Pancreatic Adenocarcinoma Clinical Trial
— Net-PacOfficial title:
Neoadjuvant Radiotherapy in Patients With Primary Resectable Adenocarcinoma of the Pancreatic Head Plus Adjuvant Chemotherapy: a Randomized Controlled Phase III Trial
Verified date | July 2015 |
Source | CHIR-Net |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Federal Office for Radiation Protection |
Study type | Interventional |
Net-Pac investigates if radiation prior to surgical resection improves survival in patients with pancreatic head cancer without metastases.
Status | Terminated |
Enrollment | 5 |
Est. completion date | October 2014 |
Est. primary completion date | October 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Histologically confirmed adenocarcinoma of the pancreatic head - Age = 18 years - Signed informed consent - ECOG performance status of 0-2 Exclusion Criteria: - Curative resection is not feasible or presence of metastatic disease - Patients not eligible for surgery (ASA = 4) - Participation in an other clinical trial - Unable or unwilling to sign the informed consent |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | Klinikum rechts der Isar, Technische Universität München | Munich |
Lead Sponsor | Collaborator |
---|---|
CHIR-Net | Technische Universität München |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Local recurrence free survival | At 12 months postoperative | No | |
Secondary | Percentage of surgical R0-resections in both groups | Determined by histopathological analysis of the surgical specimen. | Until 10 days postoperative | No |
Secondary | 30-day morbidity and mortality | 30 day period after the operation | Yes | |
Secondary | Toxicity of preoperative Radiotherapy | Number of patients with adverse events in both groups, number of adverse events in both groups and number of grade 3 and 4 adverse events according to the Common Terminology Criteria for Adverse Events version 3.0 (CTCAE v 3.0) in both groups | Start of the radiotherapy until 12 months postoperative. | Yes |
Secondary | Clinical response rate (RECIST-criteria) and histological response rate | Until 1 year postOP | Yes | |
Secondary | Time to tumor progression (local and systemic) | Until 1 year postoperative | No | |
Secondary | Quality of life | Until 12 months postoperative | Yes | |
Secondary | Overall survival after 1 year | Until 1 year postoperative | Yes |
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