Overview

Neoadjuvant Chemoradiotherapy Combined With Perioperative Toripalimab in Locally Advanced Esophageal Cancer

Status:
Recruiting
Trial end date:
2023-12-31
Target enrollment:
0
Participant gender:
All
Summary
Neoadjuvant chemoradiotherapy (CRT) followed by surgery has become the standard treatment option for locally advanced esophageal squamous cell cancer (ESCC). However, only 20% to 40% of patients can achieve pathologic complete response (pCR) after neoadjuvant CRT with favorable prognosis and about 10% of patients have disease progression after chemoradiotherapy. How to improve the the efficacy of neoadjuvant therapy is an important clinical problem to be solved. Immunotherapy targeting the PD-1/PD-L1 checkpoints has demonstrated promising activity in advanced EC especially in ESCC. In Keynote181 study, for patients with metastatic esophageal squamous cell carcinoma, regardless of PD-L1 expression, pembrolizumab significantly improved overall survival compared with chemotherapy. However, the efficacy and safety of immunotherapy therapy in surgery-based multidisciplinary treatment of local advanced esophageal cancer still need a lot of clinical studies to further confirm. The aim of this study was to evaluate the efficacy and safety of the neoadjuvant chemoradiotherapy combined with perioperative toripalimab in patients with locally advanced esophageal squamous cell cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
RenJi Hospital
Criteria
Inclusion Criteria:

- Aged 18 to 75 years old of either gender

- Patients with histopathological confirmed resectable thoracic esophageal squamous cell
carcinoma who are anti-tumor treatment-naive;

- Clinical stage of T1-4aN1-2M0 or T3-4aN0M0 according to the 8th edition of the UICC
staging system;

- ECOG PS score of 0-1;

- The indexes of hematology, biochemistry and organ function meet the following
requirements: a. white blood cell count (WBC) ≥ 3.0×109/L;b. neutrophil count (ANC) ≥
1.5×109/L; c. platelets ≥ 85×109/L; d. hemoglobin ≥ 9g/dL; e. total bilirubin ≤
14.4µmol/L; f. ALT ≤ 75U/L; g. serum creatinine ≤ 104µmol/L and creatinine clearance
rate >60 mL/min;

- Women of childbearing age must undergo a pregnancy test within 7 days before enrolling
in the treatment, and those who are negative can be enrolled. Patients of childbearing
age and their sexual partners agree to use reliable methods of contraception before
entering the study, during the study, and at least 180 days after the end of the
study;

- Ability to understand the study and sign informed consent.

Exclusion Criteria:

- Patients with active infection within 2 weeks before the first use of the study drug
or need to be treated with oral or intravenous antibiotics;

- A history of interstitial lung disease or non-infectious pneumonia;

- Patients whose clinician judges surgery as the first choice for the best treatment;

- A history of autoimmune diseases or abnormal immune system ;

- Patients who cannot tolerate chemoradiotherapy or surgery due to severe cardiac, lung
dysfunction。

- Patients diagnosed with any other malignant tumor within 5 years before enrollment,
except for malignant tumors with low risk of recurrence and risk of death, such as
fully treated basal cell or squamous cell skin and carcinoma in situ of the cervix;

- Known or suspected allergy or hypersensitivity to monoclonal antibodies, any
ingredients of Toripalimab, and the chemotherapeutic drugs paclitaxel or cisplatin;

- A history of immunodeficiency,including a positive HIV test result or other acquired
or congenital immunodeficiency diseases, a history of organ transplantation or
allogeneic bone marrow transplantation;

- Women during pregnancy or lactation;

- Other situations not suitable for enrollment.