decreased from 5.61 g/L to 0.76 g/L. Based on the patient's medical history, laboratory test results, and examination results, the diagnosis was made that it was nintedanib-induced reduction in platelet and fibrinogen levels. After discontinuation of nintedanib, the patient's platelets and fibrinogen returned to normal, and no further reduction in platelets and fibrinogen was observed during the follow-up period. This case report suggests to physicians that if there is an unexplained decrease in platelet and fibrinogen levels during nintedanib treatment, nintedanib-induced factors should be considered.
Thrombocytopenia and fibrinogens abnormal are rare but serious adverse effect of nintedanib. This case highlights the importance of early recognition and monitoring of platelet counts and coagulation function in patients receiving nintedanib. Suspect drug discontinuation and active supportive care are essential. Further research is needed to elucidate the underlying mechanisms and then make corresponding treatment recommendations.
尼达尼布是一种小分子多靶点酪氨酸激酶抑制剂,可阻断纤维化进程并减缓疾病进展。尼达尼布引起的急性血小板减少和纤维蛋白原降低是一种罕见的临床事件,鲜有研究报道。
我们报告一例89岁男性患者,诊断为晚期肾细胞癌,在接受信迪利单抗注射液联合阿昔替尼治疗后发生免疫相关间质性肺病。在给予尼达尼布治疗后,患者的血小板计数从241×10⁹/L降至49×10⁹/L,纤维蛋白原从5.61g/L降至0.76g/L。根据患者病史、实验室检查结果和检查结果,诊断为尼达尼布引起的血小板和纤维蛋白原水平降低。停用尼达尼布后,患者的血小板和纤维蛋白原恢复正常,随访期间未观察到血小板和纤维蛋白原进一步降低。该病例报告提示医生,在尼达尼布治疗期间,如果出现无法解释的血小板和纤维蛋白原水平降低,应考虑尼达尼布诱导的因素。
血小板减少和纤维蛋白原异常是尼达尼布罕见但严重的不良反应。本病例强调了在接受尼达尼布治疗的患者中早期识别和监测血小板计数及凝血功能的重要性。怀疑药物停用并给予积极的支持治疗至关重要。需要进一步研究以阐明潜在机制,进而提出相应的治疗建议。