肿瘤细胞治疗研究
英文原题:Case report: Cryoablation as a novel bridging strategy prior to CAR-T cell therapy for B cell malignancies with bulky disease.
Case report: Cryoablation as a novel bridging strategy prior to CAR-T cell therapy for B cell malignancies with bulky disease.
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嵌合抗原受体(CAR)T细胞疗法已成为治疗复发/难治性(R/R)血液系统恶性肿瘤的强效免疫疗法,尤其用于R/R B细胞急性淋巴细胞白血病(B-ALL)、非霍奇金淋巴瘤(NHL)和多发性骨髓瘤(MM)。在CAR-T 细胞制备期间,为防止疾病进展并降低肿瘤负荷,输注前桥接治疗至关重要。目前已证明靶向治疗、放疗和自体干细胞移植(ASCT)可作为有效桥接策略。但冷冻消融能否作为新型桥接策略尚不明确。本文报告2例大肿块R/R B细胞恶性肿瘤患者,成功接受冷冻消融联合CAR-T 细胞治疗。患者1为65岁女性,确诊伴髓外病变(EMD)的R/R MM,并入组抗BCMA CAR-T 细胞临床试验。患者2为70岁男性,右大腿前方出现皮下肿块,一年前确诊原发性皮肤弥漫大B细胞淋巴瘤腿型(PCLBCL-LT);患者对多线化疗及放疗均失败,因此申请接受抗CD19 CAR-T 细胞治疗。两名患者均在CAR-T 细胞制备期间出现局部进展。为快速控制局部肿瘤并降低肿瘤负荷,两人均接受冷冻消融桥接治疗。患者1在CAR-T 细胞输注后1个月达到非常好的部分缓解(VGPR);患者2在输注后1个月达到部分缓解(PR)。
此外,不良反应均可耐受和管理。本研究首次证明冷冻消融联合CAR-T 细胞治疗具有良好安全性和疗效,也提示冷冻消融可作为控制B细胞恶性肿瘤局部病灶的新治疗策略。
Chimeric antigen receptor (CAR) T-cell therapy has emerged as a powerful immunotherapy in relapsed/refractory (R/R) hematological malignancies, especially in R/R B-cell acute lymphocytic leukemia (B-ALL), non-Hodgkin lymphoma (NHL), and multiple myeloma (MM).
To prevent disease progression and reduce tumor burden during CAR-T cell manufacturing, bridging therapies prior to CAR-T cell infusion are crucial. At present, it has been demonstrated that targeted therapy, radiotherapy and autologous stem cell transplantation (ASCT) could serve as effective bridging strategies.
However, whether cryoablation could serve as a novel bridging strategy is unknown. In this paper, we report 2 cases of R/R B cell malignancies with bulky disease that were successfully treated with a combination of cryoablation and CAR-T cell therapy. Patient 1 was a 65-year-old female who was diagnosed with R/R MM with extramedullary disease (EMD).
She was enrolled in the anti-BCMA CAR-T cell clinical trial. Patient 2 was a 70-year-old man who presented with a subcutaneous mass in the right anterior thigh and was diagnosed with primary cutaneous diffuse large B cell lymphoma, leg type (PCLBCL-LT) 1 year ago. He failed multiline chemotherapies as well as radiotherapy.
Thus, he requested anti-CD19 CAR-T cell therapy. Unfortunately, they all experienced local progression during CAR-T cell manufacturing. To rapidly achieve local tumor control and reduce tumor burden, they both received cryoablation as a bridging therapy. Patient 1 achieved a very good partial response (VGPR) 1 month after CAR-T cell infusion, and patient 2 achieved a partial response (PR) 1 month after CAR-T cell infusion.
In addition, adverse effects were tolerable and manageable.
Our study demonstrated the favorable safety and efficacy of combination therapy with cryoablation and CAR-T cell therapy for the first time, and it also indicates that cryoablation could serve as a novel therapeutic strategy for local tumor control in B cell malignancies.
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