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Aim 3: Develop and Test Approaches for Controlling Cancer-Related Symptoms and Cancer Treatment-Related Side Effects

The 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
Investigators in the Cancer Prevention Program have a long-established history of evaluating methods for alleviating epidermal and mucosal injury caused by cancer therapy. The expertise we have developed in this area led Dr. Martenson to become a member of the American Society of Clinical Oncology (ASCO) committee looking at guidelines for the treatment of cancer treatment induced diarrhea. This led to a publication regarding these guidelines in the Journal of Clinical Oncology in 2004. Current efforts by Dr. Martenson in this area include the final analysis and development of a manuscript regarding a trial which was designed to study a somatostatin analogue as an agent to prevent diarrhea in patients receiving pelvic irradiation therapy. Unfortunately the therapy did not show any therapeutic benefit.

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
Since 1990, when Mayo Clinic Cancer Center investigators reported the results of the first randomized placebo-controlled trial to demonstrate that a medication (megestrol acetate) could increase appetite and cause non-fluid weight gain in patients suffering from cancer anorexia/cachexia, cancer prevention researchers continue to evaluate agents for alleviating this devastating clinical problem. This line of research has flourished under the leadership of Dr. Jatoi in collaboration with Dr. Loprinzi and others.

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
CPC researchers have published a number of manuscripts regarding clinical trials of various agents for hot flashes. This continues to be an important avenue of research. One trial (N00CB) accrued 220 men with prostate cancer who had hot flashes. This trial, led by Dr. Loprinzi, was a randomized, four-arm, dose-finding clinical trial evaluating gabapentin. The positive results from this trial were accepted for as an oral presentation at the 2007 annual ASCO meeting. A manuscript has been submitted for publication.

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
Recently CPC members have been developing a new area of investigation, relating to another hormone-deprivation consequence, osteoporosis-related issues in patients with cancer. Several studies are in analysis, including one evaluating the utility of low-dose estrogen or a bisphosphonate (risedronate) or both, compared to calcium and vitamin D alone in men receiving androgen ablation for prostate cancer. Another study, evaluating immediate versus delayed use of zoledronic acid for women starting letrozole therapy following tamoxifen (N03CC - jointly led by Drs. Hines and Loprinzi, and Edith Perez, M.D.), accrued 556 patients and demonstrated that upfront zoledronic acid was able to prevent letrozole-associated bone loss. This has been accepted for presentation at the 2008 annual ASCO meeting.

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
In a recent study published by the Behavioral Research Center of the American Cancer Society, change in sexual functioning was the sixth most common problem cited by survivors of various cancers at one year(106). CPC members are pursuing a number of new research directions in this area. Dr. Barton is exploring sexual health in a number of studies evaluate non-hormonal pathways affecting sexual function. Two of the most interesting areas for study development include agents that will affect dopamine, which affects libido and nitric oxide, which is critical for arousal. Another sexual health protocol (N04CA), led by Lisa Kottschade and Dr. Loprinzi, is a placebo-controlled trial to evaluate the utility of two different doses of pilocarpine for alleviating vaginal dryness.

Chemotherapy-Induced Peripheral Neuropathy
Studies to evaluate potential means for alleviating chemotherapy-induced neuropathy, a prevalent problem in clinical practice, are important, as evidenced by very efficient accrual CPC trials have had.

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
In addition to much previous work, Dr. Steensma is currently leading efforts for two clinical trials addressing 1) the utility of intravenous iron in patients receiving darbopoietin (MC04CC), and 2) the utility of darbopoietin versus three different dose/schedules of erythropoietin (RC05CB). Mayo's expertise in this area has recently led to a number of invited editorials for the Journal of Clinical Oncology.

Alleviation of Fatigue
Cancer fatigue is one of the most problematic symptoms for patients with cancer. Dr. Barton conducted pilot trial looking at three different doses of American ginseng in patients suffering from cancer fatigue. This pilot trial provided promising information, supporting the development of a more definitive Phase III trial, again led by Dr. Barton, to be opening soon. Another protocol, currently accruing patients and being led by Dr. Sood, is evaluating Concerta (a long acting methylphenidate preparation) for cancer fatigue (N05C7).

Cognition and Mood
A study evaluating gingko biloba as an agent to try to prevent cognitive dysfunction in patients receiving adjuvant chemotherapy for breast cancer (N00C9), led by Dr. Barton, met its accrual goal of 220 patients. It is currently undergoing analysis. This trial represents one of the first longitudinal studies measuring both subjective and objective chemotherapy out to two years.

