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:On Route to Chimeric Antigen Receptor T-cell (CAR T) Therapy, Less Is More: Adaptive Bridging Radiotherapy in Large B-cell Lymphoma.
On Route to Chimeric Antigen Receptor T-cell (CAR T) Therapy, Less Is More: Adaptive Bridging Radiotherapy in Large B-cell Lymphoma.
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CD19靶向嵌合抗原受体(CAR)T细胞疗法显著推进了复发/难治性大B细胞淋巴瘤(LBCL)的治疗。在关键的4至6周等待期,直至CAR-T 细胞制备完成,放射治疗(RT)可用于控制疾病。
我们报告一例64岁女性患者,患有复发/难治性弥漫大B细胞淋巴瘤(DLBCL),在接受CAR-T 细胞治疗前,作为桥接策略,对双侧肾上腺肿块接受了适应性放疗,并纳入了一项适应性放疗临床试验。计划采用基于CT的在线适应性放疗(Varian Ethos配合HyperSight成像,Varian Medical Systems,Palo Alto,CA),每周一次,最多五次分割(每次5 Gy)。患者症状迅速缓解,且无放疗相关毒性。由于锥形束CT(CBCT)显示肿瘤显著缩小,患者仅接受了计划中一半的放疗次数(四次中的两次)。
因此,患者接受的总剂量(10 Gy)低于标准放疗可能给予的剂量。放疗后PET/CT显示疾病显著消退,符合部分缓解,随后进行CAR-T 细胞输注。本病例展示了适应性放疗作为CAR-T 细胞治疗前桥接疗法的成功应用,我们期待该适应性放疗试验的结果将指导未来在复发/难治性B细胞淋巴瘤中适应性放疗的应用。
CD19-targeted chimeric antigen receptor (CAR) T-cell therapy has appreciably advanced treatment for relapsed or refractory large B-cell lymphoma (LBCL). During the critical interim of four to six weeks, until CAR T-cells are ready, radiation therapy (RT) can be used to control the disease.
We present the case of a 64-year-old female with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) who received adaptive RT for bilateral adrenal masses as a bridging strategy before undergoing CAR T-cell therapy and enrolled in an adaptive RT clinical trial. A plan was developed to deliver up to five once-weekly fractions (5 Gy per fraction) of CT-based online adaptive RT (Varian Ethos with HyperSight imaging, Varian Medical Systems, Palo Alto, CA). The patient experienced rapid symptomatic relief, with no RT-related toxicities.
The patient received RT at only half of the sessions (two out of four sessions) due to excellent tumor shrinkage on cone-beam CT (CBCT). As such, the patient was treated at a lower total dose (10 Gy) than she otherwise would have received with standard RT.
Post-RT PET/CT showed significant disease regression, compatible with partial response, prior to CAR T-cell infusion. This case shows the successful application of adaptive RT as bridging therapy prior to CAR T-cell therapy, and we expect the results of this adaptive RT trial to guide the future of adaptive RT in relapsed/refractory B-cell lymphomas.
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