Overview
Adjuvant Therapy Versus Endoscopic Surgery Alone in Early-stage Recurrent Nasopharyngeal Carcinoma: A Multicenter Randomized Controlled Trial
Description
This study is an open-label, multicentered, evaluator-blinded , randomized clinical trial.
Patients with early-stage recurrent nasopharyngeal carcinoma were randomized into the control group and the experimental group. Patients in the control group would go through observation and follow-up after recurrent endoscopic surgery, while patients in the experimental group would be treated with adjuvant therapy such as chemotherapy and immunotherapy. A total of 176 subjects are required, with 88 patients in the control group and 88 patients in the experimental group.
Eligibility
Inclusion Criteria:
- Pathologically diagnosed with recurrent nasopharyngeal carcinoma;
- Stage rT1 or rT2(superficial parapharyngeal space, distance to internal carotid artery >5mm)or rT3 (confined to the bottom wall of the sphenoid sinus),according to AJCC 8th edition;
- Cervical lymph node metastasis can be controlled locally
- Age 18 to 75 years;
- Without distant metastasis;
- Informed consent forms signed;
- ≥6months from the accomplishment of radiation to recurrence
- previously radiotherapy for only 1 course;
- ECOG score 0-2 and can tolerate chemotherapy and immunotherapy
- Sufficient organ function;
- Undergone endoscopic surgery with negative pathological margin;
Exclusion Criteria:
- Participation in other interventional clinical trials;
- Uncontrolled illnesses which will interfere with the ability to undergo therapy;
- Suffering from another or multiple malignancy within 5 years (excluding fully treated basal cell or skin squamous cell carcinoma, cervical carcinoma in situ);
- Any contradiction to immune and chemotherapy;
- With serious autoimmune disease;
- Currently usage of immunosuppressive agents or systemic glucocorticoid therapy (dosage>10mg/day prednisone or other glucocorticoids), and continuing to use them within 2 weeks before the first administration of trial drugs;
- Severe allergic reactions to other monoclonal antibodies;
- History of radioactive particle planting;
- Vaccination with live vaccine within 4 weeks prior to initial administration or possibly during the study period;
- Female patients who are at pregnancy or lactation;
- Other situations that the researchers believe are not suitable for enrollment