Randomized Phase III Trial of Gemcitabine Plus Cisplatin Compared With Gemcitabine Alone in Advanced Pancreatic Cancer
Düsseldorf University Hospital · München Klinik Harlaching · +1 more institution
Abstract
PURPOSE: To compare the effectiveness and tolerability of gemcitabine plus cisplatin with single-agent gemcitabine as first-line chemotherapy for locally advanced or metastatic pancreatic cancer. PATIENTS AND METHODS: Patients with advanced adenocarcinoma of the pancreas were randomly assigned to receive either gemcitabine 1,000 mg/m2 and cisplatin 50 mg/m2 given on days 1 and 15 of a 4-week cycle (GemCis arm) or gemcitabine alone at a dose of 1,000 mg/m2 on days 1, 8, and 15 of a 4-week regimen (Gem arm). The primary end point was overall survival; secondary end points were progression-free survival, response rate, safety, and quality of life. RESULTS: One hundred ninety-five patients were enrolled and showed…
Citation impact
- FWCI
- 21.52
- Percentile
- 100%
- References
- 29
Authors
20- VHVolker HeinemannCorresponding
Düsseldorf University Hospital, München Klinik Harlaching, Heinrich Heine University Düsseldorf
- DQD. Quietzsch
Düsseldorf University Hospital, München Klinik Harlaching, Heinrich Heine University Düsseldorf
- FGFrank Gieseler
Düsseldorf University Hospital, München Klinik Harlaching, Heinrich Heine University Düsseldorf
- MGMichael Gonnermann
Düsseldorf University Hospital, München Klinik Harlaching, Heinrich Heine University Düsseldorf
- HSH Schönekäs
Düsseldorf University Hospital, München Klinik Harlaching, Heinrich Heine University Düsseldorf
Topics & keywords
- Gemcitabine
- Medicine
- Tolerability
- Regimen
- Pancreatic cancer
- Internal medicine
- Clinical endpoint
- Hazard ratio
- Good health and well-being