Masucci Chiara, Pepe Sara, La Rocca Ursula, Zullino Veronica, De Propris Maria Stefania, Barberi Walter, Iori Anna Paola, Martelli Sabina, Ruberto Franco, Martelli Maurizio, Di Rocco Alice
Division of Hematology, Department of Translational and Precision Medicine, Sapienza University, Rome, Italy.
National Blood Centre, Italian National Institute of Health, Rome, Italy.
Front Oncol. 2023 Jun 15;13:1171031. doi: 10.3389/fonc.2023.1171031. eCollection 2023.
Anti-CD19 chimeric antigen receptor (CAR) T cell therapy actually represents the standard of care for multiple relapsed or refractory primary mediastinal B-cell lymphoma (r/r PMBCL). Checkpoint inhibitors, such as pembrolizumab, appear to be a safe and effective treatment strategy for patients who are ineligible for or resistant to autologous stem cell transplantation. Although preclinical studies suggested that checkpoint inhibitors may enhance the vitality and anti-tumor activity of CAR T cells, there are no substantial/robust clinical data about the immune-mediated toxicity of their association. We describe a case of a severe cutaneous adverse event arising immediately after Cytokine Release Syndrome (CRS) on day +6 from CAR T cells infusion in a young r/r PMBCL patient who previously received pembrolizumab. These skin lesions were interpreted as an immune mediated adverse event, considering their prompt improvement and fully recovering achieved with the addition of immunoglobulin infusion to systemic steroid therapy. This case of life-threatening cutaneous adverse event calls for further investigations about off-target immune-related adverse events deriving from the combination of CAR T cell therapy and checkpoint inhibition, whose synergic therapeutic effect is promising.
抗CD19嵌合抗原受体(CAR)T细胞疗法实际上代表了多次复发或难治性原发性纵隔B细胞淋巴瘤(r/r PMBCL)的治疗标准。检查点抑制剂,如帕博利珠单抗,对于不符合自体干细胞移植条件或对其耐药的患者似乎是一种安全有效的治疗策略。尽管临床前研究表明检查点抑制剂可能增强CAR T细胞的活力和抗肿瘤活性,但关于它们联合使用的免疫介导毒性,尚无大量有力的临床数据。我们描述了一例年轻的r/r PMBCL患者,在接受CAR T细胞输注后第6天发生细胞因子释放综合征(CRS)后立即出现严重皮肤不良事件,该患者之前接受过帕博利珠单抗治疗。考虑到通过在全身类固醇治疗基础上加用免疫球蛋白输注后这些皮肤病变迅速改善并完全恢复,这些皮肤病变被解释为免疫介导的不良事件。这例危及生命的皮肤不良事件需要进一步研究CAR T细胞疗法与检查点抑制联合使用产生的脱靶免疫相关不良事件,其协同治疗效果很有前景。