# Real-world experience with first-line pembrolizumab plus chemotherapy in Vietnamese patients with stage IV esophageal squamous cell carcinoma

**Authors:** Thuan Van Tran, Phuong Thu Nguyen, Quang Van Le, Giang Huong T. Nguyen, Huy Le Trinh, Kien Hoang Le, Giap Ngoc Hoang

PMC · DOI: 10.3389/fimmu.2026.1713860 · 2026-02-25

## TL;DR

This study examines how pembrolizumab plus chemotherapy works in Vietnamese patients with advanced esophageal cancer, finding it has a manageable safety profile and similar recurrence patterns to international reports.

## Contribution

The study provides real-world evidence from Vietnam on pembrolizumab plus chemotherapy for stage IV ESCC, a treatment previously only supported by clinical trials.

## Key findings

- Pembrolizumab plus chemotherapy had a manageable safety profile in Vietnamese patients with stage IV ESCC.
- Lymph node progression was the most common site of disease recurrence.
- Hematologic toxicities like neutropenia and anemia were frequently observed.

## Abstract

Esophageal squamous cell carcinoma (ESCC) remains a major cause of cancer-related mortality in Asia. Pembrolizumab in combination with chemotherapy has become a standard first-line option based on phase III trial data, but real-world evidence from Vietnam is lacking. This study examined the clinical characteristics, disease course, and treatment-related toxicities of Vietnamese patients with stage IV ESCC receiving this regimen.

We conducted a single-center, single-arm, retrospective analysis of 53 patients with stage IV ESCC treated with pembrolizumab plus platinum- and fluoropyrimidine-based chemotherapy. Information on demographics, clinical presentation, pathology, biomarker status, treatment regimens, patterns of progression or recurrence, and adverse events (AEs) was collected from electronic health records.

The mean age was 59 years, with nearly all patients being male. Most presented with advanced T3/N2 disease and dysphagia at diagnosis. PD-L1 status was unavailable in about one-third of cases. Common chemotherapy backbones were CF (50.9%) and XELOX/SOX (24.5%). Progression or recurrence was documented in 24.5% of patients, and 20.8% occurred within six months. Lymph nodes were the most frequent site of progression, followed by local and distant recurrence. Hematologic toxicities were common, including neutropenia (43.4% all grades, 13.2% grade ≥3) and anemia (50.9% all grades). Nausea (20.8%) and diarrhea (5.7%) were the main gastrointestinal toxicities. Immune-related events included hypothyroidism (3.8%) and pneumonitis (3.8%).

In this Vietnamese cohort, pembrolizumab plus chemotherapy showed a manageable safety profile and recurrence patterns consistent with those reported internationally. These findings add region-specific real-world evidence and underline the importance of broader multi-center studies with longer follow-up to inform practice in advanced ESCC.

## Linked entities

- **Chemicals:** platinum (PubChem CID 23939), fluoropyrimidine (PubChem CID 141643), nausea (PubChem CID 23963)
- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** pneumonitis (MESH:D011014), diarrhea (MESH:D003967), Nausea (MESH:D009325), ESCC (MESH:D000077277), cancer (MESH:D009369), disease (MESH:D004194), IV (MESH:D006011), toxicities (MESH:D064420), gastrointestinal toxicities (MESH:D005767), hypothyroidism (MESH:D007037), neutropenia (MESH:D009503), Hematologic toxicities (MESH:D006402), dysphagia (MESH:D003680), anemia (MESH:D000740)
- **Chemicals:** platinum (MESH:D010984), XELOX (MESH:C519688), Pembrolizumab (MESH:C582435), CF (MESH:D002142), SOX (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12975916/full.md

---
Source: https://tomesphere.com/paper/PMC12975916