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:Favorable response of a patient with primary B/myeloid mixed phenotype acute Leukemia to CD19-CAR-T: Case report and literature review.
Favorable response of a patient with primary B/myeloid mixed phenotype acute Leukemia to CD19-CAR-T: Case report and literature review.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
依据:混合表型急性白血病(MPAL)是一种罕见且异质性较高的白血病,预后不良。目前对其最佳治疗策略尚无共识,管理存在不确定性。对于表达靶抗原的难治性MPAL患者,供者来源CAR-T(CAR-T)细胞疗法是一种潜在治疗选择。 患者情况:我们近期报告了一名61岁女性MPAL患者,并阐述了其诊断和治疗过程。 诊断:依据2016年世界卫生组织分类标准确诊MPAL。 干预措施:患者先后接受3种不同的急性淋巴细胞白血病(ALL)方案及1种急性髓系白血病(AML)方案,均未达到缓解。随后接受人源CD19靶向CAR-T 细胞治疗。 结局:患者CAR-T 治疗后成功达到完全缓解。遗憾的是,CAR-T 输注8个月后患者复发,疾病呈CD19阴性,最终死亡。 经验:该病例强调人源CD19 CAR-T 细胞疗法治疗难治性MPAL的潜在疗效和安全性。尽管该患者结局不幸,病例仍提示CAR-T 可能是对其他疗法无应答的MPAL患者的一种有希望治疗选择。仍需进一步研究以确定管理这一棘手疾病的最有效策略。
RATIONALE: Mixed phenotype acute leukemia (MPAL) is a rare and heterogeneous type of leukemia known for its poor prognosis. The optimal treatment strategy for this condition currently lacks consensus, leaving uncertainty in its management. Nonetheless, a potential therapeutic option for patients with refractory MPAL who express target antigens is donor-derived chimeric antigen receptor T (CAR-T) cell therapy. PATIENT CONCERNS: We recently reported a 61-year-old woman with MPAL and elucidated its diagnosis and treatment. DIAGNOSIS: The diagnosis of MPAL was established based on the classification of World Health Organization in 2016.
INTERVENTIONS: Despite undergoing 3 different acute lymphoblastic leukemia (ALL) regimens and 1 acute myelogenous leukemia (AML) regimen, the patient did not achieve remission. Subsequently, the patient received human CD19-targeted CAR-T cell therapy. OUTCOMES: The patient achieved a successful and complete remission after CAR-T cell therapy.
Tragically, 8 months after CAR-T infusion, the patient experienced a relapse characterized by CD19-negative disease and ultimately passed away. LESSONS: This case underscores the potential efficacy and safety of human-derived CD19 CAR-T cell therapy in treating refractory MPAL. While this particular patient outcome was unfortunate, it suggests that CAR-T cell therapy may still hold promise as a viable treatment option for MPAL patients unresponsive to other therapies.
Further research in this field is warranted to determine the most effective treatment strategies for managing this challenging disease.
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