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Spots Global Cancer Trial Database for Neoadjuvant Treatment in Resectable Pancreatic Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Neoadjuvant Treatment in Resectable Pancreatic Cancer

Official Title: Sequential Neoadjuvant Chemoradiotherapy (CRT) Followed by Curative Surgery vs. Primary Surgery Alone for Resectable, Non-metastasized Pancreatic Adenocarcinoma

Study ID: NCT01900327

Study Description

Brief Summary: Sequential Neoadjuvant Chemoradiotherapy (CRT) Followed by Curative Surgery vs. Primary Surgery Alone for Resectable, Non-metastasized Pancreatic Adenocarcinoma

Detailed Description: Median overall-survival (OS) after surgery in curative intent for non-metastasized pancreas cancer ranges under study conditions from 17.9 months to 23.6 months. Tumor recurrence occurs locally, at distant sites (liver, peritoneum, lungs), or both. Observational and autopsy series report local recurrence rates of up to 87% even after potentially "curative" R0 resection. To achieve better local control, neoadjuvant chemo-radiation therapy (CRT) has been suggested for preoperative tumour downsizing, to elevate the likelihood of curative, margin-negative R0 resection and to increase the OS rate. However, controlled, randomized trials addressing the impact of neoadjuvant CRT survival do not exist. The underlying hypothesis of this randomized, two-armed, open-label, multicenter, phase III trial is that neoadjuvant CRT increases the three-year overall survival by 12% (30% to 42%) compared to patients undergoing upfront surgery for resectable pancreatic cancer. Overall, 410 patients (n=205 in each study arm) will be enrolled in the trial, taking into regard an expected drop out rate of 7% and allocated either to receive neoadjuvant CRT prior to surgery or to undergo surgery alone. Circumferential resection margin status, i.e. R0 and R1 rates, respectively, surgical resectability rate, local and distant disease-free and global survival, and first site of tumor recurrence constitute further essential endpoints of the trial.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University Freiburg, Freiburg, Baden-Württemberg, Germany

Heidelberg University, Heidelberg, Baden-Württemberg, Germany

Technische Universität München, München, Bayern, Germany

University Regensburg, Regensburg, Bayern, Germany

Klinikum Augsburg, Augsburg, Bayer, Germany

Klinikum Darmstadt, Darmstadt, Hessen, Germany

University of Rostock, Rostock, Mecklenburg-Vorpommern, Germany

Hannover Medical School, Hannover, Niedersachsen, Germany

St. Joseph Hospital Bochum, Bochum, Nordrhein-Westfalen, Germany

Saarland University, Homburg, Saarland, Germany

University of Schleswig-Holstein Kiel, Kiel, Schleswig-Holstein, Germany

University of Schleswig-Holstein Lübeck, Lübeck, Schleswig-Holstein, Germany

Klinikum Gera, Gera, Thüringen, Germany

University of Jena, Jena, Thüringen, Germany

University Medical Center Hamburg-Eppendorf, Hamburg, , Germany

Klinikum Karlsruhe, Karlsruhe, , Germany

Contact Details

Name: Jakob R Izbicki, MD, FACS

Affiliation: Universitätsklinikum Hamburg-Eppendorf

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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