Discontinuation of imatinib in patients with oligometastatic gastrointestinal stromal tumour who are in complete radiological remission: a prospective multicentre phase II study

Authors

  • Ivar Hompland Department of Oncology, Oslo University Hospital, Oslo, Norway
  • KJetil Boye Department of Oncology, Oslo University Hospital, Oslo, Norway
  • Anne Marit Wiedswang Department of Radiology, Oslo University Hospital, Oslo, Norway
  • Andri Papakonstantinou Department of Breast Cancer, Endocrine Tumors and Sarcoma, Karolinska University Hospital, Stockholm, Sweden; Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden
  • Bård Røsok Department of Hepato-Pancreatic-Biliary Surgery, Oslo University Hospital, Oslo, Norway
  • Heikki Joensuu Comprehensive Cancer Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland
  • Øyvind Bruland Department of Oncology, Oslo University Hospital, Oslo, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway

DOI:

https://doi.org/10.2340/1651-226X.2024.39851

Keywords:

Gastrointestinal stromal tumour, GIST, imatinib, Oligometastatic disease, Survival, Quality of Life

Abstract

Introduction: Metastatic gastrointestinal stromal tumour (GIST) is considered incurable, and life-long treatment with tyrosine kinase inhibitors is recommended. We investigated whether selected patients with metastatic GIST may remain in durable remission despite imatinib discontinuation.

Patients: In this 1-group, prospective, multicentre phase II trial selected patients with oligometastatic (≤3 metastases) GIST discontinued imatinib treatment. Eligible patients had been treated with imatinib >5 years without progression and had no radiologically detectable metastases after metastasectomy, radiofrequency ablation (RFA) or complete response to imatinib. The primary endpoint was progression-free survival (PFS) 3-years after stopping imatinib. Overall survival (OS) and quality of life (QoL) were secondary endpoints.

Results: The trial closed prematurely due to slow accrual. Between January 5, 2017, and June 5, 2019, 13 patients were enrolled, of whom 12 discontinued imatinib. The median follow-up time was 55 months (range, 36 to 69) after study entry. Five (42%) of the 12 eligible patients remained progression free, and seven (58%) progressed with a median time to progression 10 months. Median PFS was 23 months and the estimated 3-year PFS 41%. Six of the seven patients who progressed restarted imatinib, and all six responded. Three-year OS was 100%, and all patients were alive at the time of the study analysis. QoL measured 5 and 11 months after discontinuation of imatinib demonstrated improvement compared to the baseline.

Interpretation: A substantial proportion of selected patients with oligometastatic GIST treated with imatinib and metastasis surgery/RFA may remain disease-free for ≥3 years with improved QoL after stopping of imatinib.

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Published

2024-05-07

How to Cite

Hompland, I., Boye, K., Wiedswang, A. M. ., Papakonstantinou, A. ., Røsok, B. ., Joensuu, H. ., & Bruland, Øyvind. (2024). Discontinuation of imatinib in patients with oligometastatic gastrointestinal stromal tumour who are in complete radiological remission: a prospective multicentre phase II study. Acta Oncologica, 63(1), 288–293. https://doi.org/10.2340/1651-226X.2024.39851