New Insights on Management of Acute Lymphoblastic Leukemia in the Contemporary Era

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 163

Special Issue Editor


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Guest Editor
Division of Hematology-Oncology, Mayo Clinic, Jacksonville, FL, USA
Interests: acute leukemia; myeloid disorders; cellular therapy

Special Issue Information

Dear Colleagues,

Acute lymphoblastic leukemia (ALL) is commonly seen in children and tends to have an excellent outcome. In adults, it is more challenging to treat due to inherent resistance to conventional cytotoxic therapies and frequent relapses and suboptimal tolerance to intensive chemotherapy especially in elderly with high morbidity and mortality. Over the last decade, we have seen improvement in the outcomes of adult with ALL by incorporating newer antibody constructs, including antibody–drug conjugates, bispecific antibodies, and chimeric antigen receptor T-cell (CAR T-cell) therapies. We have seen significant improvements in the outcome of Philadelphia chromosome positive (Ph+) B-cell ALL with the incorporation of potent BCR-ABL1 tyrosine kinase inhibitor (TKI) combinations, and now, patients are able to achieve better and more durable responses with an improvement in long-term outcome. We have also seen advancement in our ability to assess response to therapy with the use of extremely sensitive measurable residual disease assays including clonoSEQ and next-generation sequencing (NGS), which have helped in our treatment approach. While the outcome of patients with B-cell ALL has improved, we continue to face challenges in managing T-cell ALL especially the one associated with relapsed disease. In this issue, we will highlight the current status of ALL management by focusing on challenges and opportunities.

Dr. Talha Badar
Guest Editor

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Keywords

  • B-cell ALL
  • T-cell ALL
  • MRD in ALL
  • Ph+ve ALL
  • CAR T-cells
  • NGS-MRD
  • menin inhibitors
  • blinatumomab
  • inotuzumab
  • ponatinib
  • BCR-ABL1
  • TKI

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