
Trusted Oncology Guidelines Get a Digital Makeover: National Comprehensive Cancer Network Launches NCCN Guidelines Navigator
PLYMOUTH MEETING, Pa., June 24, 2025 /PRNewswire/ -- The National Comprehensive Cancer Network ® (NCCN ®)—an alliance of leading cancer centers—announces a new, interactive digital delivery format for the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines ®). The NCCN Guidelines ® are the recognized standard for clinical decision making and policy in cancer care and are the most thorough and frequently updated clinical practice guidelines available in any area of medicine. They assist in the decision-making process of individuals involved in cancer care and prevention—including physicians, nurses, pharmacists, payers, patients and their caregivers—with the ultimate goal of improving patient care and outcomes.
The new NCCN Guidelines Navigator ™ presents the evidence-based, expert consensus-driven recommendations from the NCCN Guidelines in a virtual platform that allows users to search and navigate more easily. Access to the NCCN Guidelines Navigator™ is available with a free NCCN account for non-commercial use. Features of the NCCN Guidelines Navigator™ include:
"This is truly the future of cancer treatment guidance," said Crystal S. Denlinger, MD, Chief Executive Officer, NCCN. "Cancer prevention, screening, treatment, and supportive care that follows internationally-trusted guidelines has been shown time and again to improve outcomes for people with cancer. I'm proud that we've achieved our ambitious goal for increasing the accessibility and usability of the content from the NCCN Guidelines without compromising any quality."
The NCCN Guidelines Navigator™ recently began beta testing for colon and prostate cancers. That was followed by rectal cancer, which was published on June 16, 2025. NCCN will continue to publish NCCN Guidelines Navigator™ for additional cancer types until all 88 NCCN Guidelines are available in the new format. The original pdf format will also remain available for all NCCN Guidelines. Both forms will feature the most up-to-date information users rely upon for daily use in cancer care and prevention.
People who access the NCCN Guidelines in any format, including via the NCCN Guidelines Navigator™, can earn CE/MOC credit through the new NCCN Guidelines in Practice ™—which was just announced earlier this month.
NCCN also plans to continue to optimize this new tool, including adding artificial intelligence (AI) capabilities to make searching even more conversational and intuitive, plus increased integration with NCCN's other resource offerings.
"It has been 30 years since we first launched the NCCN Guidelines; since then, they have come to be used by millions of people worldwide every year, including more than 90% of U.S. and global physicians surveyed," said Dr. Denlinger. "Cancer care is becoming increasingly effective but also more complicated every year. The new NCCN Guidelines Navigator tool simplifies the evolving evidence from the latest research, leverages expertise to put it into context, and places it at the point-of-care for decision-making support and education. This new resource integrates everything we do to support people with cancer and their care providers by defining and advancing quality, effective, equitable, and accessible cancer care and prevention so all people can live better lives."
Visit NCCN.org/navigator for more information.
About the National Comprehensive Cancer Network
The National Comprehensive Cancer Network ® (NCCN ®) is marking 30 years as a not-for-profit alliance of leading cancer centers devoted to patient care, research, and education. NCCN is dedicated to defining and advancing quality, effective, equitable, and accessible