This trial is a retrospective, observational study, patients who underwent surgical resection of the pancreas for non-metastatic pancreatic cancer between 2016 and 2022 were selected and divided into two groups according to with (study arm) or without (control arm) nimotuzumab. The primary efficacy endpoint was overall survival (OS).
This trial is a retrospective, observational study based on real-world data obtained from the Health Information System (HIS) of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine. Patients who underwent surgical resection of the pancreas for non-metastatic pancreatic cancer between 2016 and 2022 were selected and divided into two groups according to with (study arm) or without (control arm) nimotuzumab. The primary efficacy endpoint was overall survival (OS).
Study Type
OBSERVATIONAL
Enrollment
64
Nimotuzumab (400mg) was given weekly
overall survival (OS)
The primary endpoint is overall survival (OS), defined as the time from the start of surgery to the date of death due to any cause.
Time frame: approximately 84 months
disease-free survival (DFS)
DFS is defined as the time from surgical resection to the first tumor recurrence/progression or death due to any cause.
Time frame: approximately 84 months
locoregional recurrence-free survival (LRRFS)
LRRFS is defined as the time from surgical treatment to clinically or radiographically confirmed local recurrence and/or regional progression at follow-up.
Time frame: approximately 84 months
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