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Outcomes following relapse post allo-HCT in patients with Ph+ ALL

By Ella Dixon

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Aug 16, 2024

Learning objective: After reading this article, learners will be able to cite a new clinical development in ALL



A retrospective analysis of outcomes following relapse after allogeneic hematopoietic cell transplantation (allo-HCT) in patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) was reported in the American Journal of Hematology. The analysis included adult patients with ALL (N = 290) who received their first allo-HCT and subsequently relapsed between 2006 and 2023 at City of Hope Hospital, Duarte, US. Morphologic relapse was defined as ≥5% bone marrow (BM) blasts, extramedullary/lymph node disease (LND), or central nervous system (CNS) involvement. Measurable residual disease (MRD) relapse was defined as ≥0.01% blasts by flow cytometry or BCR::ABL1 transcripts by PCR.


Key learnings

The retrospective analysis showed that 2-year progression-free survival (PFS) and overall survival (OS) were:

  • 24.9% and 43%, respectively, in patients with systemic relapse (BM and/or isolated LND)
  • 40.0% and 70.0%, respectively, in patients with isolated CNS relapse
  • 68.4% and 83.6%, respectively, in patients with MRD-only relapse

The use of novel immunotherapies improved PFS for systemic relapses, although there was no significant difference in OS.

Ponatinib was effective against resistant ABL kinase domain mutations, but no superiority was noted over older-generation tyrosine kinase inhibitors (TKIs) when used as the first TKI post-HCT relapse. 

High relapse and treatment-related mortality were observed with second allo-HCT and donor lymphocyte infusions.

Understanding the type of relapse (morphologic vs MRD), regular monitoring for MRD, and timely intervention with potent TKIs or immunotherapies is crucial for improving post-HCT outcomes in adult patients with Ph+ ALL.

References

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