Non-Small Cell Lung Cancer
Conditions
Brief summary
The aims of the study are to reduce acute radiation induced side effects, i.e. pneumonitis and esophagitis grade II or higher by the use of proton therapy compared to photon radiotherapy of equal total dose. Secondary endpoints include evaluation of quality of life, loco-regional control, survival and late radiation induced side effects.
Detailed description
Patients in this trial undergo primary radiochemotherapy for locally advanced NSCLC. As early and intermediate late effects of radiotherapy do not only hamper quality of life but can, in the case of radiation induced pneumonitis, be potentially lethal, a reduction of these side effects is desirable. Patients in this trial are 1:1 randomised to intensity modulated radiotherapy with photons or proton therapy. The primary aim of the study is to show a decrease of pneumonitis and or esophagitis grade 2 or higher by proton therapy. The observed incidence of both these side effects is 39% with photon therapy. The estimated incidence with proton therapy is around 12 %. Simultaneous chemotherapy will be applied to current clinical standards.
Interventions
RADIATIONProton therapy
RADIATIONPhoton therapy
Sponsors
German Cancer Research Center
National Center for Radiation Research in Oncology Dresden/Heidelberg
Technische Universität Dresden
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* NSCLC (confirmed by cytology or histology) staged UICC IIIA or IIIB or UICC II if the patient declines surgery * no distant metastases (M1) * patient' age between 18 and 70 years * Patient medically suited for primary radiochemotherapy with curative intent * signed declaration of informed consent * adequate compliance for treatment and clinical follow up * adequate contraception during and after therapy if indicated
Exclusion criteria
* Participation in other interventional trial * T1 or T2 N0 tumours that are candidates for stereotactic radiotherapy * relevant neurological or psychiatric disorders that hinder treatment, follow-up or understanding of the procedures * pregnant or breastfeeding women * prior thoracic radiotherapy * history of other malignancies during the last 5 years (exceptions can be made for tumours with excellent outcome) * weight loss greater than 15% before therapy * serological alterations (liver, kidney) prohibiting application of simultaneous chemotherapy * respiratory motion of the tumour \> 10 mm (evaluated by 4D CT), also when methods for motion reduction (abdominal compression) are used
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of acute and intermediate radiation induced side effects | no later than six months after end of treatment |
Countries
Germany
Contacts
Primary ContactEsther Troost, Prof.
Outcome results
None listed