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Poster session 04

446P - CDK4/6 inhibitors in the first-line treatment of postmenopausal women with HR+/HER2- advanced or metastatic breast cancer: An updated network meta-analysis and cost-effectiveness analysis

Date

21 Oct 2023

Session

Poster session 04

Topics

Tumour Site

Breast Cancer

Presenters

Ni Zeng

Citation

Annals of Oncology (2023) 34 (suppl_2): S334-S390. 10.1016/S0923-7534(23)01260-7

Authors

N. Zeng1, J. Han2

Author affiliations

  • 1 Department Of Head And Neck Oncology, West China Medical Center of Sichuan University, 610041 - Chengdu/CN
  • 2 Department Of Oncology, West China School of Medicine/West China Hospital of Sichuan University, 610041 - Chengdu/CN

Resources

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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.

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