Pallotta Dante Pio, Stefanini Bernardo, Pratelli Agnese, Papayannidis Cristina, Bertuzzi Clara, Boe Maria, Girolami Francesca, Tovoli Francesco, Granito Alessandro
Unit of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedalie-ro-Universitaria di Bologna, Bologna, Italy.
Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Immunotherapy. 2025 Aug 21:1-7. doi: 10.1080/1750743X.2025.2549675.
The benefits of immune checkpoint inhibitor (ICI)-based treatment are tempered by immune-related adverse events (irAEs). However, various aspects of the pathogenesis of these events remain unclear. Here, we report the case of a 69-year-old patient with advanced hepatocellular carcinoma (HCC) developing severe anemia after 15 cycles of atezolizumab/bevacizumab. The initial workup based on bone marrow aspirate demonstrated selective deficiency of the erythroid line, CD8+ T-cell infiltrate, and Parvovirus B19 PCR (PVB19) positivity, suggesting a pure-red cell aplasia (PRCA) secondary to PVB19 infection. The patient received blood transfusion, intravenous immunoglobulin, and temporary atezolizumab/bevacizumab treatment interruption. After discharge, due to good clinical condition and stable Hb values, atezolizumab/bevacizumab therapy was resumed; however, after three cycles of re-treatment, a recurrence of anemia necessitating blood transfusions every 10 days and hyporeticulocytaemia was observed. The bone marrow aspirate was reassessed, and pure ICI-related red blood cell aplasia was suspected. Prednisone treatment (1 mg/kg per day) was initiated, resulting in progressive improvement of hemoglobin levels without the need for blood transfusion. After resolution of the anemia, treatment with atezolizumab was resumed without recurrence of anemia. This case highlights the potential for atezolizumab to be associated with hematological adverse events, possibly in conjunction with a PVB19 infection.
基于免疫检查点抑制剂(ICI)的治疗的益处因免疫相关不良事件(irAE)而受到影响。然而,这些事件发病机制的各个方面仍不清楚。在此,我们报告一例69岁晚期肝细胞癌(HCC)患者,在接受15个周期的阿替利珠单抗/贝伐单抗治疗后出现严重贫血。基于骨髓穿刺的初步检查显示红系选择性缺乏、CD8 + T细胞浸润以及细小病毒B19聚合酶链反应(PVB19)阳性,提示继发于PVB19感染的纯红细胞再生障碍(PRCA)。患者接受了输血、静脉注射免疫球蛋白,并暂时中断阿替利珠单抗/贝伐单抗治疗。出院后,由于临床状况良好且血红蛋白值稳定,恢复了阿替利珠单抗/贝伐单抗治疗;然而,在重新治疗三个周期后,观察到贫血复发,需要每10天输血一次,且网织红细胞减少。对骨髓穿刺进行了重新评估,怀疑是单纯的ICI相关红细胞再生障碍。开始使用泼尼松治疗(每天1mg/kg),血红蛋白水平逐渐改善,无需输血。贫血缓解后,恢复阿替利珠单抗治疗,未再出现贫血复发。该病例突出了阿替利珠单抗可能与血液学不良事件相关的可能性,可能与PVB19感染有关。