NCT07339488 Intestinal Low-Dose Radiotherapy Plus Immunochemotherapy for Conversion of Borderline Resectable/Unresectable Esophageal Squamous Cell Carcinoma

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 43 participants in total. It began in 2025-12-05 with a primary completion date of 2028-11-01.

Brief Summary

Esophageal cancer (EC) ranks among the leading malignant gastrointestinal tumors globally in terms of both incidence and mortality. Cases of EC in China account for over 50% of the global total, with squamous cell carcinoma being the primary pathological type. Locally advanced EC (LAEC), particularly cases where radical surgical resection is not feasible, exhibits high recurrence rates and low 5-year survival rates. However, studies have shown that patients with LAEC who undergo comprehensive treatment followed by surgery experience significantly prolonged survival and improved quality of life compared to those who do not receive surgical intervention. Current conversion treatment regimens under investigation include: chemotherapy alone, chemoradiotherapy, immunotherapy combined with chemotherapy, and immunotherapy combined with chemoradiotherapy-each of these approaches has distinct advantages and limitations. Immunochemotherapy has emerged as a current research focus: it not only demonstrates significantly superior efficacy compared to chemotherapy alone but also exhibits lower cumulative toxicity than radiotherapy-combined conversion regimens, resulting in a more favorable overall benefit-risk ratio. As such, it represents the most promising conversion treatment strategy. Retrospective and prospective clinical studies have shown that low-dose radiotherapy targeting the small intestine can enhance the anti-tumor response of immune checkpoint inhibitors (ICIs) in patients with advanced solid tumor, prolong their overall survival, and increase the incidence of the abscopal effect. Further mechanistic investigations have revealed that intestinal low-dose radiotherapy (ILDR) may augment the immune cancerous lethality by modulating the gut microbiota and their metabolic profiles. Based on the findings from these preliminary studies, the current research plans to conduct a prospective phase II single-arm clinical trial to investigate the efficacy and safety of ILDR combined with immunochemotherapy as conversion therapy in patients with borderline resectable or unresectable esophageal squamous cell carcinoma (BR/UR ESCC). This research plans to enroll at least 39 evaluable cases or a total of 43 cases in two seperated stages, focusing on patients with thoracic BR/UR ESCC. Patients will receive a single fraction of ILDR with a mean dose of 1 Gy, concurrently with 3 cycles of albumin-bound paclitaxel (260 mg/m² on day 1), cisplatin (75 mg/m² on day 1), and tislelizumab (200 mg on day 1). The efficacy and safety of the treatment will be evaluated throughout the study.

Eligibility Criteria

Inclusion Criteria: 1. Patients voluntarily enroll in this study, sign an informed consent form, and demonstrate good compliance. 2. Age ≥18 years and ≤75 years; both sexes are eligible. 3. ECOG performance status score of 0-1. 4. Pathologically confirmed esophageal squamous cell carcinoma (ESCC) prior to surgery. 5. Thoracic esophageal cancer. 6. Unresectable lesions, defined as: T4 stage; marginally resectable T3 stage (invading other organs, e.g., trachea, bronchus, or aorta not ruled out by imaging); presence or absence of unresectable lymph nodes or metastatic lymph nodes invading adjacent organs; presence or absence of supraclavicular lymph node metastasis; or clinically confirmed unresectable disease by the surgeon. 7. No prior history of anti-tumor treatment, including chemotherapy, hormonal therapy, radiotherapy, or immunotherapy. 8. Baseline laboratory requirements (within 7 days prior to enrollment): Hematology: 1. Hb≥90 g/L (no transfusion within 14 days) 2. NEUT ≥1.5×10⁹/L 3. PLT ≥100×10⁹/L 4. WBC≥3×10⁹/L Biochemistry: 1. ALT and AST≤2.5×ULN 2. TBIL≤1.5×ULN 3. SCr≤1.5×ULN; or CrCl≥60 mL/min Coagulation: APTT, INR, and PT≤1.5×ULN Thyroid function: TSH≤ULN (if abnormal, FT3/FT4 levels should also be considered; eligible if FT3/FT4 are normal) Echocardiography: LVEF≥50% 9. Female subjects need to agree to use contraception during the study and for 6 months post-study; serum pregnancy test negative within 7 days prior to enrollment; non-lactating. Male subjects must agree to use contraception during the study and for 6 months post-study. 10. No psychological, familial, social, or geographical factors that may impair protocol adherence. 11. Other parameters meet general clinical trial enrollment criteria. 12. The subject or authorized representative has read, fully understands the patient information sheet, and signed the informed consent form. Exclusion Criteria: 1. Patients with distant metastases other than supraclavicular lymph node metastases. 2. Presence or high risk of esophageal perforation. 3. Patients with contraindications to radiotherapy or immune checkpoint inhibitor (ICI) therapy. 4. Patients who previously experienced unacceptable toxicity after receiving ICI therapy. 5. Patients with a history of thoracoabdominal/pelvic radiotherapy within 6 months prior to enrollment. 6. Adverse reactions from prior anti-tumor treatment have not recovered to CTCAE v5.0 grade≤1 (excluding toxicities deemed by the investigator to pose no safety risk, such as fatigue or alopecia). 7. Subjects with active, uncontrolled systemic bacterial, viral, or fungal infections despite optimal treatment. 8. Respiratory depression, airway obstruction, or tissue hypoxia. 9. Severe cardiac disease (i.e., NYHA functional class II or higher). 10. Markedly abnormal liver or kidney function (i.e., indicators \>3 times the upper limit of normal). 11. Active hepatitis B, hepatitis C, HIV, or syphilis. 12. Active brain disease or central nervous system/meningeal metastases with significant symptoms, or impaired decision-making capacity. 13. Hypersensitivity to drugs included in the trial. 14. Drug and/or alcohol abuse. 15. Pregnant or lactating women. 16. Concurrent participation in another therapeutic clinical trial. 17. Major surgical procedure within 30 days prior to enrollment. 18. Use of antibiotics, antifungals, antivirals, or antiparasitics within 4 weeks prior to registration.

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