不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Hematopoietic recovery and immune reconstitution after axicabtagene ciloleucel in patients with large B-cell lymphoma.
Hematopoietic recovery and immune reconstitution after axicabtagene ciloleucel in patients with large B-cell lymphoma.
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靶向 CD19 的嵌合抗原受体(CAR)T 细胞治疗可能伴随长期不良影响,如血细胞减少和免疫缺陷。为描述这些迟发事件,我们分析了本院两项临床试验 ZUMA-1(NCT02348216)和 ZUMA-9(NCT03153462)中接受 axicabtagene ciloleucel 治疗的 31 例复发/难治性大 B 细胞淋巴瘤患者。连续监测全血细胞计数、淋巴细胞亚群和免疫球蛋白水平,直至第 24 个月或疾病进展。第 30 天,15 例(48%)出现 3–4 级血细胞减少,包括贫血 5 例(16%)、中性粒细胞减少 9 例(29%)和血小板减少 13 例(42%)。
第 30 天的血细胞减少与之后诊断骨髓增生异常综合征无显著相关。在持续缓解患者中,2 年时 9 例中有 1 例(11%)出现 3–4 级血细胞减少。外周 CD8⁺ T 细胞较早恢复,而 CD4⁺ T 细胞恢复延迟:1 年时 9 例中有 3 例(33%)、2 年时 7 例中有 2 例(29%)计数低于 200/mL。2 年时 9 例中有 5 例(56%)免疫球蛋白 G 水平恢复正常。13 例(42%)发生 3–4 级感染并发症,包括带状疱疹和耶氏肺孢子菌肺炎。这些结果提示,应对患者进行长期监测并预防机会性感染,以提高 axicabtagene ciloleucel 治疗的长期安全性。
Chimeric antigen receptor (CAR) T-cell therapy targeting CD19 may be associated with long-term adverse effects such as cytopenia and immune deficiency. In order to characterize these late events, we analyzed 31 patients with relapsed or refractory large B-cell lymphoma treated with axicabtagene ciloleucel at our institution on two clinical trials, ZUMA-1 (clinicaltrials gov. Identifier: NCT02348216) and ZUMA-9 (clinicaltrials gov. Identifier: NCT03153462). Complete blood counts, lymphocyte subsets, and immunoglobulin levels were measured serially until month 24 or progression. Fifteen (48%) patients had grade 3-4 cytopenia, including anemia (five, 16%), neutropenia (nine, 29%), or thrombocytopenia (13, 42%) at day 30.
Cytopenia at day 30 was not significantly associated with later diagnosis of myelodysplasia. Among patients with ongoing remission, grade 3-4 cytopenia was observed in one of nine (11%) at 2 years. While peripheral CD8+ T cells recovered early, CD4+ T-cell recovery was delayed with a count of <200/mL in three of nine (33%) patients at 1 year and two of seven (29%) at 2 years.
Immunoglobulin G levels normalized in five of nine (56%) patients at 2 years. Thirteen (42%) patients developed grade 3-4 infectious complications, including herpes zoster and Pneumocystis jiroveci pneumonia. These results suggest the need for prolonged monitoring and prophylaxis against opportunistic infections in these patients, to improve the longterm safety of axicabtagene ciloleucel therapy.
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