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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antibiotic Use Before CAR-T Treatment Is Associated with Inferior Outcomes in DLBCL Lymphoma Patients.
Antibiotic Use Before CAR-T Treatment Is Associated with Inferior Outcomes in DLBCL Lymphoma Patients.
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我们回顾性分析了 140 例患者的临床数据,以评估 CAR-T 细胞疗法前感染相关抗生素治疗的影响,并将他们分为两个队列:67 例既往有抗生素暴露和 73 例无暴露。
与无暴露的患者相比,CAR-T 治疗前暴露于抗生素的患者无进展生存期显著缩短(p = 0.016),总生存期也显著缩短(p = 0.002)。多个抗生素疗程以及最后一次抗生素治疗与 CAR-T 细胞疗法之间较短的间隔与较差的结局相关。
我们的数据表明,CAR-T 细胞治疗前抗生素暴露与较差的结局相关,尽管目前尚不清楚这种效应是因果关系还是反映了患者潜在的合并症。这些发现强调需要进一步研究抗生素诱导的菌群失调对 CAR-T 细胞疗法疗效的作用。
Background/Objectives: CAR-T-cell therapy has become a key treatment for relapsed or refractory hematologic malignancies such as diffuse large B-cell lymphoma (r/r DLBCL), although patient outcomes differ considerably. The intestinal microbiome has been proposed as an important factor influencing CAR-T-cell therapy efficacy; accordingly, antibiotic exposure, which may induce dysbiosis, has been associated with inferior outcomes after CAR-T-cell therapy. Methods: We retrospectively analyzed clinical data from 140 patients to assess the impact of infection-related antibiotic therapy prior to CAR-T-cell therapy, stratifying them into two cohorts: 67 patients with previous antibiotic exposure and 73 without exposure.
Results: Patients exposed to antibiotics prior to CAR-T therapy had significantly reduced progression-free survival ( p = 0. 016) and overall survival ( p = 0. 002) compared to those without exposure. Multiple antibiotic courses and shorter intervals between the last antibiotic treatment and CAR-T-cell therapy were linked to poorer outcomes.
Conclusions: Our data suggest that pre-CAR-T-cell-therapy antibiotic exposure is associated with inferior outcomes, although it remains unclear whether this effect is causal or reflects underlying patient comorbidities.
These findings highlight the need for further studies investigating the role of antibiotic-induced dysbiosis on CAR-T-cell therapy efficacy.
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