# A cost-effectiveness analysis comparing pembrolizumab combined with chemotherapy versus chemotherapy alone for advanced biliary tract cancer: US and China perspectives

**Authors:** Chunhua Zhang, Hua Liang, Yanni Qin, Xiaolan Tan, Xiaoqing Su, Xin Tian, Yumei Nong

PMC · DOI: 10.1371/journal.pone.0341154 · PLOS One · 2026-01-22

## TL;DR

This study compares the cost-effectiveness of pembrolizumab plus chemotherapy versus chemotherapy alone for advanced biliary tract cancer in the US and China.

## Contribution

The study provides a novel cost-effectiveness analysis of pembrolizumab plus chemotherapy for biliary tract cancer from both US and Chinese payer perspectives.

## Key findings

- Pembrolizumab plus chemotherapy is not cost-effective in China at the tested willingness-to-pay thresholds.
- In the US, the treatment yields a small gain in quality-adjusted life years but is not cost-effective.
- Subgroup analyses suggest better survival subgroups may benefit more from the treatment.

## Abstract

In the KEYNOTE-966 study, the clinical benefits of pembrolizumab plus chemotherapy were demonstrated for patients with advanced biliary tract cancer (BTC). At this point, it is unknown whether this expensive therapy is cost-effective. The purpose of this study was to evaluate the cost-effectiveness of pembrolizumab plus chemotherapy in treating BTC.

We constructed a partitioned survival model form the perspectives of US and Chinese payers. KEYNOTE-966 was used to obtain the baseline characteristics of the patients as well as their clinical data. Local databases and published literature were used to collect costs and utilities. Costs, life years, quality-adjusted life years (QALYs), incremental cost-effectiveness ratios (ICERs), incremental net health benefits (INHB), and incremental net monetary benefits (INMB) were measured and compared. We conducted sensitivity analyses in order to assess the robustness of the model. Subgroup analyses were also performed.

Pembrolizumab plus chemotherapy is not cost-effective in China at the willingness to pay (WTP) thresholds of $38,258 and $84,866. However, it yielded an additional 0.137 QALYs and an additional $63,864 (ICER $466,340) over chemotherapy alone. In the US, this treatment was not cost-effective, resulting in an improvement in effectiveness of 0.144 QALYs and an increase in overall cost of $141,000 (ICER of $976,925). There were INHBs of −0.616 QALYs and INMBs of -$52,237 for pembrolizumab plus chemotherapy in China if the WTP threshold for QALYs was set at $84,866, and INHBs of −0.796 QALYs and INMBs of -$119,400 when the WTP threshold was set at $150,000 for the US. Through sensitivity analyses, it was demonstrated that the results were stable. The results of the subgroup analysis indicate that better survival properties subgroups were more likely to be cost-effective, although pembrolizumab plus chemotherapy may not be cost-effective for all subgroups.

In the US and China, pembrolizumab plus chemotherapy may not be a cost-effective treatment option. This study provides evidence-based pricing strategies that may benefit decision makers and clinicians as they make clinical decisions. For a better understanding of the impact on budgets and the affordability of care for patients, more evidence is required.

## Linked entities

- **Diseases:** biliary tract cancer (MONDO:0003060)

## Full-text entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, FGFR2 (fibroblast growth factor receptor 2) [NCBI Gene 2263] {aka BBDS, BEK, BFR-1, CD332, CEK3, CFD1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, PLAG1 (PLAG1 zinc finger) [NCBI Gene 5324] {aka PSA, SGPA, SRS4, ZNF912}
- **Diseases:** anemia (MESH:D000740), chronic viral hepatitis (MESH:D006525), fatigue (MESH:D005221), cancers of the intrahepatic or extrahepatic bile ducts (MESH:D001650), toxicity (MESH:D064420), cholangiocarcinoma (MESH:D018281), death (MESH:D003643), OS (MESH:D011475), thrombocytopenia (MESH:D013921), inflammatory (MESH:D007249), gallbladder cancer (MESH:D005706), productivity loss (MESH:D007787), Tumors (MESH:D009369), hepatocellular carcinoma (MESH:D006528), biliary tract injuries (MESH:D001660), cirrhosis (MESH:D005355), gastrointestinal malignancies (MESH:D005770), neutrophilia (MESH:C563010), PD (MESH:D018450), BTC (MESH:D001661), asthenia (MESH:D001247)
- **Chemicals:** paclitaxel (MESH:D017239), cisplatin (MESH:D002945), gemcitabine (MESH:D000093542), fluorouracil (MESH:D005472), Pembrolizumab (MESH:C582435), KEYNOTE- (-), carboplatin (MESH:D016190), durvalumab (MESH:C000613593)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12826477/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12826477/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12826477/full.md

---
Source: https://tomesphere.com/paper/PMC12826477