Journal
CURRENT ONCOLOGY REPORTS
Volume 23, Issue 8, Pages -Publisher
SPRINGER
DOI: 10.1007/s11912-021-01086-y
Keywords
Philadelphia chromosome; ALL; Tyrosine kinase inhibitor; Stem cell transplant; Minimal residual disease
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Over the past two decades, tyrosine kinase inhibitors (TKIs) have significantly improved the outcome of patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL). The development of more potent TKIs and novel therapeutic options has changed the role of allogeneic hematopoietic stem cell transplant (alloHSCT) and intensive chemotherapy in the treatment of Ph+ ALL. An individualized, targeted approach to therapy, including monitoring of measurable residual disease (MRD), is becoming increasingly important in the management of Ph+ ALL.
Purpose of Review Over the past two decades, tyrosine kinase inhibitors (TKIs) have changed the management of patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL), and this has led to significant improvement in their outcome. In this review, we will provide an overview of the current understanding of treatment of Ph+ ALL focusing on TKIs, alloHSCT, and novel therapies. Recent findings The advent of more potent TKIs and the novel therapeutic options including blinatumomab, inotuzumab ozogamicin, and CD19 CAR-T therapy has changed the role of allogeneic hematopoietic stem cell transplant (alloHSCT) and intensive chemotherapy. To avoid toxicity from the historical treatment strategies, a more individualized, targeted approach to therapy including detection and monitoring of measurable residual disease (MRD) has become of interest. The treatment of patients with Ph+ ALL has been rapidly evolving with a more individualized, targeted treatment and use of TKIs and novel therapy.
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