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Study identifier: NCT05740995 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neoadjuvant Anti-PD-1 Plus Chemotherapy in Locally Advanced Resectable Esophageal Squamous Cell Carcinoma

Condition: Esophageal Squamous Cell Carcinoma · Neoadjuvant Chemoimmunotherapy  ·  Sponsor: Shanghai Zhongshan Hospital

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the outcomes and identify predictors of neoadjuvant anti-PD-1 plus chemotherapy in locally advanced resectable esophageal squamous cell carcinoma (ESCC). In this single-center cohort study, we are aiming to (1) evaluate the therapeutic efficacy and survival benefits on patients with locally advanced resectable ESCC (cT3-4aN0-1M0); (2) evaluate the value of genomic indicators including MMR alternation status in predicting therapeutic responses and prognosis; (3) evaluate the value of transcriptomic indicators including B cell lineage features in predicting therapeutic responses and prognosis; (4) evaluate the value of microbial and metabolite indicators in predicting therapeutic responses and prognosis. Whole exome sequencing, RNA sequencing, 16S rRNA sequencing and Liquid Chromatography with tandem mass spectrometry (LC-MS-MS) of samples of patients to neoadjuvant chemoimmunotherapy before and after treatment are performed to explore the mechanisms of drug resistance and identification of predictive and prognosis biomarkers.

This description comes directly from the study's public registry record.

Talk to the study team

Jie Gu, MD  ·  +86 13611972978  ·  gu.jie3@zs-hospital.sh.cn

Di Ge, MD  ·  ge.di@zs-hospital.sh.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Zhongshan Hospital, Fudan UniversityShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05740995