Pain Control
Matthew Callstrom, M.D. (Cancer Imaging Program), is the primary investigator on an ongoing single-center prospective clinical trial evaluating an interventional radiology-performed cryoablation procedure. This study has recently been expanded to involve other centers, with a total planned accrual goal of 60 patients. This effort involves treating patients that have one or two painful lesions that cause daily pain at an average of four on a scale of 0 to 10. Percutaneous cryoablation offers at least two important advantages over the use of radiofrequency ablation. First, minimal or no post-ablation pain is observed using cryoablation. In sharp contrast, approximately 70 percent of patients that Mayo has treated with radio frequency ablation required high levels of intravenous analgesia or an epidural catheter for control of pain in the immediate 24-hour period following treatment. Using cryoablation in the treatment of 32 locally-treated patients, no patients have required an epidural catheter for control of post-procedural pain. Second, the ablation margin is accurately visualized using CT imaging during the cryoablation procedure. This allows careful control of the ablation and avoidance of critical structures.

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
Mayo's nicotine research program continues to expand and investigators have led and participated in a number of pharmacological agent studies. A current line of research is utilizing varenicline in a number of venues, including evaluating efficacy for treating smokers with COPD and a new R01 submission by Richard Hurt, M.D., for varenicline treatment for recovering alcoholic smokers. The NDC's widening experience with this medication has led to research in the use of varenicline for smokeless tobacco users with Jon Ebbert, M.D., performing preliminary studies funded through the Cancer Center by the Fraternal Order of Eagles leading to the submission of an R01. Dr. Ebbert has also performed preliminary studies funded through the Cancer Center by the Fraternal Order of Eagles combining varenicline with bupropion to treat tobacco dependence in smokers, which has also led to a new R01 submission.

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
Dr. Sood has ongoing research utilizing a range of complementary and alternative medicine approaches. He began this line of research by surveying patients at the Nicotine Dependence Center regarding their previous use of complementary and alternative medicine approaches to treat their tobacco dependence. Not surprisingly, 27 percent reported prior use but 67 percent reported interest in future use of CAM approaches. His first grant investigated the efficacy of St. John's Wort in treating tobacco dependence. He has recently been awarded a grant to test the efficacy of SAMe for treating smokers. Other ongoing projects include using meditation to prevent relapse to smoking and a very novel project using dark chocolate to treat light smokers.

Alcoholic Smokers
The prevalence of smoking in alcoholics is 2 to 3 times that of the general population. Mayo investigators have had ongoing research in this area for a number of years. Searching for effective treatments for alcoholic smokers led them to capitalize on their considerable experiences with varenicline resulting in a new grant "Efficacy of Varenicline for Recovering Alcoholic Smokers." This research will be conducted in collaboration with the University of Minnesota.

Smokeless Tobacco
Smokeless tobacco use is a major health and addiction problem, particularly for adolescent and young adult males. Long-term use increases the risk of developing a number of oral/periodontal diseases or cancer. Continued smokeless tobacco users reported a high level of nicotine dependence. To address this, Dr. Ebbert, Steven Ames, Ph.D., and Lowell Dale, M.D., determined that barriers to quitting included lack of motivation, nicotine withdrawal symptoms, and stress. These findings have encouraged Dr. Ebbert to continue to refine pharmacologic interventions for smokeless tobacco users and to pursue high-dose nicotine replacement therapy and new pharmacotherapies, such as varenicline. He collaborated with Drs. Hurt, Dale and Moyer; and investigated the use of serum tobacco alkaloids as a biomarker of systemic nicotine exposure in smokeless tobacco users. They determined that serum nicotine was superior to cotinine for this purpose.

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
Dr. Ames conducted a journaling project for young adult smokers and successfully competed for a Florida Department of Health New Investigator Award through the Florida Biomedical Research Program "Stress Management Intervention for Young Cigarette Smokers." This line of research has now resulted in the 2007 submission of an R21, "Refinement of the Adolescent Minor Stress Inventory." He is also primary investigator of an R21 entitled "Smoking Cessation for Young Adults who Binge Drink." In fact, his collaboration with Chudley Werch, Ph.D. at the University of Florida has led to a line of research in tobacco use interventions for young adults ranging from high school age to college age. Dr. Ames is a co-investigator on Dr. Werch's grant "A Selective Preventive Intervention for High School Seniors," and also has obtained a grant from the Lance Armstrong Foundation, "Brief office intervention to improve the quality of life of prostate cancer patients with biochemical recurrence."

Ethnic and Racial Differences
Drs. G. Croghan, I. Croghan, Hurt, Loprinzi and others have submitted a manuscript titled A Comparison by Ethnicity of a 15 mg/16 Hour Nicotine Patch Alone Versus Nicotine Nasal Spray Alone Versus Both. The purpose of this report was to compare the smoking abstinence in smokers of different ethnic backgrounds (Caucasian versus non-Caucasian) using nicotine patch and/or nicotine nasal spray. This study showed that minorities were less likely to be married (51 percent versus 64 percent, minorities to Caucasians, respectively), more likely not have graduated from high school (15 percent versus 5 percent, respectively), were smoking fewer cigarettes per day at baseline (21 versus 27, respectively), were less likely to have had past quit attempts (79 percent versus 86 percent, respectively), and were more likely to have had a personal history of depression (30 percent versus 20 percent, respectively). A significant difference in smoking abstinence was noted between minorities and Caucasians at the end of treatment (11 percent versus 22.2 percent, respectively) and end of study (4 percent versus 9 percent, respectively).

