Image-Guided Hypofractionated Radiation Therapy With Stereotactic Body Radiation Therapy Boost and Combination Chemotherapy in Treating Patients With Stage II-III Non-Small Cell Lung Cancer That Cannot Be Removed By Surgery
NCT01345851 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 29
Last updated 2026-02-25
Summary
This clinical trial studies image-guided hypofractionated radiation therapy (RT) when given together with hypofractionated RT boost and combination chemotherapy in treating patients with stage II-III non-small cell lung cancer (NSCLC) that cannot be removed by surgery. RT uses high energy x-rays to kill tumor cells. Hypofractionated RT may be able to send x-rays directly to the tumor and cause less damage to normal tissue. Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving RT together with combination chemotherapy may kill more tumor cells and allow doctors to save the part of the body where the cancer started
Conditions
- Adenocarcinoma of the Lung
- Adenosquamous Cell Lung Cancer
- Large Cell Lung Cancer
- Recurrent Non-small Cell Lung Cancer
- Squamous Cell Lung Cancer
- Stage IIA Non-small Cell Lung Cancer
- Stage IIB Non-small Cell Lung Cancer
- Stage IIIA Non-small Cell Lung Cancer
- Stage IIIB Non-small Cell Lung Cancer
Interventions
- RADIATION
-
hypofractionated radiation therapy
Undergo image-guided hypofractionated Radiation Therapy over 35 minutes 5 days a week for 2 weeks
- OTHER
-
laboratory biomarker analysis
Correlative studies
- RADIATION
-
image-guided radiation therapy
Undergo 5 fractions of image-guided hypofractionated Radiation Therapy boost.
- DRUG
-
The maximal chemotherapy treatment dose for carboplatin during the 3 week radiation therapy is AUC 2.
- DRUG
-
The maximal chemotherapy treatment dose for paclitaxel during the 3 week radiation therapy is 45mg/m2.
- RADIATION
-
stereotactic body radiation therapy
Undergo hypofractionated RT
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Jonsson Comprehensive Cancer Center
lead OTHER
Principal Investigators
-
Percy Lee · Jonsson Comprehensive Cancer Center
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-03-23
- Primary Completion
- 2027-01-31
- Completion
- 2028-01-31
Countries
- United States
Study Locations
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