# Tislelizumab efficacy and safety compared to other anti–PD-1s: a network meta-analysis of first-line therapies for unresectable, locally advanced or metastatic esophageal squamous cell carcinoma

**Authors:** Jaffer A. Ajani, Elizabeth Smyth, David Tougeron, Hyun Ae Jung, Wenxi Tang, Jason Steenkamp, Emily Prentiss, JeanPierre Coaquira Castro, Kirk Szafranski, Lin Zhan

PMC · DOI: 10.3389/fimmu.2025.1657085 · Frontiers in Immunology · 2026-01-06

## TL;DR

This study compares the effectiveness and safety of tislelizumab plus chemotherapy to other PD-1 inhibitors in treating advanced esophageal cancer.

## Contribution

A network meta-analysis comparing tislelizumab with other PD-1 inhibitors in first-line treatment for esophageal squamous cell carcinoma.

## Key findings

- Tislelizumab + chemotherapy showed similar overall survival but better progression-free survival compared to nivolumab + chemotherapy.
- Safety profiles of tislelizumab, nivolumab, and pembrolizumab were comparable in treating advanced ESCC.
- Tislelizumab + chemotherapy demonstrated comparable efficacy to pembrolizumab + chemotherapy across subgroups.

## Abstract

The addition of programmed cell death protein-1 (PD-1) inhibitors to chemotherapy (CT) or anti-CTLA4 (ipilimumab) has recently emerged as an effective first-line (1L) treatment for esophageal squamous cell carcinoma (ESCC), the most common form of esophageal cancer globally.

A systematic literature review (SLR) was conducted to identify randomized controlled trials (RCTs) investigating 1L PD-1 inhibitor regimens in adult patients with unresectable, locally advanced, or metastatic ESCC. Bayesian NMAs were conducted to evaluate overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and grade ≥3 treatment-related adverse events (TRAEs).

Three eligible RCTs were identified, evaluating three PD-1 inhibitor regimens with broad regulatory approval for 1L ESCC in combination with CT (tislelizumab, nivolumab, and pembrolizumab). Tislelizumab + CT demonstrated similar long-term OS to nivolumab + CT and pembrolizumab + CT but a significant PFS benefit over nivolumab + CT and comparable efficacy to pembrolizumab + CT. Subgroup analyses were consistent with the base case, including among patients with varying PD-L1 expression (≥1% and ≥5% Tumor Area Positivity [TAP] score or ≥1 and ≥5 combined positive score [CPS]), Asia versus the rest of world, and different underlying CT backbones. Safety profiles were comparable across the three treatments.

Tislelizumab + CT is an effective 1L treatment option for advanced or metastatic ESCC, demonstrating comparable efficacy and safety outcomes relative to existing treatments.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1), CTLA4 (cytotoxic T-lymphocyte associated protein 4)
- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580), esophageal cancer (MONDO:0007576)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** ESCC (MESH:D000077277), Tumor (MESH:D009369), esophageal cancer (MESH:D004938)
- **Chemicals:** pembrolizumab (MESH:C582435), nivolumab (MESH:D000077594), ipilimumab (MESH:D000074324), Tislelizumab (MESH:C000707970)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12816255/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12816255/full.md

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Source: https://tomesphere.com/paper/PMC12816255