Cost-effectiveness of tislelizumab plus chemotherapy vs chemotherapy as first-line treatment of PD-L1 positive advanced gastric or gastroesophageal junction adenocarcinoma from a Chinese perspective

Expert Rev Gastroenterol Hepatol. 2024 Jun;18(6):293-301. doi: 10.1080/17474124.2024.2373730. Epub 2024 Jun 28.

Abstract

Background: This work was designed to assess the cost-effectiveness of front-line tislelizumab plus chemotherapy (TIS+Chemo) in advanced gastric cancer (GC) or gastroesophageal junction cancer (GEJC) with positive expression of programmed cell death ligand 1 (PD-L1) from the perspective of Chinese healthcare system.

Research design and methods: A 10-year partitioned survival model was undertaken utilizing clinical data from RATIONALE 305. Costs and utilities were both discounted at an annual rate of 5%. The primary outcome was incremental cost-effectiveness ratios (ICERs) and calculated as the cost per quality-adjusted life years (QALYs). The willingness-to-pay (WTP) threshold was set as $18,625/QALY. Only direct medical costs were considered. Sensitivity analyses and subgroup analyses were performed to evaluate the robustness of the model.

Results: In the base-case analysis, the incremental cost and effectiveness associated with TIS+Chemo vs Chemo was 7,361 and 0.38 QALYs, respectively, leading to an ICER of 19,371/QALY. At the WTP threshold of $18,625/QALY, the TIS+Chemo was not a cost-effective first-line treatment option. The model outcomes were robust.

Conclusions: TIS+Chemo did not provide a cost-effective approach for PD-L1 positive advanced GC/GEJC in China setting. However, TIS+Chemo might be cost-effective in provinces with higher WTP threshold.

Clinical trial registration: RATIONALE 305, www.clinicaltrials.gov, identifier is NCT03777657.

Keywords: Cost-effectiveness analysis; GC/GEJC; RATIONALE 305; china; immunotherapy; tislelizumab.

Publication types

  • Comparative Study

MeSH terms

  • Adenocarcinoma* / drug therapy
  • Adenocarcinoma* / economics
  • Adenocarcinoma* / pathology
  • Aged
  • Antibodies, Monoclonal, Humanized* / economics
  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols* / economics
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • B7-H1 Antigen* / metabolism
  • China
  • Cost-Benefit Analysis*
  • Drug Costs
  • Esophageal Neoplasms* / drug therapy
  • Esophageal Neoplasms* / economics
  • Esophageal Neoplasms* / pathology
  • Esophagogastric Junction* / pathology
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / economics
  • Immune Checkpoint Inhibitors / therapeutic use
  • Male
  • Middle Aged
  • Models, Economic
  • Quality-Adjusted Life Years*
  • Stomach Neoplasms* / drug therapy
  • Stomach Neoplasms* / economics
  • Stomach Neoplasms* / pathology
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal, Humanized
  • B7-H1 Antigen
  • tislelizumab
  • CD274 protein, human
  • Immune Checkpoint Inhibitors

Associated data

  • ClinicalTrials.gov/NCT03777657