Papaverine in Combination With Radiation Therapy for the Treatment of Locally Advanced Rectal Cancer, DINOMITE Trial
July 21, 2026 updated by: City of Hope Medical Center
DINOMITE (Decreasing Hypoxia With Mitochondrial Inhibition in Locally Advanced Rectal Cancer): Phase 1 Trial of Papaverine in Combination With Radiation
This phase I trial studies the side effects and best dose of papaverine (PPV) when given together with radiation therapy (RT) and tests how well it works in treating patients with rectal cancer that has spread to nearby tissue or lymph nodes (locally advanced).
PPV is an enzyme inhibitor, and it may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
RT uses high energy x-rays, particles, or radioactive seeds to kill tumor cells and shrink tumors.
Giving PPV with RT may be safe, tolerable, and/or effective in treating patients with locally advanced rectal cancer.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
- Procedure: Magnetic Resonance Imaging
- Radiation: Radiation Therapy
- Procedure: Computed Tomography
- Procedure: Functional Magnetic Resonance Imaging
- Procedure: Biospecimen Collection
- Drug: Consolidation Therapy
- Procedure: Gastrointestinal Endoscopy
- Procedure: Total Mesorectal Excision
- Drug: Papaverine
Detailed Description
PRIMARY OBJECTIVES:
I. Determine the maximum tolerated dose (MTD) and the recommended phase II dose (RP2D) of papaverine (PPV) in combination with radiation therapy (RT) for locally advanced rectal cancer (LARC).
II. Describe the safety and tolerability of PPV in combination with standard of care (SOC) RT for LARC.
SECONDARY OBJECTIVES:
I. Determine the clinical complete response rate (cCR), and local-regional control rate of PPV in combination with RT for LARC.
II. Determine the total mesorectal excision (ToME)-free survival, local-regional recurrence free survival (LRRFS), disease-free survival (DFS), distant-metastasis-free survival (DMFS) and overall survival (OS) of PPV in combination with RT for LARC.
EXPLORATORY OBJECTIVES:
I. Determine whether PPV in combination with RT for LARC directly results in reduced tumor hypoxia.
II. Explore whether RT with and without mitochondrial oxygen consumption (MOC) inhibition alters the tumor immune microenvironment (TIME) in patients receiving SOC RT for LARC.
III. Explore whether molecular profiling (changes in hypoxia-induced gene expression, immune cell tumor infiltrates and peripheral immune profiling) can predict which patients may respond best to PPV in combination with SOC RT for LARC.
IV. Explore whether stool microbial signatures are associated with response to or progression after PPV in combination with SOC RT for LARC.
OUTLINE: This is a dose escalation study of PPV in combination with RT followed by a dose-expansion study. Patients are randomized to 1 of 2 cohorts.
COHORT 1: Patients undergo RT once daily (QD) on days 1-5 (Monday-Friday) of week 1. Starting at week 5, patients receive SOC consolidation chemotherapy (CC) with either modified leucovorin, fluorouracil, oxaliplatin-6 (mFOLFOX6) or capecitabine-oxaliplatin (CAPOX) for 3-4 months in the absence of disease progression or unacceptable toxicity. As early as four weeks following completion of CC, patients with persistent disease (non-cCR) or disease recurrence in the rectum during disease evaluation may undergo ToME. Additionally, patients undergo one functional magnetic resonance imaging (fMRI) on study as well as computed tomography (CT), magnetic resonance imaging (MRI), endoscopy, and blood and tissue sample collection throughout the trial.
COHORT 2: Patients receive PPV intravenously (IV) over 15-30 minutes on day -3 of week 0 and days 1-5 of week 1. Patients also undergo RT QD on days 1-5 (Monday-Friday) of week 1, 1-2 hours after PPV. Starting at week 5, patients receive SOC CC with either mFOLFOX6 or CAPOX for 3-4 months in the absence of disease progression or unacceptable toxicity. As early as four weeks following completion of CC, patients with persistent disease (non-cCR) or disease recurrence in the rectum during disease evaluation may undergo ToME. Additionally, patients undergo two fMRI on study as well as CT, MRI, endoscopy, and blood and tissue sample collection throughout the trial.
After completion of study treatment, patients are followed up every 3 months for 2 years and then every 6 months for an additional 3 years.
