RecruitingPhase 1NCT06080061
Personalized Accelerated ChEmoRadiation (PACER) for Lung Cancer
Phase I Trial of Personalized Accelerated ChEmoRadiation (PACER) for Lung Cancer
Sponsor
Stanford University
Enrollment
45 participants
Start Date
Oct 25, 2023
Study Type
INTERVENTIONAL
Conditions
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.
Eligibility
Min Age: 18 Years
Inclusion Criteria5
- Histologically or cytologically documented malignancy of the lung including non-small cell lung cancer or small cell lung cancer planned for definitive therapy with fractionated radiation (60-66 Gy) and concurrent systemic therapy
- ECOG performance status of 0-2
- Age \> 18 years old
- Ability to understand and the willingness to personally sign the written IRB approved informed consent document
- Estimated life expectancy of 12 weeks or longer
Exclusion Criteria5
- Contraindication to receiving radiotherapy or systemic therapy as determined by treating radiation and medical oncologist
- Age \< 18 years old
- Tumor directly invading the major pulmonary arteries, aorta, heart or proximal bronchial tree
- Diagnosis of interstitial pulmonary fibrosis
- Previous radiation therapy to the thorax that would result in overlapping high dose radiation fields
Interventions
RADIATIONHypofractionated accelerated radiation therapy
Hypofractionated accelerated radiation therapy
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06080061
Related Trials
Virtual Agent Feasibility in Oncology Patients (NTT Data)
NCT066820131 location
A Trial of RSC-1255 for Treatment of Patients With Advanced Malignancies
NCT046786483 locations
Study of Novel Treatment Combinations in Patients With Lung Cancer
NCT05633667100 locations
Lung Cancer Screening in HIgh Risk nonsmokErs by Artificial inteLligence Device
NCT062954971 location
A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors
NCT0661828763 locations