Abstract 446P
Background
Recently updated results of clinical trials have confirmed that palbociclib, ribociclib and abemaciclib plus letrozole/anastrozole significantly prolonged survival compared to placebo plus letrozole/anastrozole in the first-line treatment for postmenopausal women with HR+/HER2- metastatic breast cancer. However, the high cost of CDK4/6 inhibitors imposes a huge financial burden on patients and healthcare systems.
Methods
Studies estimating CDK4/6 inhibitors plus NSAI for HR+/HER2- ABC were searched. A network meta-analysis was made with the main outcomes HRs of OS and PFS. The costs and efficacy of four first-line therapies for HR+/HER2- ABC were evaluated by Markov model. The main outcomes in the cost-effectiveness analysis were incremental cost-utility ratios (ICURs), incremental monetary benefit (INMB), and incremental net-health benefit (INHB). The robustness of the model was assessed by one-way, three-way, and probabilistic sensitivity analyses.
Results
Seven studies involving 5347 patients were included in the NMA. The three first-line CDK4/6 inhibitors plus NSAI groups provided significant PFS and OS superiority to NSAI alone. Abem+NSAI represented a significant statistical advantage on PFS and indicated a trend in best OS benefit compared to the Placebo+NSAI group. Abem+NSAI, Palbo+NSAI, and Ribo+NSAI groups resulted in additional costs of $12,602, $20,391, and $81,258, with additional effects of 0.38, 0.31, and 0.30 QALYs, respectively, leading to an ICUR of $33,163/QALY, $65,777/QALY, and $270,860/QALY. Additional pairwise comparisons showed Abem+NSAI was the only cost-effective option in three CDK4/6 inhibitors plus NSAI groups. The sensitivity analyses showed that the proportion of receiving subsequent CDK4/6 inhibitors and the cost of abemaciclib significantly influenced the results of Abem+NSAI.
Conclusions
From the Chinese payers'perspective, Abem+NSAI was a cost-effective treatment compared with Placebo+NSAI at the willingness-to-pay of $38,029/QALY. The Palbo+NSAI and Ribo+NSAI groups were cost-effective unless adjusting drug prices to 50% or 10% of current prices is probably cost-effective.
Clinical trial identification
CRD42023399342.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
457P - Disparities in receipt of CDK4/6 inhibitors with endocrine therapy as therapy for hormone receptor-positive, HER2-negative metastatic breast cancer in the real-world setting
Presenter: Gretchen Kimmick
Session: Poster session 04
458P - Metastatic breast cancer: How and how often do we communicate? Results from an Italian national survey
Presenter: Camilla Lisanti
Session: Poster session 04
460P - Impact of fulvestrant utilization on prognostic outcome among patients with HR+ve/HER2-ve metastatic breast cancer: Results from a real-world dataset
Presenter: Shaheenah Dawood
Session: Poster session 04
462P - Health outcomes of treatment sequences with eribulin or other single agents’ chemotherapy for treating relapsed metastatic HER2-negative breast cancer
Presenter: Simone Rivolo
Session: Poster session 04
463P - Impact of two waves of Sars-Cov-2 outbreak on the clinical presentation and outcomes of newly referred breast cancer cases at AP-HP: A retrospective multicenter cohort study
Presenter: Sonia Priou
Session: Poster session 04
464P - Developing a prognostic risk stratification model and treatment options for HER2-positive breast cancer brain metastasis
Presenter: JiaXin Chen
Session: Poster session 04
465P - Reporting of older subgroups enrolled to registration breast cancer trials, 2012-2021
Presenter: Colm Mac Eochagain
Session: Poster session 04
466P - Integrated analysis of potential prognosis and differential expression between primary and metastatic foci for COL12A1 in breast cancer
Presenter: Lei Tang
Session: Poster session 04