医学
阿糖胞苷
奥佐美星
米多司他林
柔红霉素
髓系白血病
肿瘤科
内科学
化疗
诱导化疗
重症监护医学
干细胞
CD33
川地34
遗传学
生物
作者
Kenny Tang,Andre C. Schuh,Karen Yee
标识
DOI:10.1007/s11912-021-01108-9
摘要
With the recent approval of multiple new drugs for the treatment of acute myeloid leukemia (AML), the relevance of conventional treatment approaches, such as daunorubicin and cytarabine (“3+7”) induction chemotherapy, has been challenged. We review the AML risk stratification, the efficacy of the newly approved drugs, and the role of “3+7”. Treatment of AML is becoming more niched with specific subtypes more appropriately treated with gemtuzumab, midostaurin, and CPX-351. Although lower intensity therapies can yield high response rates, they are less efficient at preventing relapses. The only curative potential for poor-risk AML is still an allogeneic stem cell transplant. The number of AML subtypes where 3+7 alone is an appropriate therapeutic option is shrinking. However, it remains the backbone for combination therapy with newer agents in patients suitable for intensive chemotherapy.
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