Cancer information is widely shared on social media, however not all information is true. We aim to explore how social media designs, including in platform prompts and messages, can encourage individuals in cancer care networks to think about the quality and accuracy of cancer information shared online. This innovative work will establish the feasibility, infrastructure, and protocols to test social media designs (prompts, messages) among adults in cancer care networks.

Purpose: to establish a Registry of pediatric patients treated with proton radiation therapy. Participants: Patients who are less than or equal to 21 years old at time of treatment start and treated with radiation therapy at one of the participating centers. Procedures (methods): This Proton and Photon Consortium Registry (PPCR) enrolls children treated with radiation therapy to form an expansive description of the pediatric population that receives protons and to better catalogue the benefits of protons, in this cohort. The data will also be used to evaluate practice differences and help facilitate collaborative research across the various radiation centers. The PPCR collects an expanded set of demographic and clinical data that will enhance the practice data that many participating radiation centers already collect in their routine operations. The PPCR has been expanded to include a photon-treated control group, helping to facilitate comparative effectiveness analysis.

The goal of this survey is to evaluate othe current practice across institutions in the United States by surveying Pathologists and Pathologists' Assistants about their approach to pathologic evaluation of bladder cancer specimens (cystectomies). This information would provide useful information about best practices for gross examination of post-NAC cystectomies and help standardize practice between institutions.

Cancer is the leading cause of death in the Hispanic population in the U.S. Our study focuses on collecting information to build a cancer registry from a diverse Hispanic population to identify specific cultural and demographic details that will allow us to determine which attribute carries a higher risk of a poor outcome. We will also be utilizing a set of questionnaires and surveys that evaluate the health and functionality of older adults thoroughly and efficiently. These surveys provide a wealth of prognostic data and have been shown to detect deficits even in younger patients. Although the information we hope to collect is of considerable value, we must first examine whether our approach to consenting patients and having them complete these questionnaires is feasible. We anticipate that the findings from our study will provide valuable insights on Hispanic adults with cancer as a unique and growing patient population in the U.S.

The primary objective of the current study is to assess cancer patient perceived barriers to adherence to oral cancer medications. The results of this survey will aid clinicians in identifying targeted priorities in future programs aimed at improving adherence in patients taking oral cancer medications.

The expected outcome of this proposal is a novel care pathway delivered by pharmacists to improve side effects during oral chemotherapy for patients, a known barrier to adherence, and ultimately to prevent progression and early mortality. Our long-term goal for P3OC is to develop and test new dashboard features to optimize pharmacy care and meet future needs for value-based payment models

We are building an automatic pathology report summarization system. We would like to include human judgement from professionals to help us understand and explain the results, and improve the system. In the evaluation, we will schedule a 30-min meeting do go through the details and for the professional to sign a consent form. The professional will expect to receive twenty documents including ten raw reports and ten summaries of these reports. They will be sent in a random order with no correspondence indicated. For each of the document, you will be asked to answer ten questions. We will evaluate the quality of the summaries based on the time she/he spent on reading the report, answering the questions, and the accuracy of the questions.

The purpose of the study is to determine how the Cancer Prevention and Control Research Network (CPCRN) researchers and their community partners are operationalizing the nine health equity Principles adopted by the network. The examples, acquired through in-depth interviews, will be used to develop a technical assistance toolkit for CPCRN and the general research community.

The purpose of this project is to identify and target barriers faced by rural endometrial cancer patients in order to develop a patient navigation intervention. Rural residents with endometrial cancer, the the most prevalent gynecologic cancer in the US, have higher odds of mortality than urban endometrial cancer patients. As the number of new endometrial cancer cases is expected to increase 50% by 2030, this urban-rural disparity is expected to continue widening.

We would like to help patients identify what is important to them, i.e., their values, and support communicating that to their caregivers and healthcare providers. We are trying to create a tool that will make it easier to share what is most important to patients with metastatic breast cancer and their caregivers, with the patient's oncology healthcare provider.