FUNDED BY THE STUART SCOTT MEMORIAL CANCER RESEARCH FUND WITH SUPPORT FROM BRISTOL MYERS SQUIBB
Heart disease and low blood counts are common complications for men with prostate cancer. There are some reasons why this might happen that are already known – either because of the cancer itself or because of some of the treatments for cancer. Recently, scientists have found that white blood cell clones (cells that all come from one cell; called CHIP) have changes in their DNA that might put people at higher risk for heart disease, complications with blood counts, and death. CHIP, like prostate cancer, is associated with age, and may be contributing to heart disease and blood count problems we see in men with prostate cancer. This study will look to see if men who have CHIP with prostate cancer have worse outcomes and if new treatments for prostate cancer contribute to CHIP.
FUNDED BY THE STUART SCOTT MEMORIAL CANCER RESEARCH FUND WITH SUPPORT FROM BRISTOL MYERS SQUIBB
Lung cancer is the leading cause of cancer deaths in the United States. Non-small cell lungcancer (NSCLC) accounts for the majority of lung cancer diagnoses and has a very low survivalrate. There is a sub-population of cells within NSCLC tumors called cancer stem cells (CSCs)that are highly aggressive. These CSCs are capable of fueling the growth and metastasis oftumors and have been shown to be resistant to current drug treatments for NSCLC. Therefore,CSCs must be eliminated to effectively treat and gain lasting remission in patients with NSCLC.CSCs can communicate with other cells in a tumor by transferring information packaged withinsmall particles called extracellular vesicles (EVs). We hypothesize that the molecules packagedwithin EVs from CSCs can make non-CSCs within NSCLC tumors more aggressive by increasing their ability to grow and metastasize. We propose to identify the molecules packaged within NSCLC CSC EVs. We also aim to block the function of the molecules within the CSC EVs to prevent the growth of NSCLC cancer cells. Completion of these studies will provide newinformation about how CSCs function to make NSCLC deadly. In addition, these studies will help in the design of new strategies to eliminate NSCLC CSCs which may provide effective, long-term treatment for NSCLC patients.
FUNDED BY THE STUART SCOTT MEMORIAL CANCER RESEARCH FUND WITH SUPPORT FROM BRISTOL MYERS SQUIBB
Immune cell-based therapies represent the latest pillar of cancer therapy. Chimeric antigen receptor (CAR)-T cells have demonstrated significant anti-tumor activity against B cell leukemia and lymphoma and similar efficacies against multiple myeloma. CAR-NK cells are a newer addition to the cellular immunotherapy field but have already shown impressive results in the treatment of lymphoma. In this project, we will evaluate the activity of CAR-T and CAR-NK cell therapies targeting BCMA and TnMUC1 as single agents and combination strategies for the treatment of multiple myeloma. In addition, we will develop methods to enhance the efficacy and persistence of NK-cell based therapies through strategies to overcome immunosuppression. Successful completion of this project would generate novel and enhanced therapeutic strategies to treat multiple myeloma with immune cell-based therapies.
African Americans develop a form of blood cancer called multiple myeloma more often than Caucasians. On average, African Americans live less long with it. That may be in part because African Americans take part in clinical trials less often. Clinical trials are studies designed to develop new treatment drugs. Those trials can sometimes help people to live longer with this illness. We are trying to improve how many take part in clinical trials at UNC. We are creating an easier, more comfortable doctors’ office to get care at and take part in trials at UNC. We are making it easier for African American researchers at UNC to work on this important issue. We will make a video that shows what clinical research is. It will show why it can be helpful to take part in research. The video will be shown to African Americans and other patients treated at UNC. The UNC team will compare how many African Americans join multiple myeloma trials before and during this grant. If more African Americans enroll in multiple myeloma trials after the grant begins, it would show that these efforts have helped solve this problem. That may help African Americans with multiple myeloma to live longer. IT will also help make important progress in this research.
