Advancements in Therapy for Acute Lymphoblastic Leukemia: Blinatumomab

نویسندگان

  • Lindsay Hladnik,1
  • Kristan Augustin,2
  • Sean DeFrates,3
چکیده

© 2016 Harborside Press® Acute lymphoblastic leukemia (ALL) is a rare form of leukemia, with an estimated 6,250 new cases diagnosed in the United States in 2015 and approximately 1,450 deaths (American Cancer Society, 2015). With current available induction therapies, complete remission (CR) rates in adults are approximately 75% to 90% (Faderl et al., 2010; Bassan & Hoelzer, 2011). After induction therapy, patients with ALL may then receive intensification, consolidation, and maintenance courses of chemotherapy or allogeneic hematopoietic stem cell transplant (HSCT). Although CR is obtained in the majority of patients with ALL, maintaining a durable CR is challenging despite the numerous phases of therapy. Standard chemotherapy regimens have resulted in an average cure rate of only 35% (Bassan & Hoelzer, 2011). There are limited treatment options for patients with relapsed or refractory Philadelphia chromosome– negative (Ph–) ALL. Options may include enrollment into clinical trials or singleor multiagent chemotherapy regimens. Historically, these patients have had very poor outcomes, with reported CR rates of approximately 20% to 30% and a median overall survival (OS) of 3 to 6 months (National Comprehensive Cancer Network [NCCN], 2014; Topp et al., 2015). Given the poor outcomes seen with chemotherapy regimens in this setting, novel agents, such as blinatumomab (Blincyto), with alternative mechanisms of action are needed.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016