Chemotherapy, Radiation Therapy
Conditions
Keywords
Immumotherapy plus Chemotherapy, conversion therapy, advanced esophageal squamous cell carcinoma, chemoradiotherapy
Brief summary
The investigators conducted a phase II, prospective, two-arm clinical study to explore the efficacy of Camrelizumab combined with chemotherapy versus chemoradiotherapy for conversion therapy of potentially resectable advanced esophageal squamous cell carcinoma. This study will provide more evidence for conversion treatment of initially unresectable locally advanced esophageal squamous cell carcinoma and contribute to the development of treatment guidelines for esophageal cancer.
Detailed description
Esophageal cancer (EC) has a higher morbidity and mortality rate than most human malignancies. The standard treatment for unresectable locally advanced esophageal squamous cell carcinoma (ESCC) is concurrent chemoradiotherapy, but survival remains limited. Carrilizumab combined with chemotherapy has been shown to have an excellent pathological remission rate in the treatment of advanced esophageal cancer and locally advanced esophageal cancer. Here, the investigators conducted a phase II, prospective, two-arm clinical study to explore the efficacy of Camrelizumab combined with chemotherapy versus chemoradiotherapy for conversion therapy in potentially resectable advanced esophageal squamous cell carcinoma. All participants meeting the inclusion criteria will be registered after signing the informed consent form. Patients with thoracic esophageal cancer with clinical staging of T4a and T4b or at least one group of lymph nodes likely to invade surrounding organs or with concomitant enlarged lymph nodes unresectable will be included in the study. According to the study plan, patients who completed two cycles of chemotherapy combined with Camrelizumab induction or concurrent chemoradiotherapy were randomly assigned to receive radical surgery after being assessed as operable. The primary endpoint was R0 removal rate in patients undergoing surgery after treatment. Secondary endpoints were major pathological response (MPR) rate, overall survival (OS), progression-free survival (PFS), and adverse events. This study will provide more evidence for the conversion treatment of initially unresectable locally advanced esophageal squamous cell carcinoma and contribute to the development of treatment guidelines for esophageal cancer.
Interventions
DRUGCamrelizumab
200mgQ3w
DRUGPaclitaxel
175mg/m2，D1，Q3w
DRUGCisplatin
75mg/m2，D1，Q3w
RADIATIONRadiotherapy
41.4Gy, 1.8Gy each time, 5 times a week
Sponsors
Fujian Medical University Union Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* histologically-confirmed squamous cell carcinoma * primary lesions located in the thoracic esophagus * clinical stage cT4 or at least one group of lymph nodes invade the surrounding organs and unresectable lymph nodes * having not received neoadjuvant therapy * 18-75 years * ECOG performance status of 0 or 1 * no prior chemotherapy, radiotherapy, or immunotherapy for any cancers * adequate organ function * expectation of R0 resection * provision of written informed consent.
Exclusion criteria
* corticosteroid treatment (equivalent to prednisone \>10 mg/day) within 14 days before the first day of the drug administration * acquired immunodeficiency syndrome or active hepatitis B (DNA ≥ 104 copies/ml) or C (RNA ≥ 103 copies/ml) viral infections * history of pneumonitis or interstitial lung disease with clinical evidence, such as interstitial pneumonia and pulmonary fibrosis features on baseline CT scans * known or concurrent bleeding disorders or other uncontrolled diseases contraindicating surgical treatment * physical examination or clinical trial findings that can interfere with the results or put the patient at increased risk for treatment complications * comorbidities, including chronic pulmonary disease, poorly controlled hypertension, unstable angina, myocardial infarction within 6 months, and unstable mental disorders requiring therapy * allergy to drugs used in the study * participation in other clinical trials within 30 days before enrollment * ineligibility for participation based on the decision of investigators.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| R0 removal rate | up to 3 months | R0 removal rate in patients undergoing surgery after treatment |
| MPR rate | up to 4 months | major pathological response rate |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| OS | 12 months | overall survival |
| PFS | 12 months | progression-free survival |
Countries
China
Contacts
Primary ContactChun Chen, Prof
Outcome results
None listed