About this trial
This study is to investigate the efficacy and safety of the induction chemotherapy + concurrent chemoradiotherapy(CCRT)combined with toripalimab and endostar treatment, in comparison with the induction chemotherapy + concurrent chemoradiotherapy(CCRT), in treating locally advanced high-risk nasopharyngeal carcinoma
Eligibility criteria
Qualifiers
With ECOG score 0-1.
Subjective aged 18-65 years, male or non-pregnant female.
Pathologically diagnosed as nasopharyngeal non-keratinizing carcinoma (differentiated or undifferentiated, i.e., the WHO type II or III).
Stage IVa (8th AJCC/UICC stage) T4 and/or N3, untreated patients with nasopharyngeal carcinoma.
Disqualifiers
Patients with nasopharyngeal carcinoma with recurrence and distant metastasis.
Pathologically diagnosed as keratinizing squamous cell carcinoma (WHO classification type I).
Patients who had undergone radiotherapy or systemic chemotherapy.
Pregnant or breastfeeding females, or females in fertility period while with no effective contraceptive measures.
Trial design
Treatments tested in this trial
- Toripalimab, Endostar Combined With Radiotherapy and Chemotherapy
- IC+CCRT
Treatment groups
Locations
Sponsors and collaborators
First Affiliated Hospital of Guangxi Medical University
Lead sponsor
Shandong Cancer Hospital and Institute
Collaborator
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Collaborator
The Affiliated Hospital Of Guizhou Medical University
Collaborator
Xiangya Hospital of Central South University
Collaborator
Jiangxi Provincial Cancer Hospital
Collaborator
Zhejiang Cancer Hospital
Collaborator
Fourth Affiliated Hospital of Guangxi Medical University
Collaborator
LiuZhou People's Hospital
Collaborator
Guilin Medical College
Collaborator
Affiliated Hospital of North Sichuan Medical College
Collaborator