Selective Treatment With Magnetic Resonance Image Guided Pelvic Adaptive Radiation Therapy Combined With Total Neoadjuvant ChemoTherapy for the Conservative Management of Locally Advanced Rectal Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug, Radiation
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The purpose of this research study is to find out how safe and effective is treating patients with locally advanced rectal cancer (LARC) with chemotherapy first and then follow with radiation therapy to a higher dose than what is usually delivered and see if patients could have complete response and be spared from surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with newly diagnosed, biopsy proven, rectal adenocarcinoma.

• Primary tumor located ≤18 cm from margin verge.

• Primary tumor either a T3N0 or T1-4 N positive (as defined per pelvic MRI; nodes ≤ 15 mm).

• ≥ 18 years of age.

• Eastern Cooperative Oncology Group (ECOG) performance status 0-2.

• Serum liver function tests values within the range of 1.5 x Upper Limit of Normal (within 6 weeks of enrollment).

• Negative pregnancy test for women of child-bearing potential (within 4 weeks of enrollment).

• Ability to understand and the willingness to sign a written informed consent document.

• Patient is assessed by a surgeon, medical oncologist and a radiation oncologist and deemed fit for Total Neoadjuvant ChemoTherapy (TNT) and surgery.

Locations
United States
Florida
University of Miami
RECRUITING
Miami
Contact Information
Primary
Zuzel Rodriguez
z.rodriguez1@med.miami.edu
305-243-0124
Time Frame
Start Date: 2022-10-05
Estimated Completion Date: 2027-10-31
Participants
Target number of participants: 25
Treatments
Experimental: SMART TNT Plan I
Participants will initiate therapy with neoadjuvant chemotherapy of either six (6) 14-day cycles of 5-fluorouracil + leucovorin + oxaliplatin (FOLFOX), six (6) 14-day cycles of 5-fluorouracil + leucovorin + irinotecan + oxaliplatin (mFOLFIRINOX), or four (4) 21-day cycles of capecitabine+oxaliplatin (CAPOX). Participants will then receive chemo-radiation therapy according to Plan I as follows:~Plan I (5 weeks):~* MRI-guided pelvic IMRT to the Planning Tumor Volume (PTV) at a dose of 50 Grays (gy) delivered in 25 fractions (fx) over 5 weeks.~* Concurrent chemotherapy beginning on Day 1 of RT either:~ * 5-FU delivered 5 or 7 days per week.~ * Capecitabine (Xeloda) delivered 5 days per week.~After completing Plan I, participants achieving complete Clinical Response (cCR) after completing Plan I chemo-radiation will forgo the Plan II boost and continue to follow-up. Participants not achieving cCR will begin Plan II, one week after completing Plan I.
Experimental: SMART TNT Plan II
Plan II boost RT (1 week): For participants not achieving cCR after chemo-radiation. Participants will receive MRI-guided accelerated radiation therapy (ART) boost to the primary tumor.~Participants achieving a cCR will continue to follow-up. Participants still showing residual tumor will undergo standard of care treatment including surgery and adjuvant chemotherapy per institutional guidelines during follow-up.
Related Therapeutic Areas
Sponsors
Leads: University of Miami

This content was sourced from clinicaltrials.gov