When cancer and heart failure cross paths: a case report of severe cardiorenal compromise associated with the anti-CD20 monoclonal antibody rituximab in a patient with dilated cardiomyopathy.

L. Nikolaidis
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引用次数: 10

Abstract

The authors describe the case of a 41-year-old man with end-stage, nonischemic dilated cardiomyopathy of 11 years' duration. The patient had been deemed ineligible for transplantation, despite his young age, when he was diagnosed with non-Hodgkin's lymphoma 7 years previously. Since he had survived the lymphoma without significant chemotherapy, while his cardiovascular and renal status continued to deteriorate, the issue was revisited. In an attempt to at least render him eligible for an assist device, a novel, promising, and reportedly nontoxic immunomodulation therapy for his lymphoma was employed. This consisted of infusion of the monoclonal antibody rituximab, specifically targeting the CD20 antigen on B cells. Despite testimonials concerning the benign nature of the treatment, the patient was unable to tolerate it and his clinical condition deteriorated rapidly, eventually leading to his death. The authors discuss potential mechanisms that might have accounted for the patient's cardiorenal compromise, with a focus on a very rare "cytokine release" syndrome attributed to this type of monoclonal antibody therapy and the probable interplay of cytokines in advanced heart failure. (c)2001 CHF, Inc.
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当癌症和心力衰竭交叉路径:扩张型心肌病患者中抗cd20单克隆抗体利妥昔单抗相关的严重心肾损害病例报告
作者描述了一个41岁的终末期,非缺血性扩张型心肌病持续11年的病例。7年前,当患者被诊断为非霍奇金淋巴瘤时,尽管他很年轻,但他被认为不适合移植。由于他在淋巴瘤中幸存下来,没有进行重大化疗,而他的心血管和肾脏状况继续恶化,这个问题被重新审视。为了至少使他有资格获得辅助装置,我们采用了一种新颖的、有前途的、据报道无毒的免疫调节疗法来治疗他的淋巴瘤。这包括输注单克隆抗体利妥昔单抗,特异性靶向B细胞上的CD20抗原。尽管证词表明这种治疗是良性的,但病人无法忍受,他的临床状况迅速恶化,最终导致他死亡。作者讨论了可能导致患者心肾损害的潜在机制,重点关注了由这种类型的单克隆抗体治疗引起的非常罕见的“细胞因子释放”综合征,以及细胞因子在晚期心力衰竭中的可能相互作用。(c)2001 CHF, Inc。
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