A Study of Neoadjuvant Therapy for the Treatment of Patients With Locally Advanced Esophageal Squamous Cell Carcinoma

Phase 2

Recruiting

• Conditions: Neoadjuvant Therapy; Esophageal Squamous Cell Carcinoma
• Interventions: Radiation: Thoracic radiotherapy; Drug: anlotinib

• Registration Number: NCT06354530
• Lead Sponsor: Army Medical Center of PLA

Brief Summary

The goal of this interventional study is to compare the safety and efficacy of neoadjuvant immunotherapy plus chemotherapy and anlotinib versus immunotherapy combined with concurrent chemoradiotherapy in the treatment of locally advanced esophageal squamous cell carcinoma. The main question it aims to answer is: To evaluate the safety and efficacy of neoadjuvant immunotherapy plus chemotherapy and anlotinib versus immunotherapy combined with concurrent chemoradiotherapy in patients with locally advanced esophageal squamous cell carcinoma and to explore the optimal preoperative neoadjuvant treatment regimen for esophageal squamous cell carcinoma.

Detailed Description

The goal of this single-center, open-label, non-inferior, randomized controlled, interventional study is to compare the safety and efficacy of neoadjuvant immunotherapy plus chemotherapy and anlotinib versus immunotherapy combined with concurrent chemoradiotherapy in the treatment of locally advanced esophageal squamous cell carcinoma. The main question it aims to answer is: To evaluate the safety and efficacy of neoadjuvant immunotherapy plus chemotherapy and anlotinib versus immunotherapy combined with concurrent chemoradiotherapy in patients with locally advanced esophageal squamous cell carcinoma and to explore the optimal preoperative neoadjuvant treatment regimen for esophageal squamous cell carcinoma.

Study Timeline

• Study Start: 2024-03-08
• Study First Submitted: 2024-03-18
• Status Verified: 2024-04
• Study First Submitted QC: 2024-04-03
• Last Update Submitted: 2024-04-03
• Study First Posted: 2024-04-09
• Last Update Posted: 2024-04-09
• Primary Completion: 2025-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 266

Inclusion Criteria

• Surgically resectable cT1-4aN+M0 or cT3-4aN0M0 esophageal squamous cell carcinoma initially diagnosed by histology or cytology
• Patients who can take anlotinib capsules orally
• No previous systematic antitumor treatment
• ECOG PS 0-1
• The function of important organs meets the following requirements: absolute neutrophil count≥1.5×10^9 / L; platelet≥80×10^9 / L; hemoglobin≥80×10^9 / L; total bilirubin≤1.5×upper limit of normal; within normal serum creatinine; ALT and glutamatergic aminase≤2.5× upper limit of normal
• No incurable serious complications or other major diseases
• The thoracic surgeon judges that the operation can be tolerated
• Female subjects with fertility, and male subjects with childbearing partners, required a medically approved contraceptive during study treatment and at least 6 months after the last chemotherapy
• The subjects volunteered to join the study, signed informed consent, had good compliance and cooperated with follow-up

Exclusion Criteria

• BMI<18.5kg/m2 or 10% weight loss in 2 months before screening (while considering the effect of large chest ascites on body weight)
• Patients with tracheal / bronchial / macrovascular invasion, deep ulcer esophagus, digestive tract perforation and / or fistula, major bleeding, and poor lung function or previous chronic lung disease within 6 months prior to initial medication
• Patients with significant feeding obstruction unable to take oral anlotinib
• Known history of allergy to any component of biological or PD-1 mab formulation, albumin-bound paclitaxel, carboplatin and other platinum drugs manufactured by Chinese hamster ovary cells (CHO)
• Have received any of the following treatments: any investigational drug; enrolled in another clinical study except for an observational (non-interventional) clinical study; received anti-tumor or live vaccine
• A history of active autoimmune diseases and autoimmune diseases
• A history of immunodeficiency, including a positive HIV test, or other acquired, congenital immunodeficiency disorders, or a history of organ transplantation and allogeneic bone marrow transplantation
• The subject had cardiovascular clinical symptoms or disease that were not well controlled
• Patients with active hepatitis B or hepatitis C and active pulmonary tuberculosis
• Severe infection (CTCAE> 2) occurred within 4 weeks prior to initial use of study drug, such as severe pneumonia, bacteremia, infection requiring hospitalization; baseline chest imaging indicated active lung inflammation, symptoms and signs of infection within 2 weeks prior to initial use of study drug or the need for oral or intravenous antibiotics, except for prophylactic antibiotics
• Major surgery (except diagnostic surgery) within 28 days prior to treatment, or is expected to undergo major surgery during the study
• Any other malignancy had been diagnosed within 5 years prior to the first use of study drug, except for nausea tumors with low risk and mortality (5-year survival> 90%), such as adequately treated basal or squamous cell skin carcinoma or carcinoma of the cervix
• Female patients during pregnancy or lactation and who were refused or unable to use contraception
• At the discretion of the investigator, the subject had other factors that could contribute to his forced termination

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
neoadjuvant immunotherapy plus chemotherapy and anlotinib	Thoracic radiotherapy	neoadjuvant immunotherapy plus chemotherapy and anlotinib
neoadjuvant immunotherapy combined with concurrent chemoradiotherapy	anlotinib	neoadjuvant immunotherapy combined with concurrent chemoradiotherapy

Primary Outcome Measures

Name	Time	Method
Pathological complete response (pCR), Major pathological response (MPR)	Up to approximately 15 weeks after randomization	Defined as the lack of any viable tumour cells after complete evaluation in the resected lung cancer specimen and all sampled regional lymph nodes
Major pathological response (MPR)	Up to approximately 15 weeks after randomization	Major pathological response (MPR)

Secondary Outcome Measures

Name	Time	Method
3-year disease free survival	From date of randomization to approximately 3 years after date of resection	3-year disease free survival
Objective response rate (ORR)	Up to approximately 15 weeks after randomization	Objective response rate (ORR)
R0 excision rate	Up to approximately 15 weeks after randomization	R0 excision rate
3-year overall survival	From date of randomization to approximately 3 years after date of resection	3-year overall survival

Trial Locations

Locations (1)

Army Medical Center of PLA; 🇨🇳 Chongqing, None Selected, China