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RECRUITING
NCT07632079
PHASE2

Hypofractionated Definitive Chemoradiotherapy for Oesophageal Cancer

Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

View on ClinicalTrials.gov

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

RADIATION

Hypofractionation

20 fractions of 2.4 Gy

DRUG

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