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http://dx.doi.org/10.1080/10428194.2020.1768380DOI Listing

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Article Synopsis
  • * A case study details a 75-year-old Hispanic male with relapsed/refractory Philadelphia-positive B-cell ALL, who was treated with multiple TKIs and chemotherapy, culminating in a novel combination of ponatinib and asciminib before and after brexu-cel therapy.
  • * This combination of ponatinib and asciminib proved to be effective, controlling the disease for 2 months before brexu
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Article Synopsis
  • A 46-year-old man diagnosed with chronic myeloid leukemia (CML) failed initial treatments with multiple tyrosine kinase inhibitors due to a specific mutation.
  • After starting ponatinib (PON) at age 66, he achieved a complete cytogenetic response (CCyR) within three months but faced complications leading to dosage adjustments.
  • Eventually, after experiencing a deep molecular response for three years, his treatment was restarted after losing response, and he has been maintaining his response at age 77, with improvements possibly linked to hemodialysis.
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Relapsed or refractory (r/r) Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) still represent an unmet clinical need despite the new immune therapies available for these patients. We report the case of a Ph + ALL relapsed one year after allogeneic stem cell transplant. After one DLI was started CAR-T program with brexucabtageneautoleucel, using as bridging treatment ponatinib, vincristine and prednisone.

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Progress in the research and therapy of adult acute lymphoblastic leukemia (ALL) is accelerating. This analysis summarizes the data derived from the clinical trials conducted at MD Anderson between 1985 and 2022 across ALL subtypes. In Philadelphia chromosome-positive ALL, the addition of BCR::ABL1 tyrosine kinase inhibitors (TKIs) to intensive chemotherapy since 2000, improved outcomes.

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Philadelphia (Ph)-like acute lymphoblastic leukemia (ALL) constitutes a heterogeneous subset of ALL with a uniformly unfavorable prognosis. The identification of mutations amenable to treatment with tyrosine kinase-inhibitors (TKIs) represents a promising field of investigation. We report the case of a young patient affected by relapsed/refractory Ph-like ALL treated with chimeric antigen receptor T (CAR-T) cells after successful bridging with compassionate-use ponatinib and low-dose prednisone.

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