TY - JOUR
T1 - Lifetime Costs for Treated Follicular Lymphoma Patients in the US
AU - Eichten, Caitlin
AU - Ma, Qiufei
AU - Delea, Thomas E.
AU - Hagiwara, May
AU - Ramos, Roberto
AU - Iorga, Şerban R.
AU - Zhang, Jie
AU - Maziarz, Richard T.
N1 - Funding Information:
TED is an employee and owner of PAI. PAI received research funding from Novartis for this study. CE and MH are employees of PAI. PAI received research funding from Novartis for this study. QM, RR, SRI, and JZ are employees of Novartis. Novartis provided research funding to PAI for this study. RTM: Honoraria, membership on an entity’s Board of Directors or advisory committees and research funding: Novartis; Consultancy and honoraria: Incyte, Juno; Honoraria: Kite, Jazz Pharmaceuticals; Patents & Royalties: Athersys, Inc.; Employment: Oregon Health & Science University (OHSU); with regard to the consultant services and payment from Novartis, this potential conflict of interest has been reviewed and managed by OHSU.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Switzerland AG.
PY - 2021/10
Y1 - 2021/10
N2 - Background and Objective: The objective of this study was to estimate the lifetime costs of patients receiving treatment for follicular lymphoma (FL) in the United States. Methods: A Markov model was programmed in hēRo3 with a 6-month cycle length, 35-year time horizon (lifetime projection), and health states for line of treatment, response, receipt of maintenance therapy among responders, transformation to diffuse large B-cell lymphoma (DLBCL), development of second primary malignancy (SPM), and death. The model was used to estimate the expected lifetime costs of FL (in 2019 USD), including costs of drug acquisition and administration, transplant procedures, radiotherapy, adverse events, follow-up, DLBCL, SPM, end-of-life care, and indirect costs. Model inputs were based on published sources. Results: In the US, patients with FL receiving treatment have a life expectancy of approximately 14.5 years from initiation of treatment and expected lifetime direct and indirect costs of US$515,884. Costs of drugs for induction therapy represent the largest expenditure (US$233,174), followed by maintenance therapy costs (US$88,971) and terminal care costs (US$57,065). Despite the relatively advanced age of these patients, indirect costs (due to patient morbidity and mortality and caregiver lost work time) represent a substantial share of total costs (US$40,280). Treated FL patients spend approximately 6.9 years in the health states associated with first-line therapy. Approximately 66 and 46% continue to second- and third-line therapies, respectively. The mean (95% credible interval) of expected lifetime costs based on the probabilistic sensitivity analyses was US$559,202 (421,997–762,553). Conclusions: In the US, the expected lifetime costs of care for FL patients who receive treatment is high. The results highlight the potential economic benefits that might be achieved by treatments for FL that prevent or delay disease progression.
AB - Background and Objective: The objective of this study was to estimate the lifetime costs of patients receiving treatment for follicular lymphoma (FL) in the United States. Methods: A Markov model was programmed in hēRo3 with a 6-month cycle length, 35-year time horizon (lifetime projection), and health states for line of treatment, response, receipt of maintenance therapy among responders, transformation to diffuse large B-cell lymphoma (DLBCL), development of second primary malignancy (SPM), and death. The model was used to estimate the expected lifetime costs of FL (in 2019 USD), including costs of drug acquisition and administration, transplant procedures, radiotherapy, adverse events, follow-up, DLBCL, SPM, end-of-life care, and indirect costs. Model inputs were based on published sources. Results: In the US, patients with FL receiving treatment have a life expectancy of approximately 14.5 years from initiation of treatment and expected lifetime direct and indirect costs of US$515,884. Costs of drugs for induction therapy represent the largest expenditure (US$233,174), followed by maintenance therapy costs (US$88,971) and terminal care costs (US$57,065). Despite the relatively advanced age of these patients, indirect costs (due to patient morbidity and mortality and caregiver lost work time) represent a substantial share of total costs (US$40,280). Treated FL patients spend approximately 6.9 years in the health states associated with first-line therapy. Approximately 66 and 46% continue to second- and third-line therapies, respectively. The mean (95% credible interval) of expected lifetime costs based on the probabilistic sensitivity analyses was US$559,202 (421,997–762,553). Conclusions: In the US, the expected lifetime costs of care for FL patients who receive treatment is high. The results highlight the potential economic benefits that might be achieved by treatments for FL that prevent or delay disease progression.
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U2 - 10.1007/s40273-021-01052-3
DO - 10.1007/s40273-021-01052-3
M3 - Article
C2 - 34273085
AN - SCOPUS:85110677424
SN - 1170-7690
VL - 39
SP - 1163
EP - 1183
JO - PharmacoEconomics
JF - PharmacoEconomics
IS - 10
ER -