Phase I Trial of Personalized Accelerated ChEmoRadiation (PACER) for Lung Cancer
Summary
The purpose of this study is to examine the use of hypofractionated accelerated radiation therapy (HART) to treat locally advanced lung cancer. Depending on the location and size of the tumor.
Arms & interventions
- RadiationHypofractionated accelerated radiation therapy
Hypofractionated accelerated radiation therapy
Outcome measures
Primary
Dose limiting pulmonary and esophageal toxicity
Toxicities will be scored by the CTCAE v5.0 criteria. Specific toxicities evaluated are grade 2+ pneumonitis and grade 3+ esophagitis as well as other G3+ pulmonary, esophageal or cardiac toxicities that could be probably or definitely attributed to rT.
Time frame: 9 months
Secondary
Acute and Late Toxicities
Time frame: 36 months
Integrated adaptive dosing regimen with an automated planning system
Time frame: 36 months
Progression free survival
Time frame: 36 months
Overall survival
Time frame: 36 months
Local control
Time frame: 36 months
Eligibility criteria
Study locations (2)
Stanford University
Palo Alto, California, 94305
Stanford Cancer Center South Bay
San Jose, California, 95124