Department of Hematology, Hospital Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.
Transplant Cell Ther. 2021 Sep;27(9):768.e1-768.e6. doi: 10.1016/j.jtct.2021.05.018. Epub 2021 May 30.
CD19-directed chimeric antigen receptor (CAR) T cell therapy with axicabtagene ciloleucel (axi-cel) or tisagenlecleucel (tisa-cel) is approved for the standard of care treatment of relapsed or refractory large B cell lymphoma (LBCL). Patients with LBCL involving the gastrointestinal (GI) tract are at risk of perforation after lymphoma-directed therapy. The outcomes of CAR T cell therapy in patients with GI involvement have not been reported previously. This study aimed to determine the safety and efficacy of CD19 CAR T cell therapy in patients with LBCL involvement of the GI tract. This was a single-center retrospective study of 130 consecutive patients treated with standard of care or expanded-access axi-cel or tisa-cel for LBCL. Twenty-four of these patients had radiologic involvement of the GI tract before CAR T infusion. Incidence rates of severe immune effector cell-mediated toxicities and clinical outcomes were compared between the GI involvement and non-GI involvement groups. Three of the 24 patients with GI tract involvement experienced perforation. One patient had a contained gastric perforation after leukapheresis while receiving bridging radiation therapy to the stomach. This patient was eventually able to proceed with lymphodepletion and product infusion. In the other 2 patients, GI tract perforation occurred at day +13 and day +35 after CAR T infusion. All 3 patients subsequently died while experiencing lymphoma progression. Upper GI bleeding occurred in 1 other patient in the context of progressive disease at 6 months after product infusion. The incidence rates of severe cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome, length of hospital stay, and use of anti-IL-6 and steroids were similar in the 24 patients with GI tract involvement and the 106 patients without GI tract involvement. No significant between-group differences were seen in the best overall response rate, progression-free survival, or overall survival. Our data show that outcomes of patients with GI tract involvement before CAR T cell therapy are similar to those without GI involvement, and that durable remissions can be observed. However, patients with preexisting GI tract involvement are at risk of perforation from disease progression before and after CAR T cell infusion.
CD19 导向的嵌合抗原受体(CAR)T 细胞疗法,采用 axicabtagene ciloleucel(axi-cel)或 tisagenlecleucel(tisa-cel),已被批准用于复发或难治性大 B 细胞淋巴瘤(LBCL)的标准治疗。涉及胃肠道(GI)的 LBCL 患者在接受淋巴瘤靶向治疗后有穿孔的风险。先前尚未报道过 GI 受累的 CAR T 细胞治疗患者的结果。本研究旨在确定 CD19 CAR T 细胞疗法在 GI 受累的 LBCL 患者中的安全性和疗效。这是一项对 130 例连续接受标准治疗或扩展访问 axi-cel 或 tisa-cel 治疗 LBCL 的患者进行的单中心回顾性研究。这些患者中有 24 例在 CAR T 输注前存在 GI 受累的影像学证据。比较了 GI 受累和非 GI 受累组之间严重免疫效应细胞介导的毒性发生率和临床结局。24 例 GI 受累患者中有 3 例发生穿孔。1 例患者在接受桥接胃部放射治疗的同时进行白细胞分离后发生胃穿孔,最终能够进行淋巴细胞耗竭和产品输注。另外 2 例患者在 CAR T 输注后第 13 天和第 35 天发生 GI 穿孔。所有 3 例患者随后在淋巴瘤进展时死亡。在产品输注后 6 个月,另 1 例患者因疾病进展出现上消化道出血。在 24 例 GI 受累患者和 106 例非 GI 受累患者中,严重细胞因子释放综合征和免疫效应细胞相关神经毒性综合征的发生率、住院时间、抗 IL-6 和皮质类固醇的使用情况相似。在最佳总体缓解率、无进展生存期和总生存期方面,两组间无显著差异。我们的数据表明,在接受 CAR T 细胞治疗前存在 GI 受累的患者的结局与无 GI 受累的患者相似,可以观察到持久缓解。然而,在 CAR T 细胞输注前后,有预先存在的 GI 受累的患者有因疾病进展而穿孔的风险。