RecruitingPhase 3NCT04138212

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

Neoadjuvant Chemotherapy Versus Neoadjuvant Chemoradiotherapy for Resectable Locally Advanced Esophageal Squamous Cell Carcinoma: a Randomized, Controlled Clinical Trial (HCHTOG1903)


Sponsor

Henan Cancer Hospital

Enrollment

456 participants

Start Date

Oct 22, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two approaches to treating locally advanced cancer of the esophagus (the tube connecting the mouth to the stomach) before surgery: chemotherapy alone versus chemotherapy combined with radiation therapy. **You may be eligible if...** - You have confirmed squamous cell carcinoma of the thoracic esophagus at stage T2-T4a, N+ or T3-4a N0 (locally advanced but not spread to distant areas) - Your lymph node involvement is confined to the area (no spread to the neck lymph nodes) - You have not received any prior anti-cancer treatment - You are medically fit for both surgery and chemotherapy or chemoradiation - Your performance status (PS score) is 0 or 1 **You may NOT be eligible if...** - You have had prior cancer treatment - You have another active cancer - Your tumor is very large (8 cm or longer, or 5 cm or wider) - You require ongoing steroid treatment - You had a heart attack in the past 6 months - You have a psychotic disorder - You are pregnant Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPaclitaxel, Cisplatin

Paclitaxel 175mg/m2 plus Cisplatin 75mg/m2, q21d, 2 cycles

RADIATIONneoadjuvant chemoradiation therapy

Paclitaxel 50mg/m2 plus Carboplatin AUC=2, q1w, 5 cycles; 41.4Gy, 1.8Gy/d\*23


Locations(1)

Henan Cancer Hospital

Zhengzhou, Henan, China

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NCT04138212


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