An Epidemiology Model for Estimating the Numbers of US Patients With Multiple Myeloma by Line of Therapy and Treatment Exposure.


Journal

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
ISSN: 1524-4733
Titre abrégé: Value Health
Pays: United States
ID NLM: 100883818

Informations de publication

Date de publication:
12 2022
Historique:
received: 26 07 2021
revised: 09 03 2022
accepted: 04 05 2022
pubmed: 14 8 2022
medline: 18 11 2022
entrez: 13 8 2022
Statut: ppublish

Résumé

Estimates on the distribution of patients with multiple myeloma (MM) by line of therapy (LOT) are scarce and get outdated quickly as new treatments become available. The objective of this study was to estimate the number of patients with MM by LOT and the number of patients who have received at least 4 previous LOTs including proteasome inhibitors, immunomodulatory agents, and anti-CD38 monoclonal antibodies (mAbs). A compartmental model was developed to calculate the number of patients by LOT. Two pathways were considered based on stem cell transplant eligibility, and at each pathway, treatments were stratified in 2 types: anti-CD38 mAbs or other. The model population was stratified into 4 subgroups based on age and cytogenetic risk. Model inputs were informed from real-world evidence. The model estimated that, in 2020, 126 869 patients were living with MM in the United States. Of these, 105 701 received treatment in any LOT, with 56 959, 27 252, 11 258, and 5217 in lines 1 to 4, respectively, and 5015 in line 5 or beyond. The model estimated that 3497 patients received at least 4 previous LOTs including proteasome inhibitors, immunomodulatory agents, and anti-CD38 mAbs. The model overall prevalence predictions aligned well with publicly available estimates. This study proposes a novel framework to estimate MM prevalence. It can assist clinicians to understand future trends in MM epidemiology, healthcare systems to plan for future resource use allocation, and payers to quantify the budget impact of new treatments.

Identifiants

pubmed: 35963840
pii: S1098-3015(22)01999-4
doi: 10.1016/j.jval.2022.05.011
pii:
doi:

Substances chimiques

Proteasome Inhibitors 0
Antineoplastic Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1977-1985

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Andreas Nikolaou (A)

Modelling and Simulation, Evidera, London, England, UK. Electronic address: a.nikolaou1986@gmail.com.

Cosmina Hogea (C)

Value Evidence and Outcomes, GlaxoSmithKline, Upper Providence, PA, USA.

Yevgeniy Samyshkin (Y)

Value Evidence and Outcomes, GlaxoSmithKline, Brentford, Middlesex, England, UK.

Eric M Maiese (EM)

Value Evidence and Outcomes, GlaxoSmithKline, Philadelphia, PA, USA.

Leah Sansbury (L)

Value Evidence and Outcomes, GlaxoSmithKline, Research Triangle Park, NC, USA.

Mustafa Oguz (M)

Real-World Evidence, Evidera, London, England, UK.

Javier Cid-Ruzafa (J)

Real-World Evidence, Evidera, Barcelona, Spain.

Ritika Kapoor (R)

Modelling and Simulation, Evidera, London, England, UK.

Feng Wang (F)

Value Evidence and Outcomes, GlaxoSmithKline, Upper Providence, PA, USA.

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Classifications MeSH