Comparative and Cost Effectiveness of Treatment Modalities for Hepatocellular Carcinoma in SEER-Medicare
Overview
Affiliations
Background: The incidence of hepatocellular carcinoma (HCC) is increasing in the USA and worldwide. Several treatments are available for patients diagnosed at any disease stage. It remains unclear how medical expenditures vary across patients who remain untreated or undergo different modes of therapy. We evaluate the comparative and cost effectiveness of treatment modalities for HCC from a Medicare perspective.
Methods: The Surveillance, Epidemiology, and End Results (SEER) registries and linked Medicare database with claims from Parts A/B were used to identify Medicare enrollees with initial diagnosis of HCC between 2000 and 2007 and followed through 2009. Patients were assigned to treatment modalities based on HCC staging systems: transplant, resection, liver directed, radiation, chemotherapy or no treatment. Survival benefits and cumulative Medicare expenditures were estimated in multivariate models, stratified by initial disease stage, to control for confounding. Cost-effectiveness ratios compared costs and benefits of the modalities across initial stages.
Results: Cancer stages I, II, III, IV and unstaged represented 24, 9, 14, 17 and 37 % of 11,047 patients, respectively. Fewer than 40 % received any treatment. Relative to no treatment, transplant was most effective in reducing mortality, followed by resection, liver directed, and radiation or chemotherapy. Resection tended to be most cost effective in early staged and unstaged patients; transplant was least cost effective. In stage IV patients, liver directed therapy was more cost effective than chemotherapy or radiation.
Conclusions: Survival benefit was attributable to all treatment modalities. More effective treatments incurred greater Medicare expenditures, but resection patients incurred the least expenditures per year of life gained.
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Zhao M, Guo Z, Zou Y, Li X, Yan Z, Chen M Hepatol Int. 2023; 18(1):4-31.
PMID: 37864725 DOI: 10.1007/s12072-023-10599-6.
Li B, Qiu J, Zheng Y, Shi Y, Zou R, He W Ann Surg Open. 2023; 2(2):e057.
PMID: 37636551 PMC: 10455427. DOI: 10.1097/AS9.0000000000000057.
Soheilipour M, Kazemi M, Taheri B, Adibi P, Abdollahpour I Adv Biomed Res. 2023; 12:115.
PMID: 37288022 PMC: 10241624. DOI: 10.4103/abr.abr_230_21.
Tan J, Yu Y, Lin X, He Y, Jin W, Qian H Hepatol Int. 2023; 18(2):550-567.
PMID: 37067674 PMC: 11014809. DOI: 10.1007/s12072-023-10516-x.
Wang J, Zheng Z, Wu T, Li W, Wang J, Pan Y J Hepatocell Carcinoma. 2022; 9:999-1010.
PMID: 36132426 PMC: 9483136. DOI: 10.2147/JHC.S379326.