# Feasibility of systemic therapy in unresectable gastric/gastroesophageal junction cancer with overt bleeding

**Authors:** Yanhong Yao, Zhentao Liu, Hua Zhang, Xinhua Shi, Fangfang Huang, Yi Zhang, Lu Chen, Yanyan Shi, Baoshan Cao

PMC · DOI: 10.1016/j.apjon.2025.100750 · Asia-Pacific Journal of Oncology Nursing · 2025-07-07

## TL;DR

This study shows that modified cancer treatments can be safely used in patients with advanced stomach or esophagus cancer who are bleeding, with good response and survival rates.

## Contribution

The study demonstrates the feasibility of modified systemic therapy in a high-risk cancer population with active bleeding.

## Key findings

- Modified systemic therapy achieved a 42.3% response rate and 90.4% disease control in patients with bleeding GC/GEJC.
- 28.8% of patients experienced persistent bleeding after treatment, linked to worse survival outcomes.
- Dose reductions and careful hemostasis management enabled treatment in this high-risk group.

## Abstract

To evaluate the feasibility of modified systemic anti-cancer therapy in unresectable gastric cancer or gastroesophageal junction cancer (GC/GEJC) patients with overt bleeding (OB).

This retrospective study included individuals with unresectable GC/GEJC and OB who received systemic anti-cancer therapy. Treatment feasibility was assessed. Risk factors for persistent overt bleeding post systemic therapy (POBPST) were explored.

Among the 52 individuals included, 19 (36.5%) experienced active OB within one month prior to initiating anti-cancer therapy, while 33 (63.5%) did not. Hemostasis was achieved via endoscopic intervention in 2 patients and conservative medical management in 17. A total of 5 patients received immune checkpoint inhibitor monotherapy, and 47 received chemotherapy-based systemic therapy, with 70.2% (33/47) requiring a 25% dose reduction. Among those with active OB, 73.7% (14/19) received intravenous therapy, with a median interval of 16 days (range: 3–25) from hemostasis to treatment initiation. The overall objective response rate (ORR) and disease control rate (DCR) were 42.3% and 90.4%, respectively. Median progression-free survival (mPFS) and overall survival (mOS) were 10.3 and 16.1 months. POBPST occurred in 28.8% of individuals and was associated with poorer survival. Grade 3–4 treatment-related adverse events occurred in 36.5% of patients. Multivariate analysis identified a Modified Barthel Index (MBI) score < 75 and disease progression or stable disease as independent risk factors for POBPST.

With appropriate hemostatic management, modified dose systemic anti-cancer therapy was feasible and generally well tolerated in patients with unresectable GC/GEJC and OB. Nurses’ role was indispensable for this high-risk population.

The study has been registered in clinical trials.gov (NCT06522542).

## Linked entities

- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}
- **Diseases:** PR (MESH:D004828), cardiac dysfunction (MESH:D006331), Hemorrhage (MESH:D006470), MMR-deficient (MESH:C536928), Morse Fall (MESH:C537863), SD (MESH:D060050), POBPST (MESH:D000094025), hematological toxicity (MESH:D006402), HAD (MESH:C535310), GEJC (MESH:D009369), adenocarcinoma (MESH:D000230), signet-ring carcinoma (MESH:D018279), GC (MESH:D013274), hematochezia (MESH:D006471), death (MESH:D003643), IV (MESH:D006011), melena (MESH:D008551), malnutrition (MESH:D044342), hematemesis (MESH:D006396), Anti (MESH:D006679), PD (MESH:D018450), allergy (MESH:D004342), lung squamous cell carcinoma (MESH:D002294), circulatory failure (MESH:D012769), lung metastasis (MESH:D009362), retroperitoneal lymph node metastasis (MESH:D008207), gastrointestinal reaction (MESH:D005767), anemia (MESH:D000740)
- **Chemicals:** trastuzumab (MESH:D000068878), fluorouracil (MESH:D005472), S-1 (-), DCS (MESH:D003523), DS (MESH:D003903), urea nitrogen (MESH:C530477), pembrolizumab (MESH:C582435), sintilimab (MESH:C000632826)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310399/full.md

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Source: https://tomesphere.com/paper/PMC12310399