Evidence map›Paper›PMID 42718586›Full record

ArticleFrontiers in oncology2026

Efficacy and safety of neoadjuvant treatment with PD-1 inhibitor in locally advanced head and neck squamous cell carcinoma.

Shaowei Xu, Hongxin Zheng, Xiaoqi Liao, Manyu Jiang, Hanwei Peng, Muyuan Liu

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Shaowei Xu *Department of Head, Neck and Thyroid Surgery, Cancer Hospital of Shantou University Medical College, Shantou, China.
Hongxin Zheng *Department of Head, Neck and Thyroid Surgery, Cancer Hospital of Shantou University Medical College, Shantou, China.
Xiaoqi LiaoDepartment of Department of Otorhinolaryngology, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Manyu JiangDepartment of General Surgery, Puning People's Hospital, Puning, China.
Hanwei PengDepartment of Head, Neck and Thyroid Surgery, Cancer Hospital of Shantou University Medical College, Shantou, China.
Muyuan LiuDepartment of Head, Neck and Thyroid Surgery, Cancer Hospital of Shantou University Medical College, Shantou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a common malignant tumor. Traditional treatments have unstable efficacy, with risks of relapse, drug resistance and side effects. Immunotherapy has achieved good results in recurrent/metastatic advanced HNSCC, but relevant research on its neoadjuvant application is insufficient. This study retrospectively analyzes clinical data to evaluate the efficacy and safety of PD-1 inhibitors as neoadjuvant therapy for LA-HNSCC, providing a scientific basis for treatment strategies. This study conducted a retrospective analysis of patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) treated at Shantou University Cancer Hospital from November 2020 to March 2024. The experimental group was administered neoadjuvant PD-1 inhibitor combined with chemotherapy, while the control group received chemotherapy alone. Efficacy was evaluated in accordance with RECIST 1.1 criteria, and treatment-related adverse events were graded based on CTCAE 5.0. SPSS 27.0 software and Kaplan-Meier method were employed for statistical analysis, with p<0.05 considered statistically significant. Baseline characteristics were well balanced between the two groups (P>0.05), with no significant difference in RECIST-based efficacy outcomes (P>0.05). The study group exhibited a significantly higher pathological downgrading rate and pathological complete response (pCR) (P = 0.032), a favorable safety profile, and improved overall survival (OS) (P = 0.044). Neoadjuvant immunochemotherapy was associated with improved overall survival, and surgery was associated with a lower risk of death. These findings are exploratory and require confirmation in larger prospective studies. Neoadjuvant immunochemotherapy was associated with improved pathological response and OS in LA-HNSCC, with an acceptable safety profile. These exploratory findings warrant confirmation in larger prospective studies.a retrospective analysis of patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) treated at Shantou University Cancer Hospital from November 2020 to March 2024. The experimental group was administered neoadjuvant PD-1 inhibitor combined with chemotherapy, while the control group received chemotherapy alone. Efficacy was evaluated in accordance with RECIST 1.1 criteria, and treatment-related adverse events were graded based on CTCAE 5.0. SPSS 27.0 software and Kaplan-Meier method were employed for statistical analysis, with p<0.05 considered statistically significant. Baseline characteristics were well balanced between the two groups (P>0.05), with no significant difference in RECIST-based efficacy outcomes (P>0.05). The study group exhibited a significantly higher pathological downgrading rate and pathological complete response (pCR) (P = 0.032), a favorable safety profile, and improved overall survival (OS) (P = 0.044). Neoadjuvant treatment regimen and surgical intervention were identified as factors associated with improved OS. These should be interpreted as exploratory given the sample size and group imbalance. Neoadjuvant immunochemotherapy was associated with improved pathological response and OS in LA-HNSCC, with an acceptable safety profile. These exploratory findings warrant confirmation in larger prospective studies. A retrospective analysis of patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) treated at Shantou University Cancer Hospital from November 2020 to March 2024. The experimental group was administered neoadjuvant PD-1 inhibitor combined with chemotherapy, while the control group received chemotherapy alone. Efficacy was evaluated in accordance with RECIST 1.1 criteria, and treatment-related adverse events were graded based on CTCAE 5.0. SPSS 27.0 software and Kaplan-Meier method were employed for statistical analysis, with p<0.05 considered statistically significant. Baseline characteristics were well balanced between the two groups (P>0.05), with no significant difference in RECIST-based efficacy outcomes (P>0.05). The study group exhibited a significantly higher pathological downgrading rate and pathological complete response (pCR) (P = 0.032), a favorable safety profile, and improved overall survival (OS) (P = 0.044). Neoadjuvant treatment regimen and surgical intervention were identified as factors associated with improved OS. These should be interpreted as exploratory given the sample size and group imbalance. Neoadjuvant immunochemotherapy was associated with improved pathological response and OS in LA-HNSCC, with an acceptable safety profile. These exploratory findings warrant confirmation in larger prospective studies. A retrospective analysis of patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) treated at Shantou University Cancer Hospital from November 2020 to March 2024. The experimental group was administered neoadjuvant PD-1 inhibitor combined with chemotherapy, while the control group received chemotherapy alone. Efficacy was evaluated in accordance with RECIST 1.1 criteria, and treatment-related adverse events were graded based on CTCAE 5.0. SPSS 27.0 software and Kaplan-Meier method were employed for statistical analysis, with p<0.05 considered statistically significant. Baseline characteristics were well balanced between the two groups (P>0.05), with no significant difference in RECIST-based efficacy outcomes (P>0.05). The study group exhibited a significantly higher pathological downgrading rate and pathological complete response (pCR) (P = 0.032), a favorable safety profile, and improved overall survival (OS) (P = 0.044). Neoadjuvant immunochemotherapy was associated with improved overall survival, and surgery was associated with a lower risk of death. These findings are exploratory and require confirmation in larger prospective studies. Neoadjuvant immunochemotherapy was associated with improved pathological response and OS in LA-HNSCC, with an acceptable safety profile. These exploratory findings warrant confirmation in larger prospective studies.

Indexed as

head and neck squamous cell carcinoma (HNSC)immunotherapyneoadjuvant therapy (NACT)PD-1inhibitorsPD-L1 inhibitors

Identifiers

PMID42718586
PMCPMC13553248

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.