Study Type
Interventional
Enrollment (Estimated)
36
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Duarte, California, United States, 91010
- Recruiting
- City of Hope Medical Center
-
Principal Investigator:
- Terence M. Williams
-
Contact:
- Terence M. Williams
- Phone Number: 626-218-2332
- Email: terwilliams@coh.org
-
-
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.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Documented informed consent of the participant and/or legally authorized representative
- Willingness to participate in all correlative studies: fMRI, and tissue collection of tumor and normal rectum (ribonucleic acid [RNA]/deoxyribonucleic acid [DNA]/protein), blood (plasma/peripheral blood mononuclear cell [PBMC]) draws and stool collection
- Age: ≥ 18 years
- Eastern Cooperative Oncology Group (ECOG) ≤ 2
- Histologically confirmed rectal adenocarcinoma
- Patient wants to pursue an organ preservation/non-operative management (NOM) approach after completion of total neoadjuvant therapy (TNT)
- Locally advanced rectal cancer (T3-4 or node+, M0)
- Tumor is microsatellite stable (MSS) (defined as not microsatellite instability-high [MSI-H] or mismatch repair deficient [dMMR])
- Absolute neutrophil count (ANC) ≥ 1,500/mm^3 (within 30 days of start). NOTE: Growth factor is not permitted within 14 days of ANC assessment unless cytopenia is secondary to disease involvement
- Platelets ≥ 100,000/mm^3 (within 30 days of start). NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
- Hemoglobin ≥ 9g/dL (within 30 days of start). NOTE: Red blood cell transfusions are not permitted within 14 days of hemoglobin assessment unless cytopenia is secondary to disease involvement
- Total bilirubin ≤ 1.5 X upper limit of normal (ULN) (within 30 days of start)
- Aspartate aminotransferase (AST) =< 2.5 x ULN (within 30 days of start)
- Alanine aminotransferase (ALT) =< 2.5 x ULN (within 30 days of start)
- Creatinine clearance of ≥ 50 mL/min per 24 hour urine test or the Cockcroft-Gault formula (within 30 days of start)
- For patients with known infections only: seropositive for HIV, hepatitis C virus (HCV) or hepatitis B virus (HBV), nucleic acid quantitation must be performed. Viral load must be undetectable. HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial (within 28 days of start)
- Women of childbearing potential (WOCBP): negative urine or serum pregnancy test. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required (within 30 days of start)
Agreement by females and males of childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 4 months after the last dose of protocol therapy
- Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only)
Exclusion Criteria:
- Chemotherapy, biological therapy, immunotherapy within 14 days or five half-lives (whichever is shorter) prior to day 1 of protocol therapy
- Prior pelvic irradiation resulting in overlapping fields
- Use of levodopa in the last 30 days
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent
- Unable to undergo MRI and endoscopic procedures
- History of complete atrioventricular block, hepatic dysfunction (e.g. cirrhosis), or priapism
- Other active malignancy. Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
- Females only: Pregnant or breastfeeding
- Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
- Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Cohort 1 (RT, CC)
Patients undergo RT QD on days 1-5 (Monday-Friday) of week 1.
Starting at week 5, patients receive SOC CC with either mFOLFOX6 or CAPOX for 3-4 months in the absence of disease progression or unacceptable toxicity.
As early as four weeks following completion of CC, patients with persistent disease (non-cCR) or disease recurrence in the rectum during disease evaluation may undergo ToME.
Additionally, patients undergo one fMRI on study as well as CT, MRI, endoscopy, and blood and tissue sample collection throughout the trial.
|
Undergo MRI
Other Names:
Undergo RT
Other Names:
Undergo CT
Other Names:
Undergo fMRI
Other Names:
Undergo blood and tissue sample collection
Other Names:
Receive CC with mFOLFOX6 or CAPOX
Other Names:
Undergo endoscopy
Other Names:
Undergo ToME
Other Names:
|
|
Experimental: Cohort 2 (PPV, RT, CC)
Patients receive PPV IV over 15-30 minutes on day -3 of week 0 and days 1-5 of week 1.
Patients also undergo RT QD on days 1-5 (Monday-Friday) of week 1, 1-2 hours after PPV.
Starting at week 5, patients receive SOC CC with either mFOLFOX6 or CAPOX for 3-4 months in the absence of disease progression or unacceptable toxicity.
As early as four weeks following completion of CC, patients with persistent disease (non-cCR) or disease recurrence in the rectum during disease evaluation may undergo ToME.
Additionally, patients undergo two fMRI on study as well as CT, MRI, endoscopy, and blood and tissue sample collection throughout the trial.
|
Undergo MRI
Other Names:
Undergo RT
Other Names:
Undergo CT
Other Names:
Undergo fMRI
Other Names:
Undergo blood and tissue sample collection
Other Names:
Receive CC with mFOLFOX6 or CAPOX
Other Names:
Undergo endoscopy
Other Names:
Undergo ToME
Other Names:
Given IV
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acute dose limiting toxicity (DLT)
Time Frame: From time of single-agent papaverine (PPV) week 0 treatment to start of consolidation chemotherapy (CC), assessed up to 4 weeks
|
As assessed by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5.0.
A defined adverse event considered to be possibly, probably, or definitely related to study treatment (radiation therapy or PPV).
Will employ the time-to-event Bayesian optimal interval design (TITE-BOIN) to find the maximum tolerated dose (MTD).
|
From time of single-agent papaverine (PPV) week 0 treatment to start of consolidation chemotherapy (CC), assessed up to 4 weeks
|
|
Late DLT
Time Frame: From the start of CC week 5 treatment to 12 months from week 0
|
As assessed by NCI CTCAE v5.0.
A defined adverse event considered to be possibly, probably, or definitely related to study treatment (radiation therapy or PPV).
Will employ the TITE-BOIN design to find the MTD.
|
From the start of CC week 5 treatment to 12 months from week 0
|
|
Incidence of treatment related adverse events during acute DLT period
Time Frame: From time of single-agent PPV week 0 treatment to start of CC, assessed up to 4 weeks
|
As assessed by NCI CTCAE v5.0.
Will be delineated by grade and attribution.
A defined adverse event considered to be possibly, probably, or definitely related to study treatment (radiation therapy or PPV).
|
From time of single-agent PPV week 0 treatment to start of CC, assessed up to 4 weeks
|
|
Incidence of treatment related adverse events during late DLT period
Time Frame: From the start of CC week 5 treatment to 12 months from week 0
|
As assessed by NCI CTCAE v5.0.
Will be delineated by grade and attribution.
A defined adverse event considered to be possibly, probably, or definitely related to study treatment (radiation therapy or PPV).
|
From the start of CC week 5 treatment to 12 months from week 0
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical complete response rate
Time Frame: From time of single agent papaverine (PPV) week 0 treatment to completion of consolidation chemotherapy (CC), assessed up to 20 weeks.
|
Will be defined as percent of evaluable patients having no evidence of disease as assessed by magnetic resonance imaging/endoscopy.
Will be summarized by cohort and dose level.
|
From time of single agent papaverine (PPV) week 0 treatment to completion of consolidation chemotherapy (CC), assessed up to 20 weeks.
|
|
Local-regional control rate
Time Frame: From time of single agent papaverine (PPV) week 0 treatment to completion of consolidation chemotherapy (CC), assessed up to 20 weeks.
|
Will be defined as percent of evaluable patients having no evidence of pelvic recurrence in the areas of the primary tumor and regional lymph nodes.
|
From time of single agent papaverine (PPV) week 0 treatment to completion of consolidation chemotherapy (CC), assessed up to 20 weeks.
|
|
Local-regional recurrence free survival
Time Frame: From enrollment to date of first local regional recurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
From enrollment to date of first local regional recurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
|
|
Total mesorectal excision free survival
Time Frame: From enrollment to date of total mesorectal surgical excision, death as result of any cause or being censored at last contact, assessed up to 5 years
|
From enrollment to date of total mesorectal surgical excision, death as result of any cause or being censored at last contact, assessed up to 5 years
|
|
|
Disease-free survival
Time Frame: From enrollment to date of first disease recurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
From enrollment to date of first disease recurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
|
|
Distant-metastasis-free survival
Time Frame: From enrollment to date of first distant metastases occurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
From enrollment to date of first distant metastases occurrence, death as a result of any cause or being censored at last contact, assessed up to 5 years
|
|
|
Overall survival
Time Frame: From enrollment to date of death as a result of any cause or being censored at last contact, assessed up to 5 years
|
From enrollment to date of death as a result of any cause or being censored at last contact, assessed up to 5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Terence M Williams, City of Hope Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 7, 2025
Primary Completion (Estimated)
September 19, 2028
Study Completion (Estimated)
September 19, 2028
Study Registration Dates
First Submitted
December 27, 2024
First Submitted That Met QC Criteria
February 13, 2025
First Posted (Actual)
February 19, 2025
Study Record Updates
Last Update Posted (Actual)
July 22, 2026
Last Update Submitted That Met QC Criteria
July 21, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neoplasms by Site
- Neoplasms
- Intestinal Diseases
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Digestive System Diseases
- Gastrointestinal Diseases
- Colorectal Neoplasms
- Intestinal Neoplasms
- Rectal Diseases
- Rectal Neoplasms
- Heterocyclic Compounds
- Heterocyclic Compounds, 2-Ring
- Heterocyclic Compounds, Fused-Ring
- Investigative Techniques
- Therapeutics
- Clinical Laboratory Techniques
- Diagnostic Techniques and Procedures
- Diagnosis
- Surgical Procedures, Operative
- Drug Therapy
- Minimally Invasive Surgical Procedures
- Physical Phenomena
- Alkaloids
- Diagnostic Techniques, Surgical
- Endoscopy, Digestive System
- Diagnostic Techniques, Digestive System
- Endoscopy
- Digestive System Surgical Procedures
- Chemistry Techniques, Analytical
- Spectrum Analysis
- Opiate Alkaloids
- Isoquinolines
- Benzylisoquinolines
- Papaverine
- Radiotherapy
- Radiation
- Specimen Handling
- Magnetic Resonance Spectroscopy
- Endoscopy, Gastrointestinal
- Consolidation Chemotherapy
Other Study ID Numbers
- 24405 (Other Identifier: City of Hope Medical Center)
- P30CA033572 (U.S. NIH Grant/Contract)
- NCI-2024-10075 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- R01CA297752 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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