19
Participants
Start Date
November 26, 2012
Primary Completion Date
September 29, 2021
Study Completion Date
September 29, 2021
trametinib
Trametinib will be given for 5-day lead-in period by mouth daily Monday-Friday starting at day -14 through -10 and concurrently for the duration of radiation therapy (approximately days 1-38).The dose of Trametinib will be escalated: 0.5 mg, 1.0 mg, 2mg. If the 2 mg dose level causes DLT (dose-limiting toxicity)in 2 out of 6 patients and the 1mg dose level was acceptable, then a 1.5 mg dose cohort will be used.
fluorouracil
Will be administered as a continuous infusion over 120 hours at a dose of 225 mg/m2/day on Monday to Friday of every week starting day 1-38.
radiation therapy
Radiation therapy will be delivered to the pelvis during (approximately) days 1-33 (five days a week, Mondays through Fridays for 25 fractions) using a 3-field or 4-field 3-D conformal plan to the primary tumor, surrounding soft tissues, and at risk lymph node stations (peri-rectal, presacral, internal iliac, with or without external iliac) to a total dose of 45 Gy in 1.8 Gy daily fractions. A boost radiation field will be delivered during (approximately) days 36-38. The boost will encompass the primary rectal tumor and involved lymph nodes with a 2-2.5 cm margin, which should include the presacral space. The boost dose will be 5.4 Gy in 1.8 Gy fractions for a total dose of 50.4 Gy.
Roswell Park Cancer Institute, Buffalo
Vanderbilt University, Nashville
Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center, Columbus
Siteman Cancer Center at Washington University, St Louis
Collaborators (1)
National Comprehensive Cancer Network
NETWORK
Novartis Pharmaceuticals
INDUSTRY
Ohio State University Comprehensive Cancer Center
OTHER