MRI-guided radiation therapy for rectal cancer organ preservation

MRI-Guided Adaptive Radiation Therapy for Organ Preservation in Rectal Cancer

This study is testing a new type of MRI-guided radiation therapy for people with advanced rectal cancer to see if it can safely preserve their organs while treating the disease.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 22 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Medical College of Wisconsin (Academic / other)
• Drugs / interventions: chemotherapy, Radiation
• Locations: 1 site (Milwaukee, Wisconsin)
• Trial ID: NCT04808323 on ClinicalTrials.gov

What this trial studies

This phase I clinical trial evaluates the safety and efficacy of real-time adaptive MRI-guided radiation therapy for patients with locally advanced rectal adenocarcinoma. The study aims to determine the maximum-tolerated dose of radiation while focusing on organ preservation. Participants will receive escalating doses of radiation therapy, with careful monitoring for dose-limiting toxicities. The trial includes three cohorts, each receiving different radiation doses tailored to the tumor and surrounding tissues.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18 and older with pathologically confirmed stage I-III rectal adenocarcinoma and no significant metastatic disease.

Not a fit: Patients with advanced metastatic rectal cancer or those with an ECOG status greater than 2 may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could enhance organ preservation in rectal cancer patients while minimizing treatment-related toxicity.

How similar studies have performed: While there are limited studies on adaptive MRI-guided radiation therapy for rectal cancer, similar approaches in other cancers have shown promising results, making this a potentially novel and impactful investigation.

Eligibility criteria

Inclusion Criteria:

1. Age ≥ 18.
2. Pathologically confirmed (histologic or cytological), adenocarcinoma of the rectum.
3. Determined on staging evaluation to be clinical stage I, II or III.
4. No concerning unequivocal or biopsy-proven metastatic disease. Patients are eligible with either no evidence of distant metastatic disease, or "equivocal" evidence of distant metastatic disease, as judged by the multidisciplinary tumor board. This "equivocal" definition can include small lung or liver lesions that are not able to be radiographically characterized otherwise.
5. Eastern Cooperative Oncology Group (ECOG) status 0-2 within 45 days of study entry.
6. History/physical examination, including collection of weight and vital signs within 45 days prior to start of treatment.
7. MR of the rectum is mandatory for staging and follow-up.
8. Chest CT scan within 45 days prior to study entry.
9. Radiation treatment planning abdominal CT. A mandatory pelvic MR will be done as a simulation (SIM) (ideally with interpretation). The CT SIM will not be done with interpretation. Ability to undergo abdominal MR scans for staging and radiation planning and follow-up is mandatory.
10. Laboratory values (CBC, Chem24) 45 days prior to treatment as follows:

    1. Carcinoembryonic antigen (CEA) (any value).
    2. Absolute neutrophil count (ANC) ≥ 1,000 cells/mm3.
    3. Platelets ≥50,000 cells/mm3.
    4. Hemoglobin ≥ 8.0 g/dl. (Note: The use of transfusion or other intervention to achieve Hgb ≥ 8.0 g/dl is acceptable.)
    5. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \< 4 x upper limit of normal.
    6. Total bilirubin \< 2 x upper normal mg/dL.
    7. Alkaline phosphatase \< 4 x upper limit of normal.
11. Not on hemodialysis.
12. Ability to swallow oral medications.
13. Patients must be determined by medical oncology to be a candidate for systemic chemotherapy.
14. Patients must provide study-specific informed consent prior to study entry.
15. Negative serum pregnancy test (if applicable).
16. Women of childbearing potential and male participants who are sexually active must practice adequate contraception.

Exclusion Criteria:

1. Biopsy-proven distant metastatic disease or high clinical concern for metastatic disease and tumor conference consensus of stage IV disease.
2. Prior invasive malignancy (except nonmelanomatous skin cancer, noninvasive breast cancer (DCIS), or prostate cancer under active surveillance). Other malignancies are allowed if patient has been disease free for a minimum of three years
3. Prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields.
4. Any major surgery within 28 days prior to study entry, except colonic stent placement, intestinal diversion without resection or vascular access insertion.
5. Severe, active comorbidity, defined as follows:

   1. Unstable angina and/or congestive heart failure requiring hospitalization within the last six months.
   2. Transmural myocardial infarction within three months prior to study entry.
   3. Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration.
   4. Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration.
   5. Uncontrolled malabsorption syndrome significantly affecting gastrointestinal function.
   6. Any unresolved intestinal obstruction.
   7. Acquired immune deficiency syndrome (AIDS), based upon current Centers for Disease Control and Prevention (CDC) definition. Note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because patients receiving antiretroviral therapy may experience possible pharmacokinetic interactions with required treatment medications, such as capecitabine.
   8. Absence of any significant medical comorbidity which would preclude the consideration of major intestinal surgery.
6. Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception during the course of the study and for women three months after study therapy is completed and for men six months after study therapy is completed. This exclusion is necessary because the treatment involved in this study may be significantly teratogenic.
7. Participation in another interventional clinical treatment trial while on study (observational trials are permitted).
8. Patients taking nonprotocol-specified chemotherapy agents or immune-modulating agents for other medical conditions are not permitted to participate in this trial. Any medication questions should be reviewed by the PI.
9. Poor functional status such that patients are not able to be positioned for radiation treatments.
10. Gadolium allergy.
11. If age over 60, history of hypertension, diabetes or liver transplant, and glomerular filtration rate (GFR) at enrollment is \< 30.

Where this trial is running

Milwaukee, Wisconsin

• Froedtert & the Medical College of Wisconsin — Milwaukee, Wisconsin, United States (Recruiting)

Study contacts

• Principal investigator: William Hall, MD — Medical College of Wisconsin
• Study coordinator: Medical College of Wisconsin Cancer Center Clinical Trials Office

Conditions Rectal Adenocarcinoma; MR-guided radiation therapy; Rectal adenocarcinoma