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:Combining Obinutuzumab With Radiation for Refractory DLBCL: Retrospective Safety and Efficacy Analysis.
Combining Obinutuzumab With Radiation for Refractory DLBCL: Retrospective Safety and Efficacy Analysis.
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在这个治疗难治性 DLBCL 患者的小型队列中,放疗联合奥妥珠单抗耐受性良好,未出现过度治疗相关毒性。
约 30% 的弥漫大 B 细胞淋巴瘤(DLBCL)患者在一线化疗后出现复发或治疗难治。无法接受强化化疗和干细胞移植或CAR-T(CAR-T)细胞疗法的患者,治疗选择有限。本研究调查复发 DLBCL 患者接受奥妥珠单抗联合针对所有病灶区域的减瘤放疗的安全性和疗效。方法与材料:对治疗难治性 DLBCL 患者进行回顾性分析。所有患者均接受针对全部难治病灶的外照射放疗,并同步及辅助使用奥妥珠单抗。根据《不良事件通用术语标准》5.0 版评估毒性,采用 Kaplan-Meier 分析计算无进展生存期和总生存期。
2016 至 2022 年间,7 例难治性 DLBCL 患者接受同步放疗和奥妥珠单抗治疗。未观察到 3 级或以上治疗相关毒性。7 例中有 4 例在放疗后首次影像检查时,放射治疗部位达到完全缓解。中位无进展生存期和总生存期均为 30 个月。
在这一小型难治性 DLBCL 患者队列中,放疗联合奥妥珠单抗耐受性良好,未见过度治疗相关毒性。该联合治疗使部分患者获得持久疾病控制和延长总生存期,且未需追加治疗。
Approximately 30% of patients with diffuse large B cell lymphoma (DLBCL) will develop relapsed or treatment-refractory disease after primary chemotherapy. Patients unable to undergo aggressive chemotherapy and stem cell transplant or chimeric antigen receptor T-cell (CAR T-cell) therapy have limited treatment options. Here, we investigated the safety and efficacy of combining obinutuzumab with cytoreductive radiation to all areas of disease in patients with relapsed DLBCL. METHODS AND MATERIALS: A retrospective review of patients with treatment refractory DLBCL was performed. All patients were treated with external beam radiation to all sites of refractory disease with concurrent and adjuvant obinutuzumab. Toxicities were evaluated based on Common Terminology Criteria for Adverse Events v5.0 criteria. Kaplan-Meier analysis was used to calculate progression-free survival and overall survival.
Between 2016 and 2022, 7 patients with refractory DLBCL were treated with concurrent radiation and obinutuzumab. No grade 3 or greater treatment-related toxicity was observed. Four of the 7 patients had a complete response at the radiated site on first postradiation imaging. The median progression-free survival and overall survival were 30 months.
In this small cohort of treatment-refractory patients with DLBCL, the combination of radiation and obinutuzumab was well tolerated without excessive treatment-related toxicity. The combination resulted in durable disease control with a prolonged overall survival without additional treatment in a subset of patients.
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