Skip to content

Efficacy and Safety of Anlotinib combined with Penpulimab in Patients with Resectable Locally Advanced Esophageal Squamous Cell Carcinoma

Efficacy and Safety of Anlotinib combined with Penpulimab in Patients with Resectable Locally Advanced Esophageal Squamous Cell Carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064848
Enrollment
Unknown
Registered
2022-10-20
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal cancer

Interventions

Experimental group:Anlotinib combined with Penpulimab

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. No gender limit, patients aged 18-75 years; 2. Primary esophageal squamous cell carcinoma confirmed by pathology (including histology or cytology); 3. Patients with clinical stage of cT1b-cT2N +M0 or cT2-cT4a, any N, M0, who have been judged feasible for radical resection of esophageal cancer and need neoadjuvant therapy before surgery; 4. Patients are not eligible for neoadjuvant chemoradiotherapy due to their physical conditions, mainly including: (1) Patients aged >=70 years who are not recommended for concurrent chemoradiotherapy; (2) PS > 1 score; (3) Patients with lung underlying diseases and other reasons not eligible for concurrent chemoradiotherapy; 5. ECOG (Eastern Oncology Consortium) score: 0-2; 6. Normal function of major organs.

Exclusion criteria

Exclusion criteria: 1. Previously received surgery, radiotherapy, chemotherapy, targeted or immunotherapy for esophageal squamous cell carcinoma; 2. Patients with distant organ metastasis; 3. Patients with esophageal squamous cell carcinoma with active bleeding within 2 months of the primary lesion; Patients with tumor invasion of bronchus or large blood vessels and bleeding tendency; 4. Accompanied by other immune diseases, or long-term use of immunosuppressive agents or hormones; 5. Complicated with tumors of other organs; 6. Patients are difficult to communicate, or difficult to follow up for a long time; 7. The doctor feels that other circumstances are not appropriate.

Design outcomes

Primary

MeasureTime frame
Pathologic complete response rate;

Secondary

MeasureTime frame
Objective response rate;1-year disease-free survival rates;

Countries

China

Contacts

Public ContactDing Zhenyu

West China Hospital, Sichuan University

dingzhenyu@scu.edu.cn+86 18980601957

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026