Clinical Trials Directory

Trials / Completed

CompletedNCT01166204

Concurrent and Non-concurrent Chemo-radiotherapy or Radiotherapy Alone With Intensity-modulated Radiotherapy (IMRT) for Non Small Cell Lung Cancer (NSCLC) to an Individualised Mean Lung Dose (MLD)

Concurrent and Non-concurrent Chemo-radiotherapy or Radiotherapy Alone With IMRT for Stage I-III Non-small Cell Lung Cancer to an Individualised MLD

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

Summary

Our group has shown that increasing the radiation dose to pre-specified normal tissue dose constraints could lead to increased TCP with the same NTCP in patients with non-concurrent and concurrent chemo-radiation. Here, the investigators want to investigate its efficacy in a prospective study in patients with stage I-III NSCLC, who are selected for high-dose radiotherapy with or without chemotherapy, but treated with IMRT. The latter technique has become standard, but the patterns of recurrence and the possibility for dose-escalation in an individualised setting have never been investigated properly.

Detailed description

Eligible patients (see below) will receive radiotherapy to the primary tumor and the initially involved mediastinal lymph nodes to an MLD (Mean Lung Dose) of 20 +/-1Gy, irrespective of lung function. Other dose-constraints: spinal cord max: 54Gy, brachial plexus (Dmax):66Gy In concurrence with chemotherapy, radiotherapy will be delivered as follows: * First three weeks/30 fractions: twice-daily fractions of 1.5Gy, with 8h to 10h as interfraction interval, 5 days per week. Total dose: 45Gy/30 fractions * Thereafter: once daily fractions of 2.0Gy, 5 days per week until the target dose has been reached. In sequential or radiotherapy alone schedules, twice-daily 1.8Gy with an interfraction interval of at least 8h will be delivered. The radiation doses will be specified according to ICRU 50. Lung density corrections will be applied, as well as all standard QA procedures. Technical requirements are the same as in standard practice at MAASTRO clinic Chemotherapy schedules allowed: 1. 1-2 cycles induction chemotherapy: any third generation schedule is allowed. The type will be registered. 2. Concurrent part: (day 1 = first day of radiotherapy) * cisplatin - vinorelbine * cisplatin - docetaxel * cisplatin - etoposide * cisplatin - pemetrexed in non-squamous histologies Q 3 weeks; 3 cycles When the calculated creatinin clearance is less than 60ml/min, cisplatin may be substituted for carboplatin

Conditions

Interventions

TypeNameDescription
RADIATIONRadiotherapyRadiotherapy

Timeline

Start date
2009-05-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2010-07-20
Last updated
2017-05-23

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01166204. Inclusion in this directory is not an endorsement.