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Published on: February 12, 2017
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.
Abstract:
Little is known about outcomes following interruption of targeted therapy in adult patients with histiocytic neoplasms. This is an IRB-approved study of patients with histiocytic neoplasms whose BRAF and MEK inhibitors were interrupted after achieving complete or partial response by 18-fluorodeoxyglucose positron emission tomography (FDG-PET). 17/22 (77%) of patients experienced disease relapse following treatment interruption. Achieving a complete response prior to interruption, having a mutation other than BRAFV600E, and receiving MEK inhibition only were each associated with a statistically significant improvement in relapse-free survival. Relapse is common following treatment interruption however some patients may be suitable for limited-duration treatment.
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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