Cost-effectiveness analysis of pembrolizumab plus chemotherapy as first-line therapy for extensive-stage small-cell lung cancer

PLoS One. 2021 Nov 15;16(11):e0258605. doi: 10.1371/journal.pone.0258605. eCollection 2021.

Abstract

Background: The phase III KEYNOTE-604 study confirmed the benefit of pembrolizumab combined with chemotherapy in the first-line treatment of extensive-stage small-cell lung cancer (ES-SCLC). Taken into account the clinical benefits of pembrolizumab and its high cost, this study aimed to assess the cost-effectiveness of adding pembrolizumab to standard first-line etoposide-platinum (EP) for patients with ES-SCLC from the US payer perspective.

Methods: A Markov model was developed to compare the cost and quality-adjusted life-year (QALY) of pembrolizumab plus EP and placebo plus EP over a 10-year time horizon. Clinical efficacy and safety data were pooled from the KEYNOTE-604 trial. Utilities were obtained from published resources. Costs were mainly collected from Medicare in 2020. Sensitivity analyses were performed to examine the robustness of our model.

Results: Adding pembrolizumab to standard first-line EP resulted in the better effectiveness than EP chemotherapy alone for ES-SCLC by 0.22 QALYs. Pembrolizumab plus EP was dominated economically by placebo plus EP, leading to an incremental cost-effectiveness ratio (ICER) of $334,373/ QALY. Deterministic sensitivity analyses indicated that the uncertainty in model parameters exerted no substantial effect on our results. Probability sensitivity analysis indicated that probabilities for pembrolizumab plus EP being cost-effective within a wide range of willingness to pay were modest.

Conclusion: From the US payer perspective, the first-line treatment for ES-SCLC with pembrolizumab plus EP was not cost-effective compared with placebo plus EP. Although pembrolizumab combination chemotherapy was beneficial to the survival of ES-SCLC, price reduction may be the necessary to improve its cost-effectiveness.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal, Humanized / economics
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Antineoplastic Agents, Immunological / economics
  • Antineoplastic Agents, Immunological / therapeutic use*
  • Antineoplastic Agents, Phytogenic / economics
  • Antineoplastic Agents, Phytogenic / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / economics
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cost-Benefit Analysis / methods*
  • Double-Blind Method
  • Etoposide / economics
  • Etoposide / therapeutic use*
  • Follow-Up Studies
  • Humans
  • Immunotherapy / methods*
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / epidemiology
  • Lung Neoplasms / pathology
  • Markov Chains
  • Medicare
  • Neoplasm Staging
  • Platinum / therapeutic use*
  • Progression-Free Survival
  • Quality-Adjusted Life Years
  • Small Cell Lung Carcinoma / drug therapy*
  • Small Cell Lung Carcinoma / epidemiology
  • Small Cell Lung Carcinoma / pathology
  • United States / epidemiology

Substances

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents, Immunological
  • Antineoplastic Agents, Phytogenic
  • Platinum
  • Etoposide
  • pembrolizumab

Grants and funding

This work was supported by the Hunan Provincial Natural Science Foundation [grant numbers 2019JJ50864]; Scientific research project of Hunan Health Commission in 2019[grant numbers B2019156]. Qiao Liu received the funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.