Evidence map›Paper›PMID 39520611›Full record

ArticleApplied health economics and health policy2025

Using Genomic Heterogeneity to Inform Therapeutic Decisions for Metastatic Colorectal Cancer: An Application of the Value of Heterogeneity Framework.

Reka E Pataky, Stuart Peacock, Stirling Bryan, Mohsen Sadatsafavi, Dean A Regier

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Article in Applied health economics and health policy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Reka E PatakyCanadian Centre for Applied Research in Cancer Control, BC Cancer, Vancouver, BC, Canada. rpataky@bccrc.ca.ORCID 0000-0003-0159-582X
Stuart PeacockCanadian Centre for Applied Research in Cancer Control, BC Cancer, Vancouver, BC, Canada.ORCID 0000-0002-8243-8721
Stirling BryanCentre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.ORCID 0000-0001-7093-3058
Mohsen SadatsafaviCollaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-0419-7862
Dean A RegierCanadian Centre for Applied Research in Cancer Control, BC Cancer, Vancouver, BC, Canada.ORCID 0000-0001-8876-0511

Funding

Genome Canada G05CHS
6 · The paper itself

Abstract

BACKGROUND AND

objectiveMutations in KRAS and NRAS are predictive of poor response to cetuximab and panitumumab, two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies used in metastatic colorectal cancer (mCRC). Our objective was to explore the value of using KRAS and NRAS mutation status to inform third-line anti-EGFR therapy for mCRC using the value of heterogeneity (VOH) framework.

methodsWe used administrative data to identify mCRC patients who were potentially eligible for third-line therapy in 2006-2019 in British Columbia (BC), Canada. We compared three alternative stratification policies in place during the study period: the unstratified policy where anti-EGFR therapy was not offered (2006-2009), stratification by KRAS mutation (2009-2016), and stratification by KRAS+NRAS mutation (2016-2019). We used inverse-probability-of-treatment weighting to balance covariates across the three groups. Cost and survival time were calculated using a 3-year time horizon and adjusted for censoring, with bootstrapping to characterize uncertainty. Mean net monetary benefit (NMB) was calculated at a range of threshold values. The VOH of using KRAS and NRAS mutation status to inform treatment selection was calculated as the change in NMB with increasing stratification, under current (static VOH) or perfect (dynamic VOH) information.

resultsWe included 2664 patients in the analysis. At a willingness-to-pay of CA$100,000/ life-year gained (LYG), stratification on KRAS mutation status provided a static VOH of CA$1565 per patient; further stratification on KRAS+NRAS provided additional static VOH of CA$594. The static VOH exceeded the marginal cost of genomic testing under both policies.

conclusionsStratification of anti-EGFR therapy by KRAS and NRAS mutation status can provide additional value at a threshold of CA$100,000/LYG. There is diminishing marginal value and increasing marginal costs as the policy becomes more stratified. The VOH framework can illustrate the value of subgroup-specific decisions in a comprehensive way, to better inform targeted treatment policies.

Indexed as

Colorectal NeoplasmsGenetic HeterogeneityAgedBritish ColumbiaCetuximabClinical Decision-MakingCost-Benefit AnalysisErbB ReceptorsFemaleGTP PhosphohydrolasesHumansMaleMembrane ProteinsMiddle AgedMutationNeoplasm MetastasisCetuximabErbB ReceptorsGTP PhosphohydrolasesKRAS protein, humanMembrane ProteinsNRAS protein, humanPanitumumabProto-Oncogene Proteins p21(ras)

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.