# Efficacy and safety of nanoparticle albumin-bound paclitaxel plus cisplatin or nedaplatin plus tegafur/gimeracil/oteracil as induction chemotherapy regimen for hypopharyngeal cancer

**Authors:** Cailing Jiang, Yulan Liu, Yunyan Mo, Lieyin Xu, Lin Zhu, Zhenya Li, Shengyuan Xu, Xi Qin, Guangteng Wu, Mafei Kang, Xiaosong He, Feng Xue

PMC · DOI: 10.3389/fonc.2025.1504658 · Frontiers in Oncology · 2025-02-24

## TL;DR

This study evaluates a new chemotherapy regimen for hypopharyngeal cancer, showing high response rates and manageable side effects.

## Contribution

The study introduces a novel combination of drugs for induction chemotherapy in hypopharyngeal cancer.

## Key findings

- The regimen achieved an 89.47% objective response rate and 100% disease control rate.
- A 71.43% pathological complete response rate was observed in patients who underwent surgery.
- Median progression-free survival was 17.6 months with no severe adverse events.

## Abstract

Treatment of hypopharyngeal carcinoma involves surgery, radiotherapy, and chemotherapy. The combination of docetaxel, cisplatin, and 5-fluorouracil as a standard induction chemotherapy regimen allows enhanced laryngeal preservation after surgery. In this study, our objective was to retrospectively analyze the short-term efficacy and adverse events of nab-paclitaxel plus cisplatin or nedaplatin plus tegafur/gimeracil/oteracil as an induction chemotherapy regimen for hypopharyngeal cancer.

This retrospective study involved 19 patients who received nab-paclitaxel plus cisplatin/nedaplatin plus tegafur/gimeracil/oteracil every 21 days intervals for three cycles at the Affiliated Hospital of Guilin Medical University (December 2020 to February 2023). The primary endpoint was progression-free survival. Adverse events were assessed in all patients.

Treatment response was evaluated after the second cycle. Clinical outcomes indicated that 2 (10.53%), 15 (78.94%), and 2 (10.53%) patients exhibited clinical complete response, partial response, and stable disease, respectively. The objective response and disease control rates were 89.47% (17/19) and 100%, respectively. The pathological complete response rate was 71.43% (5/7) among the seven patients who underwent surgery after three cycles. Following induction chemotherapy, 4 (21.05%), 2 (10.53%), and 2 (10.53%) patients received radiotherapy, chemotherapy, and chemotherapy plus immunotherapy, respectively, whereas 4 (21.05%) patients discontinued treatment. At the 17.43-month median follow-up, median progression-free survival was 17.6 months (95% confidence interval, 13.9-21.2). The most common grade 3 treatment-related adverse events were alopecia (36.8%), leukopenia (26.3%), and anemia (15.8%). No grade 4/5 treatment-emergent adverse events were observed.

The combination of nab-paclitaxel, cisplatin/nedaplatin, and tegafur/gimeracil/oteracil is a safe induction chemotherapy for treating hypopharyngeal cancer.

## Linked entities

- **Chemicals:** nab-paclitaxel (PubChem CID 36314), cisplatin (PubChem CID 5460033), nedaplatin (PubChem CID 9796440), tegafur (PubChem CID 5386), gimeracil (PubChem CID 54679224), oteracil (PubChem CID 4604)
- **Diseases:** hypopharyngeal cancer (MONDO:0005216)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** hypopharyngeal cancer (MESH:D007012), anemia (MESH:D000740), leukopenia (MESH:D007970), alopecia (MESH:D000505)
- **Chemicals:** gimeracil (MESH:C104201), cisplatin (MESH:D002945), paclitaxel (MESH:D017239), nedaplatin (MESH:C053989), 5-fluorouracil (MESH:D005472), tegafur (MESH:D005641), oteracil (MESH:D010094), docetaxel (MESH:D000077143)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11891220/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC11891220/full.md

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Source: https://tomesphere.com/paper/PMC11891220