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:BRIDGE-2M: Optimizing Bridging Therapy Prior to CAR-T Therapy in Multiple Myeloma: A Modified Double-Blind Delphi Panel of US Physicians.
BRIDGE-2M: Optimizing Bridging Therapy Prior to CAR-T Therapy in Multiple Myeloma: A Modified Double-Blind Delphi Panel of US Physicians.
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本研究综合专家医师观点,构建了一套基于共识的框架以优化 BT 选择,将五项关键患者特征与临床目标相关联,其目标不仅限于疾病稳定,还扩展至提升 CAR-T 疗效与安全性。本文提供图文摘要,见 10.6084/m9.figshare.33016328。
我们旨在就复发/难治性多发性骨髓瘤(RRMM)患者接受CAR-T 细胞治疗时的最佳桥接治疗(BT)选择达成共识。
我们在美国从事RRMM治疗的血液肿瘤科/血液科医生中开展了一项双盲、三轮改良Delphi专家小组研究,这些医生均使用CAR-T 疗法。
专家组成员(N = 15;所有人在过去一年内管理 60-100 例 RRMM 患者;> 5 年执业经验:86.7%)就影响 BT 选择的关键属性达成共识(疾病负荷、侵袭性疾病、体能状态、合并症、治疗线数、年龄、衰弱)。特定的患者属性与临床目标相关联(65 岁或衰弱:疾病稳定 [71% 共识];体能状态差:终末器官功能保护;合并症:功能保留;高疾病负荷:预防临床衰退;侵袭性疾病:细胞减灭 [均 100% 共识])。BT 的目标是降低疾病负荷并促进 CAR-T 疗效和安全性(100% 共识)。虽然 talquetamab 在后线中作为桥接治疗更受青睐(66.7%),但若获批,73.3% 会考虑更早线使用。
We conducted a double-blind, three-round modified Delphi panel among U.S.-based hematologist-oncologists/hematologists using CAR-T therapy for RRMM.
Panelists (N = 15; all managing -60-100 patients with RRMM within the past year; > 5 years of practice: 86.7%) reached consensus on key attributes influencing BT selection (disease burden, aggressive disease, performance status, comorbidities, line of therapy, age, frailty). Unique patient attributes were linked to clinical objectives ( 65 years or frailty: disease stabilization [71% consensus]; poor performance status: end-organ function preservation; comorbidities: functional preservation; high disease burden: preventing clinical decline; aggressive disease: cytoreduction [all 100% consensus]). Goals of BT were to decrease disease burden and promote CAR-T efficacy and safety (100% consensus). While talquetamab was preferred for bridging in later lines (66.7%), 73.3% would consider earlier-line use if approved.
This study synthesized expert physician perspectives to develop a consensus-based framework to optimize BT selection, linking five key patient attributes to clinical objectives, with goals extending beyond disease stabilization to enhancing CAR-T efficacy and safety. Graphical abstract available for this article 10.6084/m9.figshare.33016328.
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