A case of life threatening acute Nivolumab induced autoimmune haemolytic anaemia

A. Farooq, C. Keohane, Maeve P. Crowley, Laura Whelan, Neasa Gallwey, C. Brady, S. O'Reilly
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Abstract

Autoimmune haemolytic anemia is a rare but potentially catastrophic adverse event of im-mune checkpoint inhibitor therapy. We present the case of a gentleman who presented with non-specific symptoms while undergoing adjuvant Nivolumab therapy after potential-ly curative surgery for gastroesophageal cancer. The patient’s haemoglobin deteriorated to 4.7 g/dl with no evidence of bleeding and serologic tests indicative of hemolysis. He re-ceived emergent massive RCC transfusion receiving 9 units of bloods in 1 night, and was commenced on high dose methylprednisolone. During subsequent weeks of inpatient care, the patient continued to received multiple daily red cell transfusions and had a total of 53 RCC transfusions during admission, along with high doses of steroids,4 doses of weekly Rituximab as well as 2 doses of IVIG.While he was discharged on day 38 of admission, he required a slow taper of steroids over 6 months. Immune related hemolytic anemias are a rare corollary of immune check point inhibitors. The cases of immune related AIHA docu-mented in the literature were treated with steroids, Rituximab and IVIG, which are also rec-ommended by guidelines for the treatment of immune related haemolytic anemias.
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危及生命的急性纳武单抗诱导自身免疫性溶血性贫血1例
自身免疫性溶血性贫血是免疫检查点抑制剂治疗的罕见但潜在的灾难性不良事件。我们提出的情况下,一位先生谁提出了非特异性症状,而接受辅助尼武单抗治疗后,潜在的治愈手术胃食管癌。患者血红蛋白恶化至4.7 g/dl,无出血迹象,血清学检查提示溶血。患者接受紧急大量肾细胞癌输血,1晚输9单位血,并开始大剂量甲基强的松龙治疗。在随后几周的住院治疗中,患者继续接受每日多次红细胞输注,入院期间共接受53次RCC输注,同时给予高剂量类固醇、每周4剂利妥昔单抗和2剂IVIG。当他在入院第38天出院时,他需要在6个月内逐渐减少类固醇的使用。免疫相关溶血性贫血是免疫检查点抑制剂的罕见结果。文献中记录的免疫相关AIHA病例用类固醇、利妥昔单抗和IVIG治疗,这些治疗指南也推荐用于免疫相关溶血性贫血的治疗。
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