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clinical trials |
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Aim 3: Develop and Test Approaches for Controlling Cancer-Related Symptoms and Cancer Treatment-Related Side EffectsThe symptom control efforts of the Mayo CPC Program have been organized into sub-areas of concentration. The various efforts within Mayo's Symptom Control Program are led by the following individuals under the guidance of Charles Loprinzi, M.D., who also leads hot flash research and treatment-induced neuropathy research:
Treatment-Induced Mucosal and Epidermal Injury The National Cancer Institute (NCI) has approved another protocol developed by Dr. Jatoi as a follow-up trial in this area which, in another double-blind, placebo-controlled Phase III manner, evaluated the potential benefit of a sunscreen as a means of preventing the EGFR-associated rash (N05C4). This study completed its planned accrual and is being analyzed. Dr. Jatoi hast other similar research initiatives under development. In 2007, Dr. Martenson led an effort to study mometasone furoate versus a placebo for the prevention of radiation dermatitis in patients receiving radiation therapy (N06C4), which opened in the summer of 2007 and accrued over 150 patients within four months. Preliminary results from this trial demonstrate that it decreases radiation therapy-induced dermatitis. Treatment of Cancer Anorexia/Cachexia Ongoing evaluations in this area include the analysis and reporting of three clinical trials. One trial, led by Dr. Jatoi and Michele Halyard, M.D., examined zinc replacement in patients receiving radiation therapy to the head and neck to try to prevent troubles with dysgeusia (N01C4). This trial met its accrual goal in 2005 and was published in 2007. Two other trials, led by Dr. Jatoi, addressed inhibitors of tumor necrosis factor. One of these evaluated infliximab in patients with non-small cell lung cancer (N01C9). Another of these trials evaluated etanercept (NOOC1) in patients with anorexia/cachexia. These two trials have been closed for accrual; one is still undergoing analysis while the other has been published. Another trial led by Dr. Jatoi, evaluating creatine for patients with cancer anorexia/cachexia (N02C4) recently reached its accrual goal of 300 patients. In addition, she recently obtained R01 funding to conduct a trial looking at the purported value of wine in patients with anorexia/cachexia. Hot Flashes A Phase III trial of citalopram for the treatment of hot flashes (N05C9) opened for accrual in the fall of 2006 and completed the accrual of 220 patients by April 2007. Dr. Barton, the primary investigator of this trial, collaborated with pharmacogenomics experts at Mayo Clinic, in particular, Matthew Goetz, M.D., and Matthew Ames, Ph.D. (Developmental Therapeutics Program). A translational research study was included as a part of this citalopram study, to determine whether CYP2D6 and CYP2C19 genetic alterations could predict hot flash frequency, severity and dosing needs. Samples from patients are now undergoing analyses. In an additional trial, Dr. Sood is actively conducting a 3-arm randomized pilot trial, looking at paced breathing as a means of decreasing hot flashes. Another trial was recently opened by Dr. Loprinzi to evaluate pregabalin in women with hot flashes. The data supporting this protocol are based on the positive experience that has been demonstrated with gabapentin as an agent to treat hot flashes. CPC researchers continue to evaluate potential agents to treat hot flashes in both men and women, seeking to develop new options for patients. Osteoporosis A new study will be beginning soon, assessing whether a new monoclonal antibody targeting the RANK ligand, denosumab, will be effective at attenuating chemotherapy-associated bone loss in premenopausal women receiving adjuvant cytotoxic therapy (N06C9). Sexual Health Chemotherapy-Induced Peripheral Neuropathy In addition to treating established chemotherapy-induced neuropathy, we have developed protocols to try to prevent it. A Phase III placebo-controlled protocol, coordinated by Dr. Grothey sought to evaluate a calcium and magnesium preparation in an effort to try to prevent oxaliplatin-induced neuropathy (N04C7). Positive results from this trial have been accepted for an oral presentation at the 2008 annual ASCO meeting. Another Phase III placebo-controlled study, evaluating vitamin E as an agent to prevent chemotherapy induced neuropathy and led by Lisa Kottschade, rapidly completed its accrual goal and is undergoing analysis. These latter two studies have translational components that will evaluate genetic determinants that might indicate patients at risk for neuropathy. These translational efforts have involved Dr. Goetz and Richard Weinshilboum, M.D. Treatment of Cytopenias Alleviation of Fatigue Cognition and Mood Pain Control This pilot experience has led to another trial whereby this cryoablation procedure is being compared, in a randomized manner, to standard external beam radiation therapy as a primary treatment for painful bony metastases (N06C6).
Traditional Pharmacotherapy Dr. Hurt is a co-investigator on a multicenter grant testing methylphenidate for treating tobacco dependence in smokers with ADHD and he recently was awarded an R21 to test the efficacy of methyplphenidate for treating tobacco dependence in smokers. Amit Sood, M.D., conducted an intramurally-funded pilot study which led to a trial using gabapentin for treating tobacco dependence. Dr. Sood, in collaboration with Dr. Ebbert, has also initiated a pilot trial using varenicline and sibutramine to treat smokers with the aim of testing whether the combination will help smokers to stop smoking without gaining weight. Nicotine researchers have collaborations with colleagues in the Department of Laboratory Medicine seeking to develop capabilities of assaying biological fluids for tobacco alkaloids. Recently Thomas Moyer, Ph.D., developed, tested, and instituted for research and clinical purposes the ability to measure nicotine, cotinine, trans-3-hydroxycotinine, anabasine, and nornicotine, utilizing HPLC-tandem mass spectrometry methodology. This allows researchers to measure these tobacco alkaloids at a level of precision not previously available at Mayo Clinic. This capability has resulted in better clinical practice, especially in the Mayo Clinic Transplant Program. In order to go onto the heart transplant list, the patient must be abstinent from tobacco for a minimum of six months. If the patient is a tobacco user, treatment in our Residential Treatment Program is mandated by the transplant team. The transplant team utilizes the highly specific tobacco alkaloid assays from Dr. Moyer's laboratory to biochemically confirm the patient's abstinence from tobacco and also to distinguish between tobacco use and nicotine replacement therapy.
Complementary and Alternative Medicine Approaches
Alcoholic Smokers
Smokeless Tobacco With funding through the Cancer Center from the Fraternal Order of Eagles, Drs. Ebbert, Dale, Hurt and Ivana Croghan, Ph.D., conducted an open label pilot study treating smokeless tobacco users using the 4 milligram (mg) nicotine lozenge. Biochemically-confirmed 7-day point prevalence tobacco abstinence 12 weeks (end-of-treatment) was 53 percent and 47 percent at six months, which led to the submission and funding of a new grant and continued study. In the new clinical trial, Drs. Ebbert, I. Croghan, and Hurt are investigating the efficacy of the nicotine lozenge for smokeless tobacco users. They are collaborating as well with Herbert Severson, Ph.D., at the Oregon Research Institute in Eugene, Ore. Dr. Ebbert has also competed successfully for funding from the Fraternal Order of Eagles for an open label trial using varenicline and bupropion for smokeless tobacco users. His ongoing collaborative relationship with Dorothy Hatsukami, Ph.D., at the University of Minnesota has now developed to the point that the University will be a site for the varenicline/bupropion grant submission in June 2008. In a related pilot project Paul Limburg, M.D., in collaboration with Drs. Hurt and I. Croghan developed and pilot tested a scannable questionnaire to survey patients who come for gastrointestinal endoscopy at Mayo Clinic in Rochester, Minn., to assess their tobacco use history. It is known that cigarette smoking has been associated with increased risk for esophageal squamous cell carcinoma, esophageal adenocarcinoma, and colorectal adenocarcinomas, but observational data regarding the use of smokeless tobacco and gastrointestinal cancer risk have not been rigorously examined. Since smokeless tobacco contains many of the same carcinogens found in cigarettes and since smokeless tobacco users frequently swallow their tobacco juice, this likely would increase the topical gastrointestinal exposure to carcinogens and may increase the risk of malignant transformation at one or more sites within this organ system. Dr. Limburg has surveyed over 3,000 patients and data analysis is in progress. If a relationship is shown, this will open up an avenue of research, not only for interventions for smokeless tobacco users but also to establish the feasibility of collecting cancer risk factor data from a large patient population with the documented presence or absence of gastrointestinal mucosal lesions, develop data collection instruments (in scannable format) that may be applied to observational studies of multiple gastrointestinal cancers, and to construct the foundation for a data resource that will facilitate future large-scale epidemiologic investigations of gastrointestinal cancer risk and protective factors. Treating tobacco dependence in cancer patients and outcome evaluations of patients treated at the NDC Treatment Program Very little work has been performed in treating tobacco dependence in patients with cancer, but Mayo investigators continue to try to close the research gap. Yolanda Garces, M.D., in the Department of Radiation Oncology has a number of ongoing projects treating tobacco dependence in Radiation Oncology patients. Along with Dr. Hurt and Gary Croghan, M.D., Ph.D., her research fills a major void in available knowledge. Her research shows that head and neck cancer patients who have been treated in the Nicotine Dependence Center Treatment Program who continue to smoke are much more likely to develop a second primary cancer, and this happens within a very short period of time (i.e., 1 to 3 years). Dr. Garces is continuing this work through an intramurally-funded CR20 grant "Tobacco Use in Radiation Oncology Patients." Dr. Ames has also continued to help evaluate the NDC's clinical program by performing an analysis of different variables in the Residential Treatment Program and found that there was improvement across a range of psychosocial factors. Finally, Dr. I. Croghan and Sandhya Pruthi, M.D., (Women's Cancer Program) have utilized intramural funding and existing databases to evaluate the potential relationship between smoking and breast cancer or other breast diseases and to evaluate the NDC Treatment Program outcomes to determine if there are differences based on gender. Dr. I. Croghan along with Dr. Hurt and Charles Loprinzi, M.D., published the results of the third North Central Cancer Treatment Group (NCCTG) trial of treatments for smokers in a randomized comparison of a nicotine inhaler and bupropion and reported that the nicotine inhaler significantly increased smoking abstinence beyond the effect of bupropion alone.
Young Adult Smokers and Surgical Patients
Ethnic and Racial Differences
Surgical Patients
Tobacco Document Research
Genetic Epidemiology and Risk Assessment Program
Minnesota Tobacco Control Research and Policy Center Specifically, this center will:
The Center will establish linkages throughout relevant dimensions of the University and Mayo communities - from basic biology to international prevention and treatment - but will reach significantly further, for example, to include treatment service providers such as Blue Cross Blue Shield Minnesota and valuable industrial partners engaged in the development of medications and biomedical instrumentation. By developing infrastructure supported by intramural resources, the investigators will efficiently integrate the existing tobacco control efforts which are wide ranging but diffusely located into an overarching framework which in turn will support cohesive approaches to facilitate the acquisition of extramural funding to support ongoing research, training, and clinical practice objectives. |
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