RecruitingNCT06009705

Toripalimab Combined With Radiotherapy and S-1 for Older Patients With Esophageal Cancer

Efficacy and Safety of Toripalimab Combined With Radiotherapy and S-1 Followed by Adjuvant Toripalimab Maintenance Therapy for Older Patients With Esophageal Cancer


Sponsor

Hebei Medical University Fourth Hospital

Enrollment

56 participants

Start Date

Oct 1, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

This trial aims to assess efficacy and safety of toripalimab combined with radiotherapy and S-1 followed by adjuvant toripalimab maintenance therapy for older patients with stage II-III esophageal cancer.


Eligibility

Min Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of immunotherapy (toripalimab), oral chemotherapy (S-1), and radiation therapy for older patients (65+) with esophageal cancer who cannot or choose not to have surgery. **You may be eligible if...** - You are 65 or older - You have confirmed esophageal cancer (stage I–III) - You are unable to have surgery or have chosen not to - You are well enough to tolerate immunotherapy combined with chemotherapy and radiation (ECOG 0–2) - Your blood counts, liver, kidney, heart, and lung function are within acceptable ranges - You have at least one measurable tumor - You have a life expectancy of at least 6 months **You may NOT be eligible if...** - Your cancer has spread to distant organs - You have serious heart, lung, liver, or kidney problems - You are pregnant or breastfeeding - You have a history of severe immune-related conditions 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

DRUGtoripalimab

JS001, the active ingredient of toripalimab injection, independently developed by Shanghai Junshi Biomedical Technology Co., Ltd, is an independently developed novel recombinant humanised (degree of 97%) anti-PD-1 monoclonal antibody (Chinese Patent License No. CN104250302B, PCT Patent Publication No. WO2014/206107A1), belonging to the human IgG4/Kappa subtype, and introducing a point mutation at the Serine to Proline (S228P) protein site 228 in the hinge region of the IgG4 heavy chain.


Locations(1)

Fourth Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

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NCT06009705


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