Surgical Patients
David Warner, M.D., a collaborator from the Department of Anesthesiology, has a developed line of research in tobacco dependence in surgical patients including an international collaboration in a survey of Japanese physicians on perioperative tobacco use interventions. Through a project, "Smoking and Stress in the Perioperative Period," funded by the Minnesota Partnership for Action against Tobacco, Drs. Warner, Ames and Christi Patten, Ph.D., determined that nicotine replacement therapy is not always needed to manage nicotine withdrawal or stress in smokers undergoing surgery. This has led to a line of research in surgical patients who are smokers. Through intramural funding, Drs. Warner, Hurt, and I. Croghan investigated the occurrence of coughing after a smoker stops smoking and found that an increase in coughing after stopping smoking is not common among otherwise healthy patients. Dr. Warner also has ongoing research on the preoperative use of nicotine lozenges to reduce nicotine withdrawal in smokers and the use of nicotine nasal spray to prevent postoperative nausea and vomiting in smokers undergoing surgery. Dr. Warner has a funded R03 grant, "Elective Surgery as a Teachable Moment for Smoking Cessation," and another peer-reviewed grant from ClearWay Minnesota entitled, "Tobacco Helpline in Surgical Patients who are Smokers."

Tobacco Document Research
The Minnesota Tobacco Trial of 1998 resulted in the release of over 50 million pages of previously secret tobacco industry documents and has dramatically changed the field of tobacco control. Over 450 peer-reviewed papers have now been published based on these documents, most of which have been funded by the National Cancer Institute. Dr. Hurt successfully renewed his tobacco document research grant, "Tobacco Industry Documents on ETS - The Next Front," and added Dr. Ebbert as a co-investigator in 2007 along with Monique Muggli. Based on the worldwide nature of the tobacco epidemic and the connection between British American Tobacco and its subsidiary, Souza Cruz, in Brazil, the renewed grant includes a collaboration with Analice Gigliotti, M.D., a colleague in Rio de Janeiro. This research will allow the investigators to identify the scope of the Brazilian tobacco industry's campaign against environmental tobacco smoke (ETS) and define its role in producing genetically-altered tobacco and smuggling. In addition Drs. Hurt and Ebbert and Ms. Muggli reported on the tobacco industry's efforts to eliminate polonium from cigarettes and eventually to suppress the fact that this could not be done in a publication entitled "Waking a sleeping giant: the tobacco industry's response to the polonium-210 issue." This team is leading a collaborative effort with Kelley Lee, D.Phil., also a National Cancer Institute-funded tobacco document researcher of the London School of Hygiene and Tropical Medicine, in an extensive assessment of smuggling of cigarettes into Africa by the industry and what cigarette manufacturers have done to thwart smoke-free workplace policies in China and Spain.

Genetic Epidemiology and Risk Assessment Program
Dr. Ebbert has developed extensive collaborations with investigators in the Genetic Epidemiology and Risk Assessment Program. Along with GERA Program collaborators Ping Yang, M.D., Ph.D.; James Cerhan, M.D., Ph.D.; and Mariza de Andrade, Ph.D.; he is researching various aspects of lung cancer risk reduction after smoking cessation from the Iowa Women's Health Study. Dr. Ebbert also has worked with Dr. Yang on a number of other projects, including alpha1-antitrypsin and lung cancer risks and the glutathione metabolic pathway in lung cancer.

Minnesota Tobacco Control Research and Policy Center
The breadth of expertise in tobacco research, treatment, and education at the University of Minnesota and Mayo Clinic is unique in the world and represents an unparalleled opportunity to create a world class tobacco control multidisciplinary research team that seeks to have high prominence as the leader in the field. Together the institutions are developing the Minnesota Tobacco Control Research and Policy Center, co-led by Drs. Hatsukami and Hurt, to promote collaborative and strategic scientific investigations and to translate these findings into policies, programs, and educational endeavors in order to prevent tobacco related disease and reduce tobacco use in Minnesota, the United States, and globally.

Specifically, this center will:

  • Develop unified and common goals among investigators and with community members
  • Provide an infrastructure that promotes communication and collaboration
  • Increase the number of interdisciplinary research teams and amount of research funding
  • Promote training of students and career development of young faculty
  • Promote communication of our results to other scientists, tobacco control advocates, health care program directors, and policy makers with the goal of bringing national and international visibility and prominence to our center and the University of Minnesota and Mayo Clinic
  • Facilitate the translation of our research so that our findings would affect changes in policies, programs, and be used to educate health care professionals that will positively affect public health
  • Create a strong global presence through training and research

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.