Status:
COMPLETED
Phase II Study of Minocycline for Reducing Symptom Burden in Colorectal Patients
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborating Sponsors:
American Cancer Society, Inc.
Conditions:
Colorectal Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The goal of this clinical research study is to learn if minocycline can reduce numbness, pain, and/or loss of motor function in patients with colorectal cancer. In this study, minocycline will be comp...
Detailed Description
Nearly 40% of patients with colorectal cancer who receive oxaliplatin-based chemotherapy experience neuropathy (nerve damage that can include numbness, pain, and/or loss of motor function). Sometimes,...
Eligibility Criteria
Inclusion
- Patients with a pathologically proven diagnosis of CRC seen either at MD Anderson or LBJ.
- Patients \> or = 18 years old.
- Patients who qualify for oxaliplatin-based chemotherapy (in the adjuvant or metastatic setting) and are likely to receive at least 3 months of oxaliplatin.
- Patients who speak English or Spanish (due to language options for the MDASI version being used in this study, we are only recruiting English-speaking or Spanish-speaking patients).
- Patients with an NCI-CTCv4 sensory neuropathy score of 0.
- Patients with adequate renal function (serum creatinine must be \< 1.5 times the upper limit of the institutional normal range) and no prior renal disease that in the opinion of the attending physician would make the patient ineligible to receive the study drug . Test results must be no more than 3 months old.
- Patients with adequate hepatic function (total bilirubin must be \< 2.0 times the upper limit of the institutional normal range; alanine aminotransferase (ALT) and aspartate aminotransferase (AST) must be \< 3.0 times the upper limit of the institutional normal range). Test results must be no more than 3 months old.
- Patients willing and able to review, understand, and provide written consent.
Exclusion
- Patients continuously taking any minocycline within the last 15 days. Patients who have conditions that potentially preclude use of minocycline as determined by the treating physician.
- Patients continuously taking systemic steroids within the last 15 days.
- Patients with autoimmune disorders (for example, systemic lupus erythematosus or rheumatoid arthritis), who have been treated in the last 3 years.
- Patients who are pregnant; the absence of pregnancy will be confirmed by negative urine test.
- Hypersensitivity to any tetracyclines, or a history of other allergies or drug reactions that in the treating physician's judgment make the patient inappropriate for this study.
- Patients receiving vitamin K antagonist (warfarin).
- Patients with a BMI \>40 (Obese Class III criteria).
- Patients who will receive cetuximab or other targeted therapy where physicians may use topical doxycycline to reduce the rash associated with therapy.
Key Trial Info
Start Date :
November 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 14 2019
Estimated Enrollment :
122 Patients enrolled
Trial Details
Trial ID
NCT01906008
Start Date
November 1 2013
End Date
February 14 2019
Last Update
March 17 2020
Active Locations (2)
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1
LBJ Hospital
Houston, Texas, United States, 77030
2
University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030