Last updated: March 10, 2024
Sponsor: Sun Yat-sen University
Overall Status: Active - Recruiting
Phase
2
Condition
Carcinoma
Lung Cancer
Esophageal Cancer
Treatment
S-1
Toripalimab
Intensity-modulated radiotherapy
Clinical Study ID
NCT06187597
B2023-503
Ages 70-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Histologically confirmed squamous cell carcinoma of the esophagus;
- Locally advanced, and absence of hematogenous metastasis disease according to UICC TNMversion 8;
- Not suitable for surgery (either for medical reasons or patient's choice);
- Age at diagnosis 70 to 85 years;
- No prior cancer therapy;
- Estimated life expectancy >6 months;
- Eastern Cooperative Oncology Group performance status ≤ 2
- No history of concomitant or previous malignancy;
- The function of important organs meets the following requirements: a. white blood cellcount (WBC) ≥4.0×109/L, absolute neutrophil count (ANC) ≥1.5×109/L; b. platelets ≥100×109/L; c. hemoglobin ≥9g/dL; d. serum albumin ≥2.8g/dL; e. total bilirubin ≤1.5×ULN, ALT, AST and/or AKP ≤2.5×ULN; f. serum creatinine ≤1.5×ULN or creatinineclearance rate >60 mL/min;
- Ability to understand the study and sign informed consent.
Exclusion
Exclusion Criteria:
- Patients who have been treated previously with anti-tumor therapy (includingchemotherapy, radiotherapy, surgery, immunotherapy, etc.);
- Patients with hematogenous metastasis disease or esophageal fistula at diagnosis;
- Known or suspected allergy or hypersensitivity to monoclonal antibodies, anyingredients of cadonilimab, and the chemotherapeutic drugs paclitaxel or cisplatin;
- Patients who have a preexisting or coexisting bleeding disorder;
- Inability to provide informed consent due to psychological, familial, social and otherfactors;
- Presence of CTC grade ≥2 peripheral neuropathy;
- A history of malignancies other than esophageal cancer before enrollment, excludingnon-melanoma skin cancer, in situ cervical cancer, or cured early prostate cancer
- A history of diabetes for more than 10 years and poorly controlled blood glucoselevels;
- Patients who cannot tolerate chemoradiotherapy due to severe cardiac, lung, liver orkidney dysfunction, or hematopoietic disease or cachexia.
- Active autoimmune diseases, a history of autoimmune diseases (including but notlimited to these diseases or syndromes, such as colitis, hepatitis, hyperthyroidism),a history of immunodeficiency (including a positive HIV test result), or otheracquired or congenital immunodeficiency diseases, a history of organ transplantationor allogeneic bone marrow transplantation;
- A history of interstitial lung disease or non-infectious pneumonia;
- A history of active pulmonary tuberculosis infection within 1 year or a history ofactive pulmonary tuberculosis infection more than 1 year ago but without formalanti-tuberculosis treatment;
- Presence of active hepatitis B (HBV DNA ≥ 2000 IU/mL or 104 copies/mL), hepatitis C (positive for hepatitis C antibody, and HCV-RNA levels higher than the lower limit ofthe assay).
Study Design
Total Participants: 140
Treatment Group(s): 3
Primary Treatment: S-1
Phase: 2
Study Start date:
March 01, 2024
Estimated Completion Date:
December 31, 2028
Study Description
Connect with a study center
Mian Xi
Guangzhou, Guangdong 510060
ChinaActive - Recruiting

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