Cancer is caused by changes that happen in the genes of cancer cells. Special tests can find genes that start or promote cancer growth. New drugs can target cancer causing genes and kill cancer cells. The Duke project team wants to increase awareness and use of both the special tests and the new drugs.The project will bring a group of experts together to talk about patient cases and help find the best medicine for patients. If medicines are not available, the project team can find clinical trial options for patients. The team will also provide training to doctors and nurses on new tests for cancer genes and medicines. We will create information to help patients learn about the special gene tests and how the results can help the doctors choose the right medicine to treat their cancer. When the project is finished,the team hopes to provide the information and tools created to other local doctor’s offices and patients.
There have been significant advances in the treatment of patients living with metastatic breastcancer. Some of these advances are due to a fairly new type of technology looking at changes inthe DNA of the tumor (somatic next-generation sequencing (NGS)) and/or in patient’s normal cells(germline NGS) that may impact a patient’s prognosis and/or treatment options, including theopportunity to enroll on clinical trials.
Very few studies have looked at patient understanding and knowledge on this type of advancedtesting (next-generation sequencing), though of the studies available, there appears to be a lowlevel of patient knowledge on next-generation sequencing and a gap in expectations as to howthis form of testing can impact a patient’s clinical care.
The aim of our study is to increase the enrollment of patients with metastatic breast cancer intoclinical trials that match patients to specific therapies based on their NGS through 1) increasingpatient knowledge and understanding of NGS and 2) using the education tool to identify thechange in the rate of NGS testing, as well as change of treatment recommendations based onthese results.
African Americans have the highest percentage of new cancer cases in the United States and the worst outcomes. Other diverse populations have difficulty getting to a cancer treatment center or need help figuring out the system one they arrive. Some people die from cancers that can be prevented or treated, simply because they are not aware of all of the treatment options. Cancer care can be very difficult because many times a patient has more than one doctor who is part of their care team. This can be scary and may make some people choose not to get cancer treatment, even if they can be cured. WFBCCC wants to make sure that everyone has access to the best cancer care possible. This may include patients participating in research that may improve outcomes for them but also may help provide information that can help tailor treatments for the next generation of cancer patients. It is important to make sure all populations are represented in studies that look at new treatments or supports for cancer patients. To meet that goal, we created a population health navigator program- people who are from the community who can help people learn about cancer, how to prevent it, what screening is required and what treatments are available. If someone is diagnosed with cancer, the navigator will assist that person by helping to remove barriers to care and will talk with patients about clinical research as part of their care.
Clinical trials test new treatments for patients. Clinical trials also help doctors learn what type of treatments work best for what patients. It is important for patients to participate in clinical trials so that we can continue to develop new treatments and improve the care of cancer patients. Very few adult patients with cancer join clinical trials. Black patients participate in trials less than white patients. We have learned several of the reasons that black patients are less likely to join clinical trials. Using what we have previously learned we will create an educational brochure designed specifically for black patients with breast cancer to see if it helps address some of the unique concerns black women have about joining clinical trials.
One in every eight women will be diagnosed with breast cancer in a lifetime. But it doesn’t impact everyone equally. While Caucasian women are more likely to be diagnosed with breast cancer, African- American (AA) women are more likely to die from the disease. In addition, AA women are more likely to be diagnosed at a younger age and have a more aggressive form of breast cancer. There have been many improvements in the treatment of breast cancer leading to a lower chance of dying from the disease. But AA women have not been shown to benefit as much as Caucasian women from these advancements. There are many factors believed to be the reason for this racial difference in survival. But there is a need for more research into this area. One way to better study these factors is within the context of a clinical trial. AA women are historically less likely to be in a cancer clinical trial study. This proposed study is aimed at increasing the enrollment of AA female breast cancer patients in clinical trials at UCSD by creating a clinical trial education program to both educate and engage the community. This is predicted to lead to a decrease in the current breast cancer survival disparity.
This goal of this project is to develop a new mobile application that will bring together multiple useful functions that will help breast cancer patients who are considering or participating in clinical trials. There are various applications in the market that may do one specific function but very few integrate both patient education resources with tools to help patients manage their participation on clinical trials. This includes keeping track of medication compliance, appointments, and side effects. All of these patient reported outcomes are critical for the successful completion of a clinical trial. A tool that can provide both information to breast cancer patients while helping them be compliant with the clinical trial needs could be a valuable tool as more patients depend on their smartphones and mobile devices on a daily basis.
