PET/MRI in Rectal Cancer

Rectal Cancer Clinical Trial

Official title:

18FDG-PET/MRI Imaging in Predicting Pathological Response to Total Neo-adjuvant Therapy in Rectal Cancer

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06057831
• Other study ID #: IIT-0034
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: December 2024
• Est. completion date: December 2024

Study information

• Verified date: June 2024
• Source: AHS Cancer Control Alberta
• Contact: Kurian Joseph
• Phone: 780-432-8755
• Email: kurian.joseph[@]ahs.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to see which participants have a better treatment response using PET/MRI imaging to study the removed tumor, after they have received a total neoadjuvant therapy (TNT). The treatment choice of long course chemo-radiotherapy treatment will be determined by institutional policy.

The researchers will also be looking at whether this study could significantly improve the future management and quality of life of rectal cancer patients.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 40
• Est. completion date: December 2024
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients with histologically proven adenocarcinoma of the rectum.

2. Clinical stage 2-3 rectal adenocarcinoma, cT3/4N0/M0 or Tx N1-2/M0, within 16 cm from anal verge (lesion below the sacral promontory).

3. Patients deemed suitable to undergo TNT followed by surgical resection.

4. Male or female = 18 years of age.

5. ECOG/Zubrod status 0-2.

6. Able and willing to follow instructions and comply with the protocol.

7. Provide written informed consent prior to participation in the study.

8. Women of childbearing potential (WOCBP) must have a negative serum (or urine) pregnancy test at the time of screening if there is concern about pregnancy. WOCBP is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy or bilateral oophorectomy or bilateral salpingectomy) and is not postmenopausal.

9. If female of child-bearing potential and outside of the window of 10 days since the first day of the last menstrual period, concerned about pregnancy are not eligible for the study.

10. Females must not be breastfeeding (during treatment and at least 6 months from the last dose).

11. Male patients should agree that not donate sperm during the study (during treatment and at least 6 months from the last dose).

12. Patients of childbearing/reproductive potential should use highly effective birth control methods if indicated, as defined by the investigator, up to the period of finishing adjuvant chemotherapy. A highly effective method of birth control is defined as those that result in low failure rate (i.e., less than 1% per year) when used consistently and correctly.

Note: abstinence is acceptable if this is established and preferred contraception for the patient and is accepted as a local standard.

Exclusion Criteria:

1. Patient receiving short course radiotherapy alone for rectal cancer.

2. Patient receiving standard TNT.

3. Patients with metastatic disease.

4. Prior pelvic radiotherapy or chemotherapy.

5. Patients in whom MRI is contra-indicated as per prevailing institutional guidelines (e.g. pacemakers, aneurysm clips, cochlear implant, implanted cardiac defibrillator).

6. Prior or concurrent malignancy (except non-melanomatous skin cancer) unless disease-free for at least 5 years.

7. Inability to lay in supine position for approximately one hour.

8. Nursing or pregnant females.

9. Age <18 years.

10. Previous and concurrent, experimental, chemotherapy, or radiotherapy treatment for primary rectal carcinoma.

11. Patients with malabsorption syndrome, ulcerative colitis, inflammatory bowel disease, resection of the stomach or small bowel, or other disease significantly affecting gastrointestinal (GI) function.

12. Patients with a known history of documented upper GI bleeding or upper GI ulcerative disease.

13. Patients who have experienced untreated and/or uncontrolled cardiovascular conditions and/or have symptomatic cardiac dysfunction.

14. Known current alcohol abuse.

15. Patients with symptomatic inflammatory bowel disease.

16. Patients with uncontrolled hypothyroidism.

17. Patients with chronic liver disease.

18. Patients known to be suffering from infection with HIV, Tuberculosis, Hepatitis C or Hepatitis B.

19. Any contra-indications for intravenous contrast.

20. History of anaphylactic reaction to medications or drug allergy.

Related Conditions & MeSH terms

• Rectal Cancer
• Rectal Neoplasms

Intervention

Radiation:
• Total Neo-adjuvant Therapy
TNT incorporates chemotherapy with concurrent chemoradiotherapy (CRT) in any order. Radiotherapy includes 5000 cGy/25 fractions over 5 weeks. Chemotherapy regimen for Concurrent CRT: Capecitabine Chemotherapy regimens used with TNT are: FOLFIRINOX x 6 cycles, 8-9 courses FOLFOX or 5-6 courses of CAPEOX delivered over 4-6 months. The chemotherapy regimen or the order of treatment will be decided at the discretion of the patient's medical oncologist

Other:
• 18FDG-PET/MRI scan
18FDG-PET/MRI scan within 4 weeks of commencing chemo-radiation and within 1 - 2 weeks before radical rectal cancer surgery.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
AHS Cancer Control Alberta

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint of the study is pathological response (pCR) prediction with PET/MRI.	A 3-point scale will be used on PET/MRI assessment. When PET and MRI are concordant, the score remains unchanged. When MRI or PET are discordant, but one modality is definitive for complete response (e.g., MRI showing low intensity crescent at site of tumor or no uptake is identified on corresponding location on PET), a tumor regression grade (TRG) score of 1 will be assigned.	Week 29 - Week 31
Primary	Correlation between PET/MRI reported pCR and complete(pCR) or incomplete response(non-pCR) to total neoadjuvant therapy determined by final pathology will be defined.	The pathologic response to the total neo-adjuvant therapy will be assessed generally using classification of tumor regression grade (TRG) defined by Mandard et al.	Week 31
Secondary	To evaluate the significance of PET/MRI compared to MRI to predict response to TNT.	MRI imaging performed before and after TNT and the post TNT scans will be compared to baseline to identify the degree of regression. This comparison to baseline imaging will be performed to avoid misinterpretation of pseudotumor (inflammatory changes within normal rectal wall adjacent to regressed tumor) as residual tumor.	Week 29 - Week 31 (1 - 2 weeks before surgery)
Secondary	A feasibility study done to evaluate the benefit of using PET/MRI with respect to improved identification of the target and hence target delineation	Therapy plans are generated using image measures derived from standard radiotherapy plans or PET/MRI imaging. CT imaging is the standard imaging procedure used for radiotherapy treatment planning. In this clinical trial, a therapy plan will be generated from the initial PET/MRI imaging performed in the radiotherapy treatment position. This therapy plan will be compared with standard radiotherapy plans to evaluate the significance of using PET/MRI in radiotherapy treatment planning.	Week 29 - Week 31 (1 - 2 weeks before surgery)