TY - JOUR
T1 - Economic burden of disease progression among multiple myeloma patients who have received transplant and at least one line of therapy in the US
AU - Fonseca, Rafael
AU - Hagiwara, May
AU - Panjabi, Sumeet
AU - Yucel, Emre
AU - Buchanan, Jacqueline
AU - Delea, Thomas
N1 - Funding Information:
Funding for this study was provided to Policy Analysis Inc. by Amgen Inc. The manuscript was funded by Amgen Inc. Sumeet Panjabi, Emre Yucel, and Jacqueline Buchanan are employees of and own stock options in Amgen Inc. I am an employee of Policy Analysis Inc. (PAI) and T.E.D. is a partner at Policy Analysis Inc. (PAI), who has received research funding from Amgen Inc. for this and other studies. R.F. practices medicine at Mayo Clinic and is a consultant for Amgen.
Funding Information:
J.B. is currently an employee of Amgen, Inc. and S.P. and E.Y. were employees of Amgen, Inc. and all hold Amgen Stock. R.F. is a consultant for Amgen, BMS, Celgene, Takeda, Bayer, Janssen, Novartis, Pharmacyclics, Sanofi, Merck, Juno, Kite, Aduro, OncoTracker, Oncopeptides, GSK, and AbbVie, and is on the Scientific Advisory Board of Adaptive Biotechnologies and OncoTracker. M.H. and T.E.D. received research funding from Amgen, Celgene, EMD Serono, Jazz, Merck, Novartis, Pfizer, Sanofi, Seattle Genetics, and Takeda.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/2
Y1 - 2021/2
N2 - Effects of disease progression on healthcare resource utilization (HRU) and costs among multiple myeloma (MM) patients with ≥1 line of therapy (LOT) who received their first stem cell transplant (SCT) within 1 year of initial MM diagnosis were estimated using a large US claims database. Disease progression was defined as advancement to the next LOT, bone metastasis, hypercalcemia, soft tissue plasmacytoma, skeletal related events, acute kidney disease, or death within 12 months of LOT initiation. Annual HRU and costs in the first three LOTs (L1–L3) were compared for patients with versus without disease progression using inverse probability of treatment weighting to adjust for differences between groups in baseline characteristics. In all LOTs, mean annual hospitalizations and healthcare costs were greater for patients with versus without progression. Total incremental annual costs among patients with versus without progression in L1–L3 were $18,359, $87,055, and $71,917, respectively, among LOTs initiated between 2006 and 2018. In LOTs initiated between 2013 and 2018, the figures were $46,024, $100,329, and $101,942 in L1–L3, respectively. The economic burden of disease progression is substantial in this population of MM patients who underwent SCT and received systemic anti-myeloma therapy.
AB - Effects of disease progression on healthcare resource utilization (HRU) and costs among multiple myeloma (MM) patients with ≥1 line of therapy (LOT) who received their first stem cell transplant (SCT) within 1 year of initial MM diagnosis were estimated using a large US claims database. Disease progression was defined as advancement to the next LOT, bone metastasis, hypercalcemia, soft tissue plasmacytoma, skeletal related events, acute kidney disease, or death within 12 months of LOT initiation. Annual HRU and costs in the first three LOTs (L1–L3) were compared for patients with versus without disease progression using inverse probability of treatment weighting to adjust for differences between groups in baseline characteristics. In all LOTs, mean annual hospitalizations and healthcare costs were greater for patients with versus without progression. Total incremental annual costs among patients with versus without progression in L1–L3 were $18,359, $87,055, and $71,917, respectively, among LOTs initiated between 2006 and 2018. In LOTs initiated between 2013 and 2018, the figures were $46,024, $100,329, and $101,942 in L1–L3, respectively. The economic burden of disease progression is substantial in this population of MM patients who underwent SCT and received systemic anti-myeloma therapy.
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U2 - 10.1038/s41408-021-00431-5
DO - 10.1038/s41408-021-00431-5
M3 - Article
C2 - 33941766
AN - SCOPUS:85105216879
SN - 2044-5385
VL - 11
JO - Blood Cancer Journal
JF - Blood Cancer Journal
IS - 2
M1 - 35
ER -