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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.
Background And Purpose:
In Norway, comprehensive molecular tumour profiling is implemented as part of the public healthcare system. A substantial number of tumours harbour potentially targetable molecular alterations. Therapy outcomes may improve if targeted treatments are matched with actionable genomic alterations. In the IMPRESS-Norway trial (NCT04817956), patients are treated with drugs outside the labelled indication based on their tumours molecular profile.
Patients And Methods:
IMPRESS-Norway is a national, prospective, non-randomised, precision cancer medicine trial, offering treatment to patients with advanced-stage disease, progressing on standard treatment. Comprehensive next-generation sequencing, TruSight Oncology 500, is used for screening. Patients with tumours harbouring molecular alterations with matched targeted therapies available in IMPRESS-Norway, are offered treatment. Currently, 24 drugs are available in the study. Primary study endpoints are percentage of patients offered treatment in the trial, and disease control rate (DCR) defined as complete or partial response or stable disease in evaluable patients at 16 weeks (W16) of treatment. Secondary endpoint presented is DCR in all treated patients.
Results:
Between April 2021 and October 2023, 1,167 patients were screened, and an actionable mutation with matching drug was identified for 358 patients. By the data cut off 186 patients have initiated treatment, 170 had a minimum follow-up time of 16 weeks, and 145 also had evaluable disease. In patients with evaluable disease, the DCR was 40% (58/145). Secondary endpoint analysis of DCR in all treated patients, showed DCR of 34% (58/170).
Interpretation:
Precision cancer medicine demonstrates encouraging clinical effect in a subset of patients included in the IMPRESS-Norway trial.
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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