Endostatin Adenovirus With Checkpoint Inhibitor in Advanced Head and Neck or Esophageal Cancer

Not Applicable

Not yet recruiting

• Conditions: Esophageal Cancer; Head and Neck Cancer (H&Amp;Amp;Amp;N)
• Interventions: Biological: recombinant human endostatin adenovirus; Drug: PD-1 Inhibitor

• Registration Number: NCT07154108
• Lead Sponsor: Sichuan University

Brief Summary

This is a Phase I, open-label, dual-cohort clinical trial designed to evaluate the safety, tolerability, and preliminary efficacy of intratumoral injection of recombinant human endostatin adenovirus in combination with a PD-1 inhibitor in patients with recurrent or metastatic head and neck cancer, or in patients with esophageal squamous cell carcinoma (ESCC) with superficial lymph node metastasis.

Detailed Description

Cohort A will enroll patients with recurrent or metastatic head and neck cancer. Cohort B will enroll patients with ESCC with superficial lymph node metastasis. Both cohorts will receive intratumoral injection of recombinant human endostatin adenovirus combined with intravenous an immune checkpoint inhibitor.

The primary objectives are to assess the safety profile, incidence of dose-limiting toxicities (DLTs), and treatment-related adverse events (TRAEs) of the combination therapy. The secondary objectives include evaluation of objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS). Each cohort plans to enroll approximately 20 patients, with a total of 40 participants.

Study Timeline

• Status Verified: 2025-08
• Study First Submitted: 2025-08-27
• Study First Submitted QC: 2025-08-27
• Last Update Submitted: 2025-08-27
• Study Start: 2025-09-01
• Study First Posted: 2025-09-04
• Last Update Posted: 2025-09-04
• Primary Completion: 2027-08-01
• Study Completion: 2027-08-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Age ≥18 years

   • Cohort A (Head and Neck Cancer): ≤70 years
   • Cohort B (Esophageal Squamous Cell Carcinoma): ≤75 years

2. Histologically or cytologically confirmed recurrent or metastatic:

   • Cohort A: Head and Neck Cancer
   • Cohort B: ESCC, AJCC 9th edition stage IV

3. Prior treatment:

   • Cohort A: ≥1 prior platinum-based chemotherapy regimen or platinum-refractory/intolerant
   • Cohort B: Prior immune checkpoint inhibitor (ICI) therapy with documented acquired resistance after prior PR or SD

4. At least one lesion accessible for intratumoral injection

   • Cohort A: measurable lesion ≥2 cm by RECIST 1.1
   • Cohort B: superficial metastatic lymph nodes (cervical or supraclavicular)

5. ECOG performance status

   • Cohort A: 0-2
   • Cohort B: 0-1

6. Adequate organ function

7. Life expectancy ≥12 weeks (Cohort A)

8. No anti-tumor therapy (chemotherapy, radiotherapy, biotherapy, antiviral) within 4 weeks prior to enrollment (Cohort A)

9. Availability of fresh tumor tissue specimen or pathological slides from the injection target lesion (Cohort B)

10. Male/female patients of childbearing potential must use effective contraception during study and for at least 6 months after treatment

11. Voluntary participation with signed informed consent

Exclusion Criteria

1. Known allergy or hypersensitivity to study drugs
2. Lesions unsuitable for injection due to proximity to major blood vessels, nerves, or hollow organs, or with extensive necrosis
3. Deeply located lesions with high procedural difficulty (Cohort B)
4. Concurrent radiotherapy to target lesion(s) (Cohort A)
5. Prior anti-angiogenic therapy (Cohort A)
6. Immunosuppressive therapy or systemic corticosteroids >10 mg/day prednisone (or equivalent) within 2 weeks prior to enrollment
7. Active autoimmune disease or history of autoimmune disease
8. Congenital or acquired immunodeficiency
9. Severe coagulopathy, bleeding tendency, or high-risk lesions (Cohort B)
10. Poor nutritional status (Cohort B)
11. Interstitial lung disease with symptoms or radiographic evidence (Cohort B)
12. Severe uncontrolled systemic disease or recent myocardial infarction (<3 months)
13. Acute infection
14. Pregnancy or breastfeeding
15. Other malignancy besides ESCC (Cohort B)
16. Patients unlikely to comply with follow-up or participation requirements
17. Any condition deemed unsuitable for enrollment by the investigator

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Endostatin Adenovirus+PD-1 inhibitor	recombinant human endostatin adenovirus	Recombinant Human Endostatin Adenovirus: Administered via intratumoral injection twice every 3 weeks for a total of eight doses, or until disease progression, the occurrence of unacceptable toxicity, or death from any cause, whichever occurs first. Immune checkpoint inhibitor: Administered via intravenous infusion once every 3 weeks. (This study includes two parallel cohorts: Cohort A (recurrent/metastatic head and neck cancer) and Cohort B (esophageal squamous cell carcinoma). Both cohorts will receive the same intervention.)
Endostatin Adenovirus+PD-1 inhibitor	PD-1 Inhibitor	Recombinant Human Endostatin Adenovirus: Administered via intratumoral injection twice every 3 weeks for a total of eight doses, or until disease progression, the occurrence of unacceptable toxicity, or death from any cause, whichever occurs first. Immune checkpoint inhibitor: Administered via intravenous infusion once every 3 weeks. (This study includes two parallel cohorts: Cohort A (recurrent/metastatic head and neck cancer) and Cohort B (esophageal squamous cell carcinoma). Both cohorts will receive the same intervention.)

Primary Outcome Measures

Name	Time	Method
Incidence of treatment-related adverse effects (TRAEs)	Through study completion, an average of 1.5 year	This study will collected any adverse medical events that occurred during the study drug treatment, and the treatment related adverse events as assessed by CTCAE v5.0.
Incidence of Dose-Limiting Toxicities (DLTs)	During the first cycle of treatment （21 days）	DLTs are defined as treatment-related adverse events occurring during the DLT evaluation period that meet protocol-specified criteria for severity and duration, as assessed by NCI CTCAE v5.0.

Secondary Outcome Measures

Name	Time	Method
Objective Response Rate (ORR)	up to 12 months	It is defined as the proportion of patients with complete response (CR) or partial response (PR), as assessed by RECIST 1.1.
Disease Control Rate (DCR)	up to 12 months	DCR refers to the proportion of patients who achieve complete response (CR), partial response (PR), or stable disease (SD) for a specified minimum duration after treatment, based on RECIST 1.1.
Progression-Free Survival (PFS)	up to 12 months	Time from the start of treatment to the first documentation of disease progression based on RECIST 1.1.
Overall Survival (OS)	up to 24 months	Time from the start of treatment to death from any cause

Trial Locations

Locations (1)

West China Hospital of Sichuan University; 🇨🇳 Chengdu, Sichuan, China