Breaking down the costs for breast cancer: Insights from Sweden's National Quality Register

Abstract

Background With emerging new technologies for diagnostics and treatment for breast cancer, there is a demand for updated breast cancer costs based on current clinical practice. The objectives of the current study were to (a) estimate recent societal costs of breast cancer in Sweden and (b) provide population-based patient-level cost estimates for health economic evaluations.

Methods This prevalence-based cost-of-illness study was based on 2019 data linking multiple Swedish national registers. The analysis employed a societal perspective considering direct health care, informal care, and productivity losses. Total costs were estimated using a bottom-up micro-costing approach. Direct costs were also estimated by subgroups, including age group, molecular subtype, breast cancer stage, and disease state defined by metastatic stage.

Findings 82,960 breast cancer patients diagnosed since 2008 were alive by the end of 2019. The annual societal cost of breast cancer in Sweden was 526 million euro, where the direct health care, informal care, and productivity losses accounted for 54%, 7%, and 40%, respectively. Costs of direct health care, including inpatient/outpatient care and prescribed drugs, varied by subgroups, where younger age, higher stage, and more adverse subtypes were associated with higher costs per patient-year. Patients with a diagnosis of de novo metastatic cancer incurred the highest cost per patient-year.

Interpretation Breast cancer represents a large economic burden in Sweden. The mean cost estimates per patient-year are informative to future health economic evaluations for breast cancer screening and treatment.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by the Swedish Research Council, VINNOVA, Swedish Cancer Society, and the European Union.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

For privacy protection, we undertook all analyses under the conditions of ethical approvals provided by the Swedish Ethical Review Authority (with approvals dnr 2019-02610 and dnr 2020-00886). Specifically, any analyses of potentially identifiable data were undertaken on secure network facilities with no reporting of results for individuals or small groups. For datasets with individual-level data, the datasets used an encrypted identifier and were pseudo-anonymised.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Footnotes

Funding: the Swedish Research Council, VINNOVA, Swedish Cancer Society, and the European Union.

Data Availability

All data produced in the present work are contained in the manuscript.

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