# Real-World Clinical Outcomes of Trilaciclib for the Prevention of Myelosuppression in Patients with Esophageal Cancer Undergoing Chemotherapy

**Authors:** Hui Chen, Jingze Yan, Zeyuan Liu, Xiaolin Ge, Xinchen Sun, Xiaojie Xia

PMC · DOI: 10.3390/curroncol32040189 · Current Oncology · 2025-03-24

## TL;DR

This study shows that trilaciclib helps prevent severe blood cell drops in esophageal cancer patients during chemotherapy, especially when used early.

## Contribution

The first demonstration of trilaciclib's effectiveness in preventing myelosuppression in esophageal cancer patients.

## Key findings

- Primary prevention with trilaciclib reduced severe myelosuppression compared to secondary prevention.
- The PP group had significantly fewer grade III/IV neutropenia and leukopenia events.
- Non-hematological toxicities and treatment efficacy were similar between groups.

## Abstract

This study aims to evaluate the clinical effectiveness of trilaciclib in preventing myelosuppression in patients with esophageal cancer undergoing chemotherapy. Based on the use of trilaciclib, 81 patients were divided into a primary prevention group (PP group, n = 49) and a secondary prevention group (SP group, n = 32). The incidence of myelosuppression, antibiotic usage rate, survival outcomes, and other treatment-related toxicities were analyzed using chi-square tests and Kaplan–Meier survival curves. The incidence of chemotherapy-induced myelosuppression in the SP group was significantly higher than that in the PP group (96.9% vs. 79.6%), with a significantly higher proportion of grade III and above events (37.6% vs. 8.2%, p < 0.05). For chemotherapy-induced neutropenia, the incidence of grade III/IV events in the SP group was significantly higher than in the PP group (28.1% vs. 8.2%, p = 0.017). Additionally, the SP group experienced higher rates and severity of chemotherapy-induced anemia and thrombocytopenia. The PP group provided better protection against grade III/IV leukopenia and neutropenia (p < 0.05). Non-hematological toxicities and efficacy outcomes were similar between groups (p > 0.05). The study is the first to demonstrate that trilaciclib is a safe and effective option for the prevention of myelosuppression in esophageal cancer patients.

## Linked entities

- **Chemicals:** trilaciclib (PubChem CID 68029831)
- **Diseases:** esophageal cancer (MONDO:0007576)

## Full-text entities

- **Diseases:** thrombocytopenia (MESH:D013921), leukopenia (MESH:D007970), neutropenia (MESH:D009503), toxicities (MESH:D064420), grade III (MESH:D001254), anemia (MESH:D000740), Esophageal Cancer (MESH:D004938)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12025781/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12025781/full.md

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Source: https://tomesphere.com/paper/PMC12025781