This study is a retrospective real-world study. In this study, we plan to collect the clinical data of LASCCHN patients who received chemoradiotherapy combined with or without nimotuzumab .
This study is a retrospective real-world study. The diagnosis and treatment of patients, disease management, and information collection are completely dependent on the daily medical practice. In this study, we plan to select 5 to 8 hospitals nationwide to collect the clinical data of LASCCHN patients who received chemoradiotherapy combined with or without nimotuzumab from January 2015 to December 2018. Patients included in the study will be followed up for survival. The main endpoint is 3-year overall survival (OS) rate; the secondary endpoint are 3-year progression-free survival (PFS) rate, 3-year Local-regional control (LRC) rate, objective response rate (ORR), disease control rate (DCR) and safety.
Study Type
OBSERVATIONAL
Enrollment
1,931
Patients in the study group were received nimotuzumab on the basis of chemoradiotherapy (control group).
Beijing Cancer Hospital
Beijing, Beijing Municipality, China
The General Hospital of the People's Liberation Army
Beijing, Beijing Municipality, China
Sun Yat-sen University Cancer Centre
Guangzhou, Guangdong, China
First Affiliated Hospital of Xi 'an Jiaotong University
Xi'an, Shannxi, China
3-year overall survival (OS) rate
3-year overall survival (OS) rate
Time frame: Up to 3 years
3-year progression-free survival (PFS) rate
3-year progression-free survival (PFS) rate
Time frame: Up to 3 years
3-year Local-regional control (LRC) rate
3-year Local-regional control (LRC) rate
Time frame: Up to 3 years
objective response rate (ORR)
objective response rate (ORR)=CR+PR
Time frame: Up to 12 months
disease control rate (DCR)
disease control rate (DCR)
Time frame: Up to 12 months
Safety as measured by number and grade of adverse events
Classification, frequency, and severity of drug-related adverse events
Time frame: Up to 3 years
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Tianjin Cancer Hospital
Tianjin, Tianjin Municipality, China