IMPRESS-Norway: improving public cancer care by implementing precision medicine in Norway; inclusion rates and

Katarina Puco1, Gro Live Fagereng1, Sigmund Brabrand2

  • 1Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

Abstract

Insights

Precision cancer medicine in Norway shows promise, matching targeted therapies to tumor molecular profiles. The IMPRESS-Norway trial found a 40% disease control rate in evaluable patients, indicating improved outcomes for some with advanced cancer.

Area of Science:

  • Oncology
  • Genomics
  • Precision Medicine

Background:

  • Norway integrates comprehensive molecular tumor profiling into its public healthcare system.
  • A significant number of tumors exhibit potentially targetable molecular alterations.
  • Matching targeted treatments to genomic alterations can improve therapy outcomes.

Purpose of the Study:

  • To evaluate the effectiveness of precision cancer medicine in Norway through the IMPRESS-Norway trial.
  • To assess the disease control rate (DCR) in patients with advanced cancer treated with targeted therapies based on molecular profiling.

Main Methods:

  • The IMPRESS-Norway trial is a prospective, non-randomized study for advanced-stage cancer patients progressing on standard treatment.
  • Comprehensive next-generation sequencing (TruSight Oncology 500) is used for molecular profiling.
  • Patients receive targeted therapies matched to their tumor's molecular alterations, with 24 drugs currently available.

Main Results:

  • Between April 2021 and October 2023, 1,167 patients were screened, identifying actionable mutations for 358.
  • 186 patients initiated treatment, with 170 having at least 16 weeks of follow-up.
  • The disease control rate (DCR) was 40% (58/145) in evaluable patients and 34% (58/170) in all treated patients.

Conclusions:

  • Precision cancer medicine, guided by molecular tumor profiling, shows encouraging clinical effects in a subset of patients.
  • The IMPRESS-Norway trial demonstrates the feasibility and potential benefit of matching targeted therapies to genomic alterations within a public healthcare system.

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