Skip to content

Concurrent Chemo-radiation Form NSCLC to a Individualized MLD

Concurrent Chemo-radiotherapy for Stage III Non-small Cell Lung Cancer ta an Individualized MLD

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00572325
Acronym
BRONC CONC MLD
Enrollment
180
Registered
2007-12-13
Start date
2006-08-31
Completion date
2009-05-31
Last updated
2010-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Keywords

radiotherapy, NSCLC, stage III non-small cell lung cancer

Brief summary

Our group has shown in a modeling study that increasing the radiation dose to pre-specified normal tissue dose constrains could lead to increased TCP with the same NTCP in patients with non-concurrent chemo-radiation. In a subsequent phase I trial, in patients receiving non-concurrent chemo-radiation we showed the safety of this approach. Here,we want to investigate its efficacy in a prospective study in patients with stage III NSCLC, who are selected for radical concurrent radiotherapy

Detailed description

Eligible patients (see below) will receive radiotherapy to the primary tumor and the initially involved mediastinal lymph nodes to the following MLD (Mean Lung Dose): * MLD=19 Gy when Fev1 and DLCO\>50% of the predicted value * MLD=15 Gy when Fev1 and/or DLCO 40-49% of the predicted value * MLD=10 Gy when Fev1 and/or DLCO \<40% of the predicted value Other dose-constrains: spinal cord max: 54 Gy, brachial plexus (Dmax):66 Gy Minimum tumor dose:54 Gy. Maximal tumor dose:69 Gy Radiotherapy will be delivered as follows: 1. First 3 weeks: 30 fractions: twice-daily fractions of 1.5 Gy, with 8 to 10 h as interfraction-interval, 5 days per week Total dose;45Gy/30 fractions 2. Thereafter: once-daily fractions of 2.0 Gy, 5 days per week until the target dose has been reached. 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 type will be registered. 2. concurrent part:(day1= first day of radiotherapy) 1. cisplatin - vinorelbine * Cisplatin 50 mg/m2 day 2 and day 9 * Vinorelbine 20 mg/m2 day 2 and day 9 * Cisplatin 40mg/m2 day 23 * Vinorelbine 15mg/m2 day 23 and day 30 2. cisplatin - docetaxel * Cisplatin 50 mg/m2 day 2,9 and 29 * Docetaxel 20 mg/m2 day 2, 9, 16, 23 and 29 3. cisplatin - etoposide * Cisplatin 60 mg/m2 day 1 * Docetaxel 120 mg/m2 day 1-3 Q 3 weeks, 3 cycles When the calculated creatinin clearance is less than 60 ml/min, cisplatin may be substituted for carboplatin

Interventions

None listed

Sponsors

Maastricht Radiation Oncology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histological or cytological proven NSCLC * UICC stage I-III * Performance status 0-2 * FeV 1 and DLCO at least 30% of the age-predicted value

Exclusion criteria

* Not NSCLC or mixed NSCLC and other histologies (e.g. small cell carcinoma) * UICC stage IV * Performance status 3 or more * FeV 1 and DLCO \< 30% of the age-predicted value

Design outcomes

Primary

MeasureTime frame
death2,3 and 5 years

Secondary

MeasureTime frame
-progression-free interval -Dyspnea (CTCAE 3.0) -Dysphagia (CTCAE 3.0) -Patterns of recurrence2,3 and 5 years

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 30, 2026