22nd Cancer Center Annual Symposium & Workshop

"Turning Data into Knowledge, & Knowledge into Health"

 October 28 - 30, 2024

Charleston, SC


(All new attendees receive one year society membership)

Register Today

Welcome to

 

Cancer informatics
for Cancer Centers

 


The Cancer Center Informatics Society: “Turning Data into Knowledge, & Knowledge into Health ®”


For over a decade, Ci4CC has served as a vital platform for professionals in precision oncology, data science, and cancer informatics, fostering collaboration and development. As a hub for applied innovation, it has made a profound impact on policy, oncology research and patient care, driving new insights and reshaping our understanding of cancer. 


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Cancer Center Headlines & Publications

By Sorena Nadaf 04 Sep, 2024
American Cancer Society and Color Health to Provide Free At-Home Colorectal Cancer Screening in Underserved Rural Communities
04 Sep, 2024
Leading Progress Against Cancer
24 Aug, 2024
By Drs Karen Knudsen & Othman Laraki.
By Sorena Nadaf 18 Jul, 2024
Conversation with The Cancer Letter: NCI’s new chief data scientist Warren Kibbe tells us about efforts to get “AI-ready” - July 12, 2024
By Sorena Nadaf 11 Jul, 2024
"Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States, 2019" American Cancer Society
29 May, 2024
The UCSF Division of Clinical Informatics and Digital Transformation (DoC-IT) and UCSF Health have received a $5 million gift from Ken and Kathy Hao to develop a cutting-edge, real-time, continuous, and automated artificial intelligence (AI) monitoring platform for clinical care. The Impact Monitoring Platform for AI in Clinical Care (IMPACC) aims to bridge the gap between the rapid evolution of AI technologies used by clinicians and the essential need for robust, ongoing assessment of their efficacy, safety, and equity. Julia Adler-Milstein, PhD , chief of the UCSF Division of Clinical Informatics and Digital Transformation (DoC-IT), and Sara Murray, MD, MAS , chief health AI officer at UCSF Health, will lead the pioneering collaboration. “This philanthropic gift is transformative in many ways,” said Adler-Milstein. “It comes at a critical juncture as the healthcare industry more broadly integrates AI into clinical practice. Through IMPACC and this collaborative effort, we are poised to improve patient care at UCSF while advancing the science of how to assess AI tools in real-world use.” Currently, the healthcare field lacks established protocols for ongoing AI monitoring, leading to risks of adverse outcomes for patients and healthcare providers that go undetected. While assessments are conducted to determine the suitability of new AI technologies for safe integration into clinical environments before deployment, once they are deployed, health systems need a way to promptly identify any issues in their real-world performance. IMPACC will fill this urgent need by shifting from planned, periodic, manual monitoring of a focused set of measures to real-time, continuous, automated, and longitudinal monitoring across a broad measure set with specified criteria for escalation to human review and intervention.  Full Article: https://docit.ucsf.edu/news/ucsf-and-ucsf-health-receive-pivotal-donation-support-first-continuous-ai-monitoring-platform
By Sorena Nadaf 24 May, 2024
I’m most proud of how my colleagues and I evolved CBIIT’s focus and activities to enable NCI’s scientific mission. My approach had always been to collaborate with colleagues from various NCI divisions, offices, and centers (DOCs). In doing this, we understood each other’s specific needs and ensured that our work together aligned with those needs. This wasn’t always CBIIT’s approach though, and while the change started before I became director, creating the necessary collaborations across the institute and developing the projects to support our scientific partners took consistent and intentional focus. CBIIT has been working closely with the other NCI DOCs for years, supporting individual projects and concerted efforts in major programs (such as the NCI Cancer Research Data Commons [CRDC]), data sharing, and NCI Intramural Research Program data management. In hindsight, I might have tried to initiate this outreach and move these relationships forward more broadly and even more quickly. I also would have ensured that we invested more time and some dedicated funding in innovation. To Article: https://datascience.cancer.gov/news-events/blog/dr-tony-kerlavage-reflects-his-time-nci-cbiit
08 Mar, 2024
The aims of our case-control study were (1) to develop an automated 3-dimensional (3D) Convolutional Neural Network (CNN) for detection of pancreatic ductal adenocarcinoma (PDA) on diagnostic computed tomography scans (CTs), (2) evaluate its generalizability on multi-institutional public data sets, (3) its utility as a potential screening tool using a simulated cohort with high pretest probability, and (4) its ability to detect visually occult preinvasive cancer on prediagnostic CTs.
08 Mar, 2024
Cancer Mutations Converge on a Collection of Protein Assemblies to Predict Resistance to Replication Stress
08 Mar, 2024
International cancer registries make real-world genomic and clinical data available, but their joint analysis remains a challenge. AACR Project GENIE, an international cancer registry collecting data from 19 cancer centers, makes data from >130,000 patients publicly available through the cBioPortal for Cancer Genomics (https://genie.cbioportal.org). For 25,000 patients, additional real-world longitudinal clinical data, including treatment and outcome data, are being collected by the AACR Project GENIE Biopharma Collaborative using the PRISSMM data curation model. Several thousand of these cases are now also available in cBioPortal. We have significantly enhanced the functionalities of cBioPortal to support the visualization and analysis of this rich clinico-genomic linked dataset, as well as datasets generated by other centers and consortia. Examples of these enhancements include (i) visualization of the longitudinal clinical and genomic data at the patient level, including timelines for diagnoses, treatments, and outcomes; (ii) the ability to select samples based on treatment status, facilitating a comparison of molecular and clinical attributes between samples before and after a specific treatment; and (iii) survival analysis estimates based on individual treatment regimens received. Together, these features provide cBioPortal users with a toolkit to interactively investigate complex clinico-genomic data to generate hypotheses and make discoveries about the impact of specific genomic variants on prognosis and therapeutic sensitivities in cancer.
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