Significance of Chemoradiation Following Induction Chemotherapy in Locally Advanced,Unresectable Pancreatic Cancer -a Randomised Phase 3 Trial: Chemoradiation Following Induction Chemotherapy Compared With Chemotherapy Alone

Who is this study for? Patients with locally advanced unresectable pancreatic cancer
Status: Completed
Location: See all (23) locations...
Intervention Type: Drug, Radiation
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This randomized trial examines the effectiveness of chemoradiotherapy compared to chemotherapy alone after induction chemotherapy with 3 cycles of gemcitabine or 6 cycles of FOLFIRINOX in patients with locally advanced, non resectable and non-metastatic pancreatic cancer. Chemotherapeutic agent in chemoradiotherapy is gemcitabine administered in 5 cycles, the agent and its administration for sole chemotherapy is determined by induction chemotherapy. Operability of tumor is evaluated at week 11 after randomisation. Patients will be followed for the duration of therapy and for 5 years after the last study treatment. Overall survival at the end of follow up is defined as primary endpoint. Secondary endpoints are tumor-free survival, rate of local recurrence or local progression, rate of distant metastasis, acute and late toxicity of the chemoradiotherapy, quality of life, rate of remission, rate of curative resections (R0) after chemotherapy and chemoradiotherapy. It is planned to include a total number of 830 patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \> 18 years

• histologically confirmed adenocarcinoma of the pancreas

• no evidence of distant metastasis based on computed tomography of the thorax and abdomen

• non resectable pancreatic cancer

• no evidence of peritoneal carcinosis

• ECOG-performance status ≤ 2

• signed study-specific consent form prior to therapy

Locations
Other Locations
Germany
Bayreuth, Klinikum
Bayreuth
Bochum, Augusta-Kranken-Anstalt, Hämatologie/Onkologie
Bochum
Bochum, St. Josef-Hospital
Bochum
Dresden Onkologische Gemeinschaftspraxis
Dresden
Erlangen Universitätsklinikum
Erlangen
Frankfurt/Main Universitätsklinikum
Frankfurt/main
Freiburg Universitätsklinikum
Freiburg
Göttingen Universitätsmedizin
Göttingen
Halle St. Elisabeth und St. Barbara Krankenhaus
Halle/saale
Heilbronn SLK-Kliniken
Heilbronn
Jena Universitätsklinikum
Jena
Köln Universitätsklinikum
Köln
Leer MVM
Leer
Leipzig UCCL
Leipzig
Magdeburg Klinikum
Magdeburg
Magdeburg Universitätsklinikum
Magdeburg
Mannheim Universitätsmedizin
Mannheim
München Großhadern LMU
München
Münster Universitätsklinikum
Münster
Oldenburg Pius Hospital
Oldenburg
Regensburg Krankenhaus Barmherzige Brüder
Regensburg
Regensburg Universitätsklinikum
Regensburg
Würzburg CCC Mainfranken
Würzburg
Time Frame
Start Date: 2013-04-04
Completion Date: 2023-11-08
Participants
Target number of participants: 830
Treatments
Experimental: Induction CT, chemoradiotherapy
Induction chemotherapy with gemcitabine or FOLFIRINOX; Radiotherapy, 28 x 1.8 Gy; Chemotherapy, gemcitabine;
Active_comparator: Induction CT, chemotherapy
Induction chemotherapy with gemcitabine or FOLFIRINOX; Chemotherapy with gemcitabine or FOLFIRINOX according to induction chemotherapy
Related Therapeutic Areas
Sponsors
Leads: University of Erlangen-Nürnberg Medical School

This content was sourced from clinicaltrials.gov