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Study identifier: NCT04138212 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Neoadjuvant Chemotherapy Versus Neoadjuvant Chemoradiotherapy for Resectable Locally Advanced Esophageal Cancer (HCHTOG1903)

Condition: Esophageal Squamous Cell Carcinoma  ·  Sponsor: Henan Cancer Hospital

PhasePhase 3
Planned participants456
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

Multimodal treatment combining surgery with chemotherapy and/or radiotherapy is necessary to improve the chances of survival in patients with locally advanced thoracic esophageal cancer. However, there is no consensus about the neoadjuvant treatment for resectable locally advanced esophageal squamous cell carcinoma. The aim of current randomized controlled clinical trail is to investigate the impact of neoadjuvant chemotherapy plus surgery and neoadjuvant chemoradiation therapy plus surgery on overall survival for patients with resectable locally advanced esophageal squamous cell carcinoma. The investigators plan to enroll 456 patients with locally advanced esophageal squamous cell carcinoma in 3 years. Eligible patients will be randomized into neoadjuvant chemotherapy group (paclitaxel 175mg/m2 plus cisplatin 75mg/m2, q21d, 2 cycles) or neoadjuvant chemoradiation group (41.4Gy, 1.8Gy\*23d plus paclitaxel 50mg/m2 plus carboplatin AUC=2, q1w, 5 cycles). The primary endpoint is 5 year overall survival and the secondary endpoints include 5 year disease-free survival, adverse events, pathologic complete response, postoperative complications, quality of life. The biomarkers predicting the sensitivity of neoadjuvant therapy will be explored.

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

Talk to the study team

Haibo Sun  ·  +8615188301091  ·  sunny-haipo@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Henan Cancer HospitalZhengzhou, Henan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04138212