Proton Therapy for Stage I Non-Small Cell Lung Cancer (LU03)
LU03
Hypofractionated, Image-Guided Radiation Therapy With Proton Therapy for Stage I Non-Small Cell Lung Cancer
1 other identifier
interventional
23
1 country
1
Brief Summary
This is a research study to determine if hypofractionated image guided radiation therapy (hypoIGRT) with proton therapy is a good way to treat early stage lung tumors for patients who will not have surgery. HypoIGRT delivers higher daily doses of radiation over a shorter period of time compared with conventional radiation. This is thought to deliver a more lethal dose of radiation to the tumor and is more convenient with treatment being completed within 2-3 weeks compared to the typical 7-8 week course of conventional radiotherapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable nonsmall-cell-lung-cancer
Started Sep 2009
Longer than P75 for not_applicable nonsmall-cell-lung-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 2, 2009
CompletedFirst Posted
Study publicly available on registry
April 6, 2009
CompletedStudy Start
First participant enrolled
September 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 21, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
March 21, 2022
CompletedMarch 24, 2022
March 1, 2022
12.6 years
April 2, 2009
March 23, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Confirm Grade 3 or higher toxicity rate of hypoIGRT proton therapy in patients with stage I non-small cell lung cancer.
1 year after the end of radiation therapy
Secondary Outcomes (3)
Collect and analyze outcome data on tumor control and survival
When each patient has been followed for a minimum of 12 months to a maximum of 5 years
Assess differences in dosimetric values compared with photons for lung, heart, esophagus, spinal cord, skin and brachial plexus
When each patient has been followed for a minimum of 12 months to a maximum of 5 years
Assess changes in quality of life before and after treatment
Before treatment and then when each patient has been followed for a minimum of 12 months to a maxiumum of 5 years
Study Arms (2)
Peripherally located lung tumor
EXPERIMENTAL12 cobalt gray equivalent per fraction to a total of 48 cobalt gray equivalent
Centrally located lung tumor
EXPERIMENTAL6 cobalt gray equivalent per fraction to a total of 60 cobalt gray equivalent
Interventions
12 cobalt gray equivalent per fraction for 4 fractions, 2-3 treatments per week (every other day), over 2 weeks for a total of 48 cobalt gray equivalent (Fractions at lest 40 hours apart)
6 cobalt gray equivalent per fraction for 10 fractions, 5 treatments per week over 2-3 weeks for a total of 60 cobalt gray equivalent (no more than one fraction per calendar day)
Eligibility Criteria
You may qualify if:
- Pathologically confirmed, by biopsy or cytology, non-small cell lung carcinoma diagnosed within 3 months prior to study enrollment.
- T1, N0, M0 or T2, N0, M0. (AJCC Lung 7th Edition)
- At least 18 years old at the time of consent.
- Adequate bone marrow function.
- Medically inoperable. Medically operable candidates are allowed if they refuse surgical resection.
- If the patient has a large pleural effusion, it must be biopsy negative.
You may not qualify if:
- Evidence of distant metastasis (M1) and/or nodal involvement (N1, N2, N3).
- Synchronous primary.
- T2 tumors \> 5 cm; T3, T4 primary tumor.
- Previous radiotherapy for lung cancer.
- Concomitant local, regional, and/or systemic therapy during radiotherapy.
- Active systemic, pulmonary, and/or pericardial infection.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Florida Proton Therapy Institute
Jacksonville, Florida, 32206, United States
Related Publications (23)
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PMID: 12171836BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Romaine C Nichols, MD
University of Florida Proton Therapy Institute
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 2, 2009
First Posted
April 6, 2009
Study Start
September 1, 2009
Primary Completion
March 21, 2022
Study Completion
March 21, 2022
Last Updated
March 24, 2022
Record last verified: 2022-03