How much is life worth: cetuximab, non-small cell lung cancer, and the $440 billion question
Open accessAbstract
The spiraling cost of cancer care, in particular the cost of cancer therapeutics that achieve only marginal benefits, is under increasing scrutiny. Although health-care professionals avoid putting a value on a life, our limited resources require that society address what counts as a benefit, the extent to which cost should factor in deliberations, and who should be involved in these decisions. Professional societies, such as the American Society of Clinical Oncology, government agencies, including the Food and Drug Administration, and insurance companies should be involved. However, no segment of society is better qualified to address these issues than the oncology community. Oncologists must offer clear guidance for the conduct of research, interpretation of results, and prescription of chemotherapies. We review recent drug approvals and clinical trials and comment on their relevance to the issue of the spiraling cost of oncology therapeutics. We suggest some standards that would serve as a starting point for addressing these issues.
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If treatment costs rise by 2% per year, US cancer treatment and care costs could reach US$173 billion, a 39% increase.
“If treatment costs rise by 2% a year, the overall cost of treatment and care – in the US alone – could reach US$173 billion, a 39% increase.”
US cancer treatment and care costs were projected to rise by 23% between 2010 and 2020, from US$128 billion to US$158 billion, based only on demographic change and with fixed incidence, survival and treatment costs.
“The costs of cancer treatment and care in the US alone were projected to rise by 23% between 2010 and 2020, from US$128 to US$158 billion, solely on the basis of demographic change, and with fixed incidence rates, survival probabilities and treatment costs.101”
Overestimating or overstating benefits from new interventions can cause harm, including confounding public policy, undermining research credibility, harming patients, and fueling inappropriate hype.
“Overestimating or overstating the benefits from new intervention can cause harm: it confounds public policy decision making [29], undermines the credibility of oncology research reporting [26,29,30], harms patients who choose to undertake treatments based on exaggerated expectations that may subject them to either risk of adverse effects, inconvenience or substantial personal costs [26,28] and, in”
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- Authors
- Fojo, T., & Grady, C.
- Affiliations
- National Institutes of Health (US)
- Venue
- JNCI Journal of the National Cancer Institute
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-06-29
- Volume
- 101
- Issue
- 15
- Pages
- 1044-1048
- ISSN
- 0027-8874 (ISSN-L)
- 1460-2105
- PMC
- PMC2724853
- OpenAlex
- W2135630936
- Cited by
- 349
- References
- 24
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 4 · 2023: 4 · 2022: 2 · 2021: 3 · 2020: 13 · 2019: 9 · 2018: 12 · 2017: 22 · 2016: 22 · 2015: 23 · 2014: 44 · 2013: 38 · 2012: 47
- FWCI
- 110.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- JNCI Journal of the National Cancer Institute (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Topics
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Economic and Financial Impacts of Cancer
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Pharmaceutical Economics and Policy
- Keywords
- cetuximab, non-small cell lung cancer, drug costs, value of life, cost-effectiveness, cancer therapeutics, drug approval, clinical trials, oncology prescribing, healthcare resource allocation
- MeSH terms
- Cetuximab, Antibodies, Monoclonal, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Carcinoma, Non-Small-Cell Lung, Cost-Benefit Analysis, Drug Industry, Humans, Lung Neoplasms, Neoplasms, Public Opinion, United States, United States Food and Drug Administration, Survival Analysis, Drug Costs, Treatment Outcome, Drug Approval, Clinical Trials, Phase III as Topic, Disease-Free Survival, Quality-Adjusted Life Years, Value of Life, Antibodies, Monoclonal, Humanized, ErbB Receptors
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