A Study of Neoadjuvant Photodynamic Immunomodulation for Colon Cancer

Sponsor

Edward Nelson (Other)

Overall Status

Withdrawn

CT.gov ID

NCT01522677

Collaborator

University of California, Irvine (Other), National Cancer Institute (NCI) (NIH)

Enrollment

Locations

Arm

Duration (Months)

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The central hypothesis for this study is that it is safe and feasible to administer intraluminal photodynamic therapy (PDT) to colon cancers by colonoscopy to induce localized inflammatory/immune response. The objective is to demonstrate the feasibility and safety of PDT to colon cancer patients administered before surgery and to characterize the inflammatory/immune response at the tumor site and systemically. The long-term objective of these studies is to modify he natural biology of colorectal cancers and improve patient survival.

Condition or Disease	Intervention/Treatment	Phase
Colon Cancer	Drug: PDT with 5-ALA radiosensitization	Phase 1/Phase 2

Detailed Description

The central hypothesis for this study is that it is safe and feasible to administer intraluminal photodynamic therapy (PDT) to colon cancers, via colonoscopy, in the neoadjuvant setting to induce localized tumor cell death and an inflammatory/immune response with an increased Th1 component, utilizing 5-ALA as a photosensitizer. The objective is to conduct an initial phase I/II clinical study to demonstrate the feasibility and safety of colonoscopic, neoadjuvant intraluminal PDT to colon cancer patients administered 96 hours pre-resection, to characterize the inflammatory/immune response at the PDT treated tumor site, and to evaluate the systemic anti-tumor immune response. The long-term objective of these studies is to provide an easily administered, adjunctive, therapeutic maneuver that lacks systemic toxicity, with the potential to modulate the natural biology of colorectal cancers that have not elicited a favorable anti-tumor immune response and to improve patient survival.

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I/II Study of Neoadjuvant Photodynamic Immunomodulation for Colon Cancer

Study Start Date :

Aug 1, 2012

Actual Primary Completion Date :

May 1, 2014

Actual Study Completion Date :

May 1, 2014

Arms and Interventions

Arm	Intervention/Treatment
Experimental: PDT Participants receive neoadjuvant 5-ALA and PDT.	Drug: PDT with 5-ALA radiosensitization Patients receive neoadjuvant PDT with radiosensitizing 5-ALA 4 days prior to surgery for colon cancer. Other Names: Photodynamic therapy 5-ALA

Arm

Intervention/Treatment

Experimental: PDT

Participants receive neoadjuvant 5-ALA and PDT.

Drug: PDT with 5-ALA radiosensitization

Patients receive neoadjuvant PDT with radiosensitizing 5-ALA 4 days prior to surgery for colon cancer.

Other Names:

Photodynamic therapy

5-ALA

Outcome Measures

Primary Outcome Measures

Efficacy [6 months]
Define biologic efficacy of PDT in relation to generation of an immune response at the tumor site and systemically. This will be measured by degree of dendritic cell infiltration into tumor and regional lymph nodes, and degree of systemic immunity directed against colon cancer antigens immediately post procedure and after 6 months.
Safety [6 months]
Safety will be evaluated from enrollment through 6 months. This will be measured by proportion of patients completing planned surgery, proportion of patients experiencing grade 3 or 4 toxicities, and lack of observation of serious adverse events related to the study procedure.

Secondary Outcome Measures

Quality of Life [6 months after completion of participation]
Quality of life will be evaluated 6 months following completion of participation in the study
Sustained immunity [1.5-6 months post completion of participation]
Immunologic parameters will be monitored following completion of the study as a measure of sustained immunity

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Patients must have a histologically proven diagnosis of colorectal cancer.
Have clinical stage I, II, or III disease.
Expected survival must be greater than twelve (12) months.
A Karnofsky Performance Status (KPS) must be 70 or greater (Appendix I).
Patients must be >21 years of age.
No prior therapy.
Female patients must not be lactating and must be surgically sterile (via hysterectomy or bilateral tubal ligation), postmenopausal, or using acceptable methods of contraception if they are of child bearing potential. Female patients of childbearing potential must also have a negative serum pregnancy test.
Patients must be able to understand and sign an informed consent form, which must comply with U.S. regulations (U.S. 21 CFR 50) and ICH guidelines.
Eligible patients must have adequate initial hematologic and coagulation parameters, hemoglobin ≥ 11g/dl, platelet count >50,000, Protime and Prothrombin Time ≤ 1.5 x normal.
Eligible patients must have adequate bone marrow, liver and renal function: ANC > 1500/μL, Platelets >100,000 x μL, total bilirubin < the upper limit of normal (ULN), and creatinine clearance (CrCl) > 45 mL/min

Exclusion Criteria:

Any co-morbidity that precludes primary surgical resection of the colorectal tumor.
Any significant general organ system compromise including:

Liver function, transaminases ≥ 2 x,
Renal function, Cr ≥ 1.5 x upper limit of normal
Pulmonary function, room air O2 saturation <90%
Cardiovascular function, Patients with significant (Class III or IV) cardiovascular disease according to the New York Heart Association's functional criteria (Appendix II)
Gastrointestinal function, i.e. active inflammatory bowel disease or active peptic ulcer disease.

Any contraindication to repeat colonoscopy, such as idiosyncratic reactivity to conscious sedation medications.
Prior treatment for the diagnosis of colorectal cancer, including surgical resection.
Stage IV colorectal cancer, i.e. the clinical presence of metastases
Prior malignant diagnosis except for the basal cell epithelioma of the skin.
Persistent fever greater than 38 C.
Mineral overload syndromes for Lead, Zinc, Copper or Iron.
Use of any agent that modulates 5-ALA metabolism and porphyrin synthesis, e.g. St. John's Wort.
Required use of corticosteroids or immune suppression for any reason including an organ allograft or HIV infection
Patients with any acute or chronic illness including cardiovascular disease (e.g. history of atrial fibrillation or ventricular arrhythmias) or history of myocardial infarction, autoimmune state, or any psychiatric illness that in the opinion of the Investigators would compromise treatment.
Use of investigational drugs within 30 days of execution of the informed consent form.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of California, Irvine	Orange	California	United States	92868
2	Mounst Sinai School of Medicine	New York	New York	United States	10029

Sponsors and Collaborators

Edward Nelson
University of California, Irvine
National Cancer Institute (NCI)

Investigators

Principal Investigator: Randall F Holcombe, MD, Icahn School of Medicine at Mount Sinai
Principal Investigator: Edward L Nelson, MD, University of California, Irvine