Van den Eeckhaut Lisa, Hannon Heidi, Schurgers Marie, Monsaert Els, Claes Kathleen
Department of Nephrology, AZ Maria Middelares, Ghent, Belgium.
Department of Gastroenterology, AZ Maria Middelares, Ghent, Belgium.
J Gastrointest Oncol. 2022 Dec;13(6):3314-3320. doi: 10.21037/jgo-22-509.
Gemcitabine is a broadly used chemotherapeutic agent that can cause a rare but life-threatening complication called thrombotic microangiopathy (TMA). Early recognition is crucial as therapy options are limited.
We report the case of a 46-year-old patient with pancreatic adenocarcinoma who presented with severe anemia and thrombocytopenia as well as acute kidney injury. A diagnosis of gemcitabine-induced TMA was made. He became rapidly transfusion and dialysis dependent. Despite discontinuation of gemcitabine and treatment with high-dose corticotherapy as well as plasmapheresis, no improvement in both renal and hematological parameters was seen. Treatment with eculizumab was initiated. One week after the first administration, the patient no longer required packed cells nor platelet transfusions and one month later, dialysis could be discontinued. After five doses, treatment with eculizumab was stopped. Four months later, his serum creatinine was 1 mg/dL.
This case report illustrates the promising beneficial effects of eculizumab in gemcitabine-induced TMA, both regarding transfusion dependence as well as improvement in renal function, thereby allowing further therapy options in patients with an active malignancy.
吉西他滨是一种广泛使用的化疗药物,可引起一种罕见但危及生命的并发症,称为血栓性微血管病(TMA)。由于治疗选择有限,早期识别至关重要。
我们报告了一例46岁胰腺腺癌患者,该患者出现严重贫血、血小板减少以及急性肾损伤。诊断为吉西他滨诱导的TMA。他迅速变得依赖输血和透析。尽管停用了吉西他滨,并接受了大剂量皮质类固醇治疗以及血浆置换,但肾脏和血液学参数均未见改善。开始使用依库珠单抗治疗。首次给药一周后,患者不再需要输注浓缩红细胞和血小板,一个月后可以停止透析。五剂后,停止使用依库珠单抗治疗。四个月后,他的血清肌酐为1mg/dL。
本病例报告说明了依库珠单抗在吉西他滨诱导的TMA中具有有前景的有益作用,无论是在输血依赖性方面还是在肾功能改善方面,从而为患有活动性恶性肿瘤的患者提供了更多的治疗选择。