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Hypofractionated Definitive Chemoradiotherapy for Oesophageal Cancer
Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Summary
The goal of this clinical trial is to learn if hypofractionation of definitive chemoradiotherapy can treat patients with locally advanced esophageal cancer. The main question it aims to answer is if this treatment is feasible and safe. We also want to investigate the toxicity, in particular the radiation-induced lymphopenia. Normally, definitive chemoradiotherapy for patients with locally advanced esophageal cancer consist of 28 fractions of 1.8 Gy with concurrent 6 cycles of carboplatin and paclitaxel in 5.5 weeks. In this study, participants will receive 20 fractions of 2.4 Gy with concurrent 6 cycles of carboplatin and paclitaxel in 4 weeks. The follow-up will be conform standard-of-care.
Official title: HYpofractionated Definitive chemoRadiotherapy for Oesophageal Cancer (HYROC): a Multicenter Phase II Feasibility Study
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2026-04-28
Completion Date
2028-07
Last Updated
2026-06-08
Healthy Volunteers
No
Interventions
Hypofractionation
20 fractions of 2.4 Gy
carboplatin + paclitaxel (CP)
6 cycles of carboplatin (AUC 2) and paclitaxel (50 mg/m2) given every 4-5 days, 6 cycles in total in 4 weeks.
Locations (7)
Amsterdam UMC
Amsterdam, Netherlands
Gelre Ziekenhuizen
Apeldoorn, Netherlands
Radiotherapiegroep
Apeldoorn, Netherlands
UMCG
Groningen, Netherlands
Zuyderland Medisch Centrum
Heerlen, Netherlands
Maastro
Maastricht, Netherlands
Radboud UMC
Nijmegen, Netherlands