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In the Spotlight

Understanding FLT3 Inhibitor Resistance to Rationalize Combinatorial AML Therapies

Aditi Shastri, Jesus Gonzalez-Lugo and Amit Verma
Aditi Shastri
1Division of Hematologic Malignancies, Department of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
2Department of Developmental & Molecular Biology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
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  • For correspondence: ashastri@montefiore.org
Jesus Gonzalez-Lugo
1Division of Hematologic Malignancies, Department of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
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Amit Verma
1Division of Hematologic Malignancies, Department of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
2Department of Developmental & Molecular Biology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
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DOI: 10.1158/2643-3230.BCD-20-0210
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Abstract

Summary: Patients treated with Fms-like tyrosine kinase 3 (FLT3) inhibitor–based acute myeloid leukemia therapies nearly always develop resistance. In this issue, Alotaibi and colleagues describe the patterns of mutations that emerge upon relapse after FLT3 inhibitor therapy after initial response, as well as in treatment-refractory disease in a single-institution study; the findings offer insights for sequential therapies targeting the dominant clone at the time of relapse.

See related article by Alotaibi et al. (5).

Footnotes

  • Blood Cancer Discov 2021;2:1–3

  • ©2020 American Association for Cancer Research.
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This OnlineFirst version was published on December 16, 2020
doi: 10.1158/2643-3230.BCD-20-0210

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Understanding FLT3 Inhibitor Resistance to Rationalize Combinatorial AML Therapies
Aditi Shastri, Jesus Gonzalez-Lugo and Amit Verma
Blood Cancer Discov December 16 2020 DOI: 10.1158/2643-3230.BCD-20-0210

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Understanding FLT3 Inhibitor Resistance to Rationalize Combinatorial AML Therapies
Aditi Shastri, Jesus Gonzalez-Lugo and Amit Verma
Blood Cancer Discov December 16 2020 DOI: 10.1158/2643-3230.BCD-20-0210
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Blood Cancer Discovery
eISSN: 2643-3249
ISSN: 2643-3230

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