Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 May;23(3):441-452.
doi: 10.1007/s40258-024-00926-9. Epub 2024 Nov 9.

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

Affiliations

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

Reka E Pataky et al. Appl Health Econ Health Policy. 2025 May.

Abstract

Background and objective: Mutations 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.

Methods: We 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.

Results: We 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.

Conclusions: Stratification 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.

PubMed Disclaimer

Conflict of interest statement

Declarations. Funding: REP was supported by a Canadian Institutes of Health Research Doctoral Research Award. The Canadian Network for Learning Healthcare Systems and Cost-effective ‘Omics Innovation (CLEO) is supported by Genome BC/Genome Canada [G05CHS]. The funders were not involved in the writing of the manuscript or the decision to submit it for publication. Declaration of Interests: DAR’s institution has received research funding for a project from Roche Canada and DAR has received travel funding from Illumina. REP, MS, SB and SP declare that they have no conflict of interest. Authors’ Contributions: REP and DAR conceptualized the study. REP acquired data and conducted data analysis, with review and verification by DAR. All authors contributed to review and interpretation of results. REP wrote the initial draft, and all authors conducted critical review and revision of the manuscript. Data Access: Access to data provided by the Data Stewards is subject to approval but can be requested for research projects through the Data Stewards or their designated service providers. The following data sets were used in this study: BC Cancer Registry, Population Data BC Consolidation File (Registration and Premium Billing), Hospital Separations (Discharge Abstracts Database), Medical Services Plan (MSP) Payment Information File, Vital Statistics Deaths File, and PharmaNet. You can find further information regarding these data sets by visiting the PopData project webpage at: https://my.popdata.bc.ca/project_listings/17-077/collection_approval_dates . All inferences, opinions, and conclusions drawn in this publication are those of the author(s) and do not reflect the opinions or policies of the Data Steward(s). Ethics Approval: This study was approved by the University of British Columbia-BC Cancer Research Ethics Board, certificate H15-03418. Consent to Participate: Not applicable. Consent for Publication from Patients/Participants: Not applicable. Code Availability: Code is available by request from the corresponding author.

Similar articles

Cited by

References

    1. Jonker DJ, et al. Cetuximab for the treatment of colorectal cancer. N Engl J Med. 2007;357(20):2040–8. - PubMed - DOI
    1. Sobrero AF, et al. EPIC: phase III Trial of Cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26(14):2311–9. - PubMed - DOI
    1. Van Cutsem E, et al. Open-label phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. J Clin Oncol. 2007;25(13):1658–64. - PubMed - DOI
    1. Amado RG, et al. Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26(10):1626–34. - PubMed - DOI
    1. Lien K, et al. The use of EGFR inhibitors in colorectal cancer: is it clinically efficacious and cost-effective? Expert Rev Pharmacoecon Outcomes Res. 2015;15(1):81–100. - PubMed - DOI

MeSH terms

Grants and funding

LinkOut - more resources