检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘文慧 吴涛 张曦 LIU Wenhui;WU Tao;ZHANG Xi(Department of Hematology,the 940th Hospital of Joint Logistics Support Force of Chinese People’s Liberation Army,Lan-zhou 730050,China;Department of Hematology,Second Affiliated Hospital of Army Medical University of Chinese People’sLiberation Army,Chongqing 400037)
机构地区:[1]中国人民解放军联勤保障部队第九四〇医院血液科,甘肃兰州730050 [2]中国人民解放军陆军军医大学第二附属医院血液科,重庆400037
出 处:《内科理论与实践》2024年第3期201-206,共6页Journal of Internal Medicine Concepts & Practice
基 金:甘肃省科技计划(创新基地和人才计划)项目(21JR7RA015);甘肃省科技计划项目(22YF7FA106);联勤保障部队第九四〇医院科研项目(2021yxky078)。
摘 要:急性淋巴细胞白血病(acute lymphoblastic leukemia,ALL)是以原始幼稚淋巴细胞异常增殖并抑制正常造血的血液系统恶性肿瘤,起源于B系或T系淋巴祖细胞,占成人急性白血病的20%~30%。虽然初诊成人ALL患者在多药联合化疗后完全缓解率可达80%以上,但仍有大部分患者最终出现复发、难治,5年长期生存率仅20%~40%,其临床特点及预后差异较大。近年来,随着靶向药物、免疫治疗、嵌合抗原受体(chimeric antigen receptor,CAR)-T细胞疗法等问世,极大地改善了成人ALL患者的临床结局。本文详细综述目前成人ALL新型治疗药物的进展。Acute lymphoblastic leukemia(ALL)is a hematological malignancy with abnormal proliferation of primitive naive lymphocytes and inhibition of normal hematopoiesis.It originates from B-lineage or T-lineage lymphoid progenitor cells,accounting for 20%-30%of adult acute leukemia.Although the complete remission rate of newly diagnosed adult ALL patients after multi-drug combination chemotherapy can reach more than 80%,most of the patients still show relapse and refractory.The 5-year long term survival rate in the patients is only 20%-40%and the clinical characteristics and prognosis are quite different.In recent years,with the advent of targeted drugs,immunotherapy,and chimeric antigen receptor(CAR)-T cell therapy,the clinical outcomes of adult ALL patients have been greatly improved.This article reviews the current progress of new therapeutic drugs for adult ALL in detail.
关 键 词:急性淋巴细胞白血病 酪氨酸激酶抑制剂 兰妥莫单抗 伊组单抗奥加米星 嵌合抗原受体T细胞 Venetoclax 奈拉滨
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.220.204.192