CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Late hematologic toxicity after CAR T-cell therapy in large B-cell lymphoma: incidence, risk factors, and clinical impact.
Late hematologic toxicity after CAR T-cell therapy in large B-cell lymphoma: incidence, risk factors, and clinical impact.
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晚期免疫效应细胞相关血液毒性(ICAHT)是 CAR-T 治疗后公认的并发症,但其发生率和临床后果仍不明确。我们评估了 290 例接受 CAR-T 治疗的大 B 细胞淋巴瘤患者的早期和晚期血液毒性。早期 ICAHT(输注后 30 天)发生于 78% 的患者(1 级:22%,2 级:26%,3 级:22%,4 级:8.1%)。至第 100 天时,晚期 ICAHT(输注后 > 30 天)的累积发生率分别为:任何级别 45%(95% CI 39-51),2 级 40%(95% CI 34-46),3 级 22%(95% CI 17-27),4 级 7.2%(95% CI 4.4-11)。
第 100 天时晚期中重度血小板减少症(< 50 10 3 / L)和贫血(< 8 g/dL)的累积发生率分别为 20%(95% CI 15-25)和 14%(95% CI 10-19)。早期重度 ICAHT(3 级)与晚期重度 ICAHT(p < 0.001)、晚期重度血小板减少症(p < 0.001)和晚期中重度贫血(p = 0.037)独立相关。晚期重度 ICAHT 与晚期感染风险增加相关(HR 2.85 [95% CI 1.18-6.88],p = 0.032)。这些发现突出表明,晚期血液学毒性是 CAR-T 治疗中常见且具有临床相关性的并发症。将 ICAHT 分级纳入输注后监测可能有助于制定预防策略,以减轻长期并发症。
Late Immune Effector Cell-Associated HematoToxicity (ICAHT) is a recognized complication following CAR T therapy, yet their incidence and clinical consequences remain poorly defined.
We assessed early and late hematotoxicity in 290 patients with large B-cell lymphoma receiving CAR T therapy. Early ICAHT ( 30 days post-infusion) occurred in 78% of patients (grade 1: 22%, grade 2: 26%, grade 3: 22%, grade 4: 8. 1%). Cumulative incidence of late ICAHT ( > 30 days post-infusion) by day 100 was 45% (95% CI 39-51) for any grade, 40% (95% CI 34-46) for grade 2, 22% (95% CI 17-27) for grade 3, and 7. 2% (95% CI 4. 4-11) for grade 4.
Cumulative incidences of late moderate-severe thrombocytopenia ( < 50 10 3 / L) and anemia ( < 8 g/dL) at day 100 were 20% (95% CI 15-25) and 14% (95% CI 10-19), respectively. Early severe ICAHT (grade 3) was independently associated with late severe ICAHT (p < 0. 001), late severe thrombocytopenia (p < 0. 001), and late moderate-severe anemia (p = 0. 037). Late severe ICAHT was associated with an increased hazard of late infections (HR 2. 85 [95% CI 1. 18-6. 88], p = 0. 032).
These findings highlight late hematologic toxicity as a frequent and clinically relevant complication of CAR T therapy. Incorporating ICAHT grading into post-infusion monitoring may inform preventive strategies to mitigate long-term complications.
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