Palliative Short-course Hypofractionated Radiotherapy Followed by Chemotherapy in Adenocarcinoma of the Esophagus or Esophagogastric Junction Trial - a Phase II Clinical Trial Protocol.

Status: Completed
Location: See location...
Intervention Type: Radiation, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

In this trial, patients with histologically proven adenocarcinoma of the esophagus or esophagogastric junction noneligible for surgery or chemoradiation with curative intent will be included. Primary objective is to determine the rate of improvement in dysphagia after palliative short course hypofractionated radiotherapy (5 x 4 Gy) followed by chemotherapy consisting of oxaliplatin and fluorouracil. The rate of improvement of dysphagia is evaluated by a 5 graded dysphagia score, and a positive change of at least 1 score is considered to be an improvement.

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

• Patients with histologically proven adenocarcinoma of the esophagus or esophagogastric junction noneligible for surgery or chemoradiation with curative intent

• Any T, N and M

• Age: 18 years or older

• WHO performance status ≤ 2

• Life expectancy \> 3 months

• Dysphagia score \> 0

• Adequate laboratory findings: hemoglobin \> 90 g/L, absolute neutrophil count

⁃ 1.0 10 9/L, platelets ≥ 75 x 10 9/L, bilirubin ≤ 1.5 x upper limit of normal (ULN), alanine aminotransferase (ALAT) ≤ 5 x ULN, creatinine ≤ 1.5 x ULN

• Fertile men and women must use effective means of contraception

• Signed written informed concent

• The patient must be able to comply with the protocol

Locations
Other Locations
Sweden
Lund University Hospital, Department of Oncology
Lund
Time Frame
Start Date: 2014-10
Completion Date: 2019-05
Participants
Target number of participants: 29
Treatments
Experimental: Radiotherapy and chemotherapy (oxaliplatin and fluorouracil).
Radiotherapy (5 x 4 Gy) will be given. After completion of radiotherapy, 4 cycles of chemotherapy will be administered, cycle length 14 days. Each patient will receive oxaliplatin as infusion at a dose of 85 mg/m2, followed by a bolus injection of fluorouracil at a dose of 400 mg/m2, and a long time infusion (44 hours) of fluorouracil at a dose of 2 400 mg/m2.
Authors
Related Therapeutic Areas
Sponsors
Leads: Lund University Hospital

This content was sourced from clinicaltrials.gov