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A personalized approach to acute myeloid leukemia therapy: current options.
Illangeswaran, Raveen Stephen Stallon; Das, Saswati; Paul, Daniel Zechariah; Mathews, Vikram; Balasubramanian, Poonkuzhali.
Afiliação
  • Illangeswaran RSS; Department of Haematology, Christian Medical College, Vellore, India.
  • Das S; Department of Haematology, Christian Medical College, Vellore, India.
  • Paul DZ; Department of Haematology, Christian Medical College, Vellore, India.
  • Mathews V; Department of Haematology, Christian Medical College, Vellore, India.
  • Balasubramanian P; Department of Haematology, Christian Medical College, Vellore, India.
Pharmgenomics Pers Med ; 12: 167-179, 2019.
Article em En | MEDLINE | ID: mdl-31447578
Therapeutic options for acute myeloid leukemia (AML) have remained unchanged for nearly the past 5 decades, with cytarabine and anthracyclines and use of hypomethylating agents for less intensive therapy. Implementation of large-scale genomic studies in the past decade has unraveled the genetic landscape and molecular etiology of AML. The approval of several novel drugs for targeted therapy, including midostaurin, enasidenib, ivosidenib, gemtuzumab-ozogamicin, and CPX351 by the US Food and Drug Administration has widened the treatment options for clinicians treating AML. This review focuses on some of these novel therapies and other promising agents under development, along with key clinical trial findings in AML.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article