# Immune repertoire sequencing reveals differences in treatment response to camrelizumab plus platinum-based chemotherapy in advanced ESCC

**Authors:** Xiaoling Zhang, Wenqi Zhao, Yunyi Du, Fei Su, Yuexiang Zhang, Hui Wang, Yongai Li, Min Liu, Yangjun Gao, Linlin Cai, Tingting Feng, Mei Wang, Chunmei Yao, Ning Xu, Yu Wang, Guohua Song, Wenqing Hu, Jun Zhao

PMC · DOI: 10.3389/fimmu.2025.1526443 · 2025-02-26

## TL;DR

This study shows that combining camrelizumab with chemotherapy is effective for advanced esophageal cancer, and immune sequencing reveals differences in immune responses between responders and non-responders.

## Contribution

The study introduces immune repertoire sequencing as a tool to understand treatment response mechanisms in ESCC patients receiving camrelizumab plus chemotherapy.

## Key findings

- Camrelizumab plus chemotherapy achieved a 64.8% objective response rate in advanced ESCC patients.
- Immune repertoire sequencing revealed significant differences in TCR and BCR CDR3 sequences between responders and non-responders.
- Oligoclonal enrichment and specific V/J gene abundance differences were observed in TCR and BCR between groups.

## Abstract

This study evaluated the efficacy and safety of camrelizumab combined with platinum-based chemotherapy (taxanes [T] or fluorouracil agents [F] plus platinum [P] drugs) as the first-line treatment in advanced esophageal squamous cell carcinoma (ESCC), using immune repertoire sequencing (IRS) to explore treatment response mechanism. In this multi-center, prospective cohort study, 88 patients received camrelizumab plus TP or FP, achieving a 1-year progression-free survival of 56.8% and overall survival of 68.2%. The objective response rate (ORR) was 64.8%, with a disease control rate of 91.1%. While most treatment-related adverse events were mild, 12.5% of patients experienced grade ≥3 toxicities. IRS showed significant differences in T-cell receptor (TCR) β-chain and immunoglobulin heavy chain between patients with (ORR group) or without ORR (non-ORR group), particularly in the distribution and expression of some genes. Specifically, we found the significant differences in the amino acid composition of complementarity determining region 3 (CDR3) polypeptide sequences in TCR and B-cell receptor (BCR) between the ORR and non-ORR groups. For TCR, we observed substantial oligoclonal enrichment and differences in the abundance of specific V and J genes. Similarly, for BCR, we detected differences in the clonotype abundance of CDR3 polypeptide segments and identified several differential V genes. Camrelizumab combined with platinum-based chemotherapy is effective and well-tolerated as the first-line treatment for ESCC, and IRS may reveal mechanism influencing treatment response.

## Linked entities

- **Chemicals:** taxanes (PubChem CID 78384800), platinum (PubChem CID 23939)
- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580)

## Full-text entities

- **Genes:** IGHD (immunoglobulin heavy constant delta) [NCBI Gene 3495]
- **Diseases:** ESCC (MESH:D000077277), toxicities (MESH:D064420)
- **Chemicals:** Camrelizumab (MESH:C000631724), platinum (MESH:D010984), taxanes (MESH:D043823), fluorouracil (MESH:D005472)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11897899/full.md

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Source: https://tomesphere.com/paper/PMC11897899