Outcomes after interruption of targeted therapy in patients with histiocytic neoplasms

Anne S Reiner1, Benjamin H Durham2,3, Mariko Yabe2

  • 1Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

PubMed

Insights

Targeted therapy interruption for histiocytic neoplasms often leads to relapse. However, achieving complete response, having non-BRAFV600E mutations, or MEK-only inhibition may improve outcomes.

Area of Science:

  • Oncology
  • Hematology
  • Pharmacology

Background:

  • Outcomes after interrupting targeted therapy for histiocytic neoplasms are poorly understood.
  • Histiocytic neoplasms are rare and require effective treatment strategies.

Purpose of the Study:

  • To investigate disease relapse and survival following interruption of BRAF and MEK inhibitors in adult patients with histiocytic neoplasms.
  • To identify factors associated with improved relapse-free survival after treatment cessation.

Main Methods:

  • Retrospective study of 22 adult patients with histiocytic neoplasms.
  • Treatment interruption occurred after achieving complete or partial response assessed by 18-fluorodeoxyglucose positron emission tomography (FDG-PET).
  • Analysis of relapse-free survival based on response, mutation status, and treatment received.

Main Results:

  • Disease relapse occurred in 17/22 (77%) of patients after treatment interruption.
  • Complete response before interruption, non-BRAFV600E mutations, and MEK inhibition alone were linked to significantly better relapse-free survival.
  • Limited-duration targeted therapy may be feasible for select patients.

Conclusions:

  • Relapse is a frequent event after discontinuing targeted therapy for histiocytic neoplasms.
  • Patient-specific factors and treatment regimens influence the likelihood of sustained remission.
  • Further research is needed to optimize treatment duration and management strategies.

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