This is a retrospective, multicenter, non-interventional study for the evaluation of real-world efficacy and safety of ramucirumab plus paclitaxel in gastric or gastroesophageal junction adenocarcinoma as part of the establishment of hospital medical record collection system to evaluate drug effectiveness by Health Insurance Review \& Assessment Service (HIRA). The medical records in approximately 1400 patients with locally-advanced unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma, who have received ramucirumab plus paclitaxel combination therapy will be collected.
Ramucirumab plus paclitaxel combination therapy has shown a survival benefit in patients with previously treated gastric or gastroesophageal junction adenocarcinoma. However, the real-world efficacy and safety of ramucirumab plus paclitaxel combination therapy in Korea have only been evaluated once outside of controlled clinical trials. Therefore, this large multicenter retrospective analysis was designed to evaluate the real-world efficacy and safety of ramucirumab plus paclitaxel under the Korea National Health Insurance System. The medical records in approximately 1400 patients with locally-advanced unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma, who have received ramucirumab plus paclitaxel combination therapy between May 2018 and December 2018 will be collected. Eligibility criteria included age ≥ 19 years, histologically or cytologically confirmed gastric or gastroesophageal junction adenocarcinoma, locally advanced unresectable or metastatic disease, and previous first-line systemic therapy including fluoropyrimidine and platinum. Efficacy was evaluated by overall survival, progression free survival, time to progression, objective response rate, disease control rate, and duration of response. Safety was evaluated by hematologic or non-non hematologic toxicities and adverse events of special interest with ramucirumab plus paclitaxel combination therapy.
Study Type
OBSERVATIONAL
Enrollment
1,063
Korea University Ansan Hospital
Ansan, South Korea
Hallym University Sacred Heart Hospital
Anyang, South Korea
Soonchunhyang University Bucheon Hospital
Bucheon-si, South Korea
The Catholic University of Korea, Bucheon ST. Mary's Hospital
Bucheon-si, South Korea
Dongnam Institute of Radiological&Medical Sciences
Busan, South Korea
Overall survival
Time from the start of ramucirumab plus paclitaxel to death from any cause
Time frame: Until September 30, 2019
Progression free survival
Time from the start of ramucirumab plus paclitaxel to disease progression or death from any cause
Time frame: Until September 30, 2019
Incidence of adverse events
Number (percentage) of subjects reporting adverse events
Time frame: Until September 30, 2019
Time to progression
Time from the start of ramucirumab plus paclitaxel to disease progression
Time frame: Until September 30, 2019
Objective response rate
The proportion of subjects confirmed complete or partial response
Time frame: Until September 30, 2019
Disease control rate
The proportion of subjects confirmed complete or partial response or stable disease
Time frame: Until September 30, 2019
Duration of response
Time from documentation of tumor response to disease progression
Time frame: Until September 30, 2019
Adverse events of special interest
Number (percentage) of subjects reporting adverse events of special interest associated with ramucirumab plus paclitaxel
Time frame: Until September 30, 2019
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Inje University Busan Paik Hospital
Busan, South Korea
Dong-A University Hospital
Busan, South Korea
Pusan National University Hospital
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Kosin University Gospel Hospital
Busan, South Korea
Samsung Changwon medical center
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