RECRUITING

Stereotactic Magnetic Resonance Guided Radiation Therapy

Description

This is a master prospective Phase I-II trial evaluating feasibility and efficacy of stereotactic magnetic resonance (MR) guided adaptive radiation therapy (SMART) in patients with cancer. * The phase 1 study will evaluate the feasibility and safety of delivering SMART in patients with cancer. * Phase 2 will evaluate efficacy of SMART with specific reference to tumor control and improvement in patient reported outcome measures

Study Overview

Study Details

Study overview

This is a master prospective Phase I-II trial evaluating feasibility and efficacy of stereotactic magnetic resonance (MR) guided adaptive radiation therapy (SMART) in patients with cancer. * The phase 1 study will evaluate the feasibility and safety of delivering SMART in patients with cancer. * Phase 2 will evaluate efficacy of SMART with specific reference to tumor control and improvement in patient reported outcome measures

A Master Protocol of Stereotactic Magnetic Resonance Guided Adaptive Radiation Therapy (SMART)

Stereotactic Magnetic Resonance Guided Radiation Therapy

Condition
Pancreas Cancer
Intervention / Treatment

-

Contacts and Locations

Boston

Brigham & Women's Hospital, Boston, Massachusetts, United States, 02115

Boston

Dana Farber Cancer Institute, Boston, Massachusetts, United States, 02115

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Participants must have a confirmed malignancy requiring stereotactic body radiation therapy. See specific disease site cohorts for more details.
  • * Tumor size ≤ 7cm
  • * Age 18 years of older.
  • * ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A)
  • * Ability to understand and the willingness to sign a written informed consent document.
  • * Specific eligibility requirements for each disease site with be covered in each specific cohort.
  • * Specific exclusion requirements for each disease site with be covered in each specific cohort
  • * History of allergic reactions attributed to gadolinium-based IV contrast.
  • * Pregnant women are excluded from this study.
  • * Severe claustrophobia or anxiety
  • * Participants who cannot undergo an MRI

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Dana-Farber Cancer Institute,

Jonathan Leeman, MD, PRINCIPAL_INVESTIGATOR, Brigham and Women's Hospital

Study Record Dates

2028-06