Treatment of Radiation and Cisplatin Induced Toxicities With Tempol
A 10 week trial to assess the ability of Tempol to prevent and/or reduce toxicities associated with cisplatin and radiation treatment in head and neck cancer patients. Over the course of the 10 week trial, mucositis, nephrotoxicity, and ototoxicity will be monitored and assessed.
A Double Blind, Placebo Controlled Dose Range Finding Study to Assess the Safety, Pharmacokinetics, and Efficacy of Tempol for the Reduction of Severe Mucositis in Head and Neck Cancer Patients Undergoing Combined Radio- and Chemotherapy
One hundred and twenty (120) participants with head and neck cancer are scheduled to undergo combined radio- and chemotherapy (n = 120).
Nearly all (90% to 97%) participants receiving radiotherapy in the head and neck will develop some degree of mucositis. Of these participants treated with radiotherapy with or without chemotherapy, 34% to 43% will present severe mucositis. As a result, the participant's quality of life is affected, hospital admittance rates are higher, the use of total parenteral nutrition is increased and interruption of treatment is more frequent, all of which compromise tumor control. Mucositis causes 9% to 19% of chemotherapy and radiotherapy interruption.
A common chemotherapeutic agent used in head and neck cancer is Cisplatin. Cisplatin (cis- diamminedichloroplatinum(II), CDDP) is an antineoplastic drug used in the treatment of many cancers including testicular cancer, ovarian cancer, bladder cancer, head and neck cancer, esophageal cancer, small and non-small cell lung cancer, breast cancer, cervical cancer, stomach cancer, prostate cancer, brain tumors, neuroblastoma, sarcomas, multiple myeloma, melanoma, mesothelioma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, pancreatic cancer, and thyroid cancer. While toxicities include ototoxicity, gastrotoxicity, myelosuppression, and allergic reactions, the main dose-limiting side effect of cisplatin is nephrotoxicity followed by ototoxicity.
Tempol is a piperidine nitroxide. Nitroxides are a class of stable free radical compounds that have anti-oxidant activity protecting mammalian cells against numerous toxic agents including hydrogen peroxide, superoxide, and t-butyl hydroperoxide cytotoxicity. This anti-oxidant activity of Tempol has led to its investigation as a potential radioprotector and chemoprotectant. In radiation and chemotherapy, Tempol protects normal cells from radiation and cisplatin-induced damage; however, in cancerous or tumor cells, Tempol is reduced to its hydroxylamine form that does not and cannot protect the cells from radiation and cisplatin induced damage. This distinction is of particular importance in the setting of cancer treatment, in which both normal and tumor tissue is exposed to radiation and chemotherapy. Without using Tempol, both normal cells and cancer cells suffer from toxicity. Tempol is the only known compound to possess this functional duality. Because of Tempol's free-radical scavenging ability, this compound is able to prevent many of the toxicities associated with cisplatin and radiation treatment including the prevention of mucositis, nephrotoxicity, and ototoxicity.
The first group 60 participants will be randomized 1:1 to either Tempol 600 mg daily or placebo. Assuming that treatment is well tolerated but ≥20% of the participants in the active arm have grade 3 or 4 mucositis, a second group of 60 participants may be enrolled, and randomized 1:1 to receive either Tempol 1000 mg daily or placebo.
Throughout the treatment period, participants will take study medication twice daily on both chemo/radiation days and cancer treatment free days. On radiation/chemo days, participants will be instructed to take study medication 10 minutes before each proton therapy or radiation treatment (400 or 600 mg) and again in the evening (200 or 400 mg) no less than 6 hours following the first dose. Participants will begin to take study medication two (2) days before their scheduled cancer treatment. When proton therapy or radiation is not administered, participants will take the medication twice daily, 400 mg or 600 mg in the morning and 200 mg or 400 mg in the evening. On the day of radiation therapy, study medication will be administered within 10 minutes prior to each course of radiotherapy. Participants will be instructed to hold the solution in their mouth swishing for approximately 30 seconds and then swallow.
Mucositis Nephrotoxicity Ototoxicity cisplatin toxicity Pharmaceutical Solutions Cisplatin Tempol TEMPO
You can join if…
Open to people ages 18 years and up
- Be ≥18 years of age with medically diagnosed squamous cell cancer of the head and neck (SCCHN);
- Be scheduled to receive definitive radiotherapy or proton therapy administered with a curative intent;
- If female and of child bearing potential, be using an effective birth-control method with a history of reliability for the individual participant;
- If male and of child bearing potential, adequate methods of contraception must be employed including use of condoms with spermicide. No sperm donation for 90 days until after the conclusion of the study;
- Must be receiving cisplatin for chemotherapy;
- Be properly informed of the nature and risks of the clinical investigation, comply with all clinical investigation-related procedures, and sign an Informed Consent Form prior to entering the clinical investigation;
- Must have a score 2 or less on the Eastern Cooperative Oncology Group (ECOG) performance status;
- Participant life expectancy ≥ 6 months; and
- Adequate baseline organ function (hematologic, liver, renal, nutritional and metabolic):
Absolute neutrophil count (ANC) ≥1.5 Hemoglobin ≥ 10 g/dL Platelets ≥ 100,000 per microliter of blood
Total bilirubin ≤ 2 X (Upper limit normal) ULN Alanine amino transferase (ALT) and Aspartate aminotransferase (AST) ≤5 x ULN
Serum creatinine ≤ ULN or, if > ULN calculated creatinine clearance (CrCl) ≥ 60 mL/min.
Nutritional and metabolic:
Urine Albumin > 3.0 mg/dl
You CAN'T join if...
- Prior radiotherapy of the head and neck;
- Have a clinically significant infection defined as any acute viral, bacterial or fungal infection, which requires specific therapy. Anti-infectious therapy must have been completed within 14 days of starting study treatment;
- Be taking any non-approved therapy for oral mucositis, including β-carotene, tocopherol, laser irradiation, brushing the oral mucosa with silver-nitrate prophylactically, systemic TGF-β (transforming growth factor beta), or systemic KGF (keratinocyte growth factor) during or within 14 days of starting treatment;
- Be taking mugard;
- Be taking prostaglandins, pentoxifylline or leucovorin during or within 14 days of starting treatment;
- Be rinsing with allopurinol, hydrogen peroxide, sucralfate, or chlorhexidine mouthwashes during or within 14 days of starting treatment;
- Have had a recent, serious, non-malignant medical complication that, in the opinion of the investigator, makes the individual unsuitable for study participation;
- Have used an investigational drug within 28 days of the initiation of study treatment;
- Have a history of a positive blood test for HIV;
- . At the time of screening, having a significant active medical illness which, in the opinion of the investigator, would preclude completion of the study;
- . Participants with a treatment plan consisting of chemoradiation followed by further chemotherapy;
- . Participants with body weight less than 35 kg, 77 lbs;
- . Women who are pregnant or who are breastfeeding;
- . Participants with known hearing loss;
- . Participants with known intolerance to platin drugs;
- . History of insulin-dependent Diabetes Mellitus; and
- . Participants with Hepatitis B/C.
accepting new patients
La Jolla California 92093 United States
- The University of Kansas Cancer Center
not yet accepting patients
Westwood Kansas 66205 United States
Lead Scientist at UCSD
- James Urbanic, MD
Associate Professor Of Clinical, Radiation Medicine and Applied Science. Authored (or co-authored) 52 research publications
- accepting new patients
- Start Date
- Completion Date
- Matrix Biomed, Inc.
- Phase 2
- Study Type
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study. Submitting your contact information does not obligate you to participate in research.
The study team should get back to you in a few business days.