Clinical Trials Directory

Trials / Completed

CompletedNCT00181506

HI-CHART:Feasibility of High-Dose Accelerated Conformal Radiotherapy

HI-CHART: A Phase I/II Study on the Feasibility of High-Dose Accelerated Conformal Radiotherapy in Patients With Inoperable Non-Small Cell Lung Cancer.

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
180 (planned)
Sponsor
Maastricht Radiation Oncology · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this study we try to increase the radiation dose, while reducing or keeping the radiation schedule below 4 weeks. The study hypothesis is that it is feasible to administer hyperfractionated accelerated radiotherapy to patients with inoperable or locally advanced non small cell lung cancer.

Detailed description

Non-small cell lung cancer is still the most common cancer and the main cause of cancer death. Treatment of choice for these patients is often radiotherapy, which results in an overall 5-year survival rate between 5 and 10%. The addition of chemotherapy improves survival by a few percentages and is therefore considered standard treatment for patients with stage III disease. However, several factors have been identified that have an impact on the local control but also on survival. 1. There is a dose-effect relationship. A higher dose results in a better survival rate. However, higher radiation doses are currently not delivered with conventional radiation due to the tolerance of normal tissue. 2. The time factor plays an important role in radiotherapy. Prolonging the overall treatment time decreases the outcome of radiotherapy. Radiobiological modelling of data shows that the overall treatmetn time (OTT) should be kept below 4 weeks. Results from studies support this conclusion. So, probably the best results will be achieved when a very high radiation dose can be delivered within 4 weeks, without severally damaging normal tissue. In order to achieve this goal, an hyperfractionated accelerated treatment regimen together with a technically very advanced radiation technique to avoid as much normal tissue as possible, will be used in this study.

Conditions

Interventions

TypeNameDescription
PROCEDUREdose escalation (radiotherapy treatment schedule)

Timeline

Start date
2001-12-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2005-09-16
Last updated
2009-06-30

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00181506. Inclusion in this directory is not an endorsement.