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B 细胞急性淋巴细胞白血病中的新型单克隆抗体和酪氨酸激酶抑制剂。

New monoclonal antibodies and tyrosine kinase inhibitors in B-cell acute lymphoblastic leukemia.

机构信息

Hematology Unit and Romagna Transplant Network, "Santa Maria delle Croci" Hospital, Ravenna, Italy -

Hematology Unit and Romagna Transplant Network, "Santa Maria delle Croci" Hospital, Ravenna, Italy.

出版信息

Minerva Med. 2020 Oct;111(5):478-490. doi: 10.23736/S0026-4806.20.07031-7. Epub 2020 Sep 21.

Abstract

Patients with acute lymphoblastic leukemia (ALL) are characterized by an unfavorable outcome in the majority of adult cases. Several clinical trials have confirmed the usefulness of a pediatric-type therapy applied to adult patients. Adults present with higher risk features at diagnosis that predispose them to chemotherapy resistance and disease relapse after an initial achievement of complete remission. The recent introduction of novel immune-targeted therapies, including monoclonal antibodies (MoAbs) targeting B cell-associated antigens such as CD19 (blinatumumab) and CD22 (inotuzumab), tyrosine kinase inhibitors targeting BCR-ABL1 tyrosine kinase, bispecific antibodies and chimeric antigen receptor T- cell therapy (CAR-T), circumvent B-ALL cell chemo-refractoriness through novel mechanisms of action, potentially eradicating minimal residual disease (MRD) and enabling more patients to receive allogeneic hematopoietic stem cell transplantation and to achieve a better clinical outcome.

摘要

急性淋巴细胞白血病(ALL)患者在大多数成人病例中预后不良。多项临床试验证实了将儿科治疗方案应用于成年患者的有效性。成人在诊断时具有更高的风险特征,这使他们更容易对化疗产生耐药性,并在初始完全缓解后疾病复发。最近引入了新型免疫靶向治疗方法,包括针对 B 细胞相关抗原(如 CD19 [blinatumumab]和 CD22 [inotuzumab])的单克隆抗体(MoAbs)、针对 BCR-ABL1 酪氨酸激酶的酪氨酸激酶抑制剂、双特异性抗体和嵌合抗原受体 T 细胞疗法(CAR-T),通过新型作用机制规避 B-ALL 细胞的化疗耐药性,有可能根除微小残留病(MRD),使更多患者能够接受同种异体造血干细胞移植,并获得更好的临床结局。

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