Trilaciclib and the economic value of multilineage myeloprotection from chemotherapy-induced myelosuppression among patients with extensive-stage small cell lung cancer treated with first-line chemotherapy.

Anemia I I00 I1 I10 chemotherapy-induced myelosuppression economic evaluation neutropenia quality of life thrombocytopenia trilaciclib

Journal

Journal of medical economics
ISSN: 1941-837X
Titre abrégé: J Med Econ
Pays: England
ID NLM: 9892255

Informations de publication

Date de publication:
Nov 2021
Historique:
pubmed: 8 12 2021
medline: 22 12 2021
entrez: 7 12 2021
Statut: ppublish

Résumé

Proliferating hematopoietic stem and progenitor cells (HSPCs) are susceptible to chemotherapy-induced damage, resulting in myelosuppressive adverse events (AEs) such as neutropenia, anemia, and thrombocytopenia that are associated with high health care costs and decreased quality of life (QoL). In this study, a trial-based cost-effectiveness analysis was performed to help assess the economic impact of administering trilaciclib, a myeloprotective therapy that protects multilineage HSPCs from chemotherapy-induced damage, prior to standard first-line chemotherapy, using data from a pivotal Phase II study of trilaciclib in the setting of extensive-stage small cell lung cancer (ES-SCLC, NCT03041311). The aim of this study was to assess the cost-effectiveness of administering trilaciclib prior to chemotherapy versus chemotherapy alone among patients with ES-SCLC from a United States payer perspective. Data on the rate and frequency of myelosuppressive AEs and health utility were derived from the pivotal study of trilaciclib. Costs of managing myelosuppressive AEs and costs of chemotherapy treatment were sourced from published literature. Outcomes included the number of myelosuppressive AEs, costs (in 2021 US dollars), quality-adjusted life-years (QALYs), incremental cost, incremental QALY, and an incremental cost-effectiveness ratio. Administering trilaciclib prior to chemotherapy was associated with a reduction in neutropenia (82%), febrile neutropenia (75%), anemia (43%), and thrombocytopenia (96%) compared with chemotherapy alone. Additionally, trilaciclib prior to chemotherapy was cost-saving compared with chemotherapy alone ($99,919 vs $118,759, respectively) and associated with QALY improvement (0.150 vs 0.145, respectively). Probabilistic sensitivity analyses showed 58% of iterations projecting cost savings and QALY improvement with trilaciclib. The findings suggest that the use of trilaciclib prior to first-line chemotherapy in patients with ES-SCLC can be cost-beneficial owing to fewer myelosuppressive AEs and lower costs, together with a favorable QoL profile.

Identifiants

pubmed: 34873975
doi: 10.1080/13696998.2021.2014163
doi:

Substances chimiques

Antineoplastic Agents 0
Pyrimidines 0
Pyrroles 0
trilaciclib U6072DO9XG

Banques de données

ClinicalTrials.gov
['NCT03041311']

Types de publication

Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

71-83

Auteurs

Ivo Abraham (I)

Center for Health Outcomes and PharmacoEconomic Research, University of Arizona, Tucson, AZ, USA.
Department of Pharmacy Practice and Science, College of Pharmacy, University of Arizona, Tucson, AZ, USA.
University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.
Matrix45, Tucson, AZ, USA.

Uchenna Onyekwere (U)

ZS Associates, Evanston, IL, USA.

Baris Deniz (B)

ZS Associates, Evanston, IL, USA.

Donald Moran (D)

G1 Therapeutics, Inc., Research Triangle Park, NC, USA.

Marc Chioda (M)

G1 Therapeutics, Inc., Research Triangle Park, NC, USA.

Huan Huang (H)

G1 Therapeutics, Inc., Research Triangle Park, NC, USA.

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Classifications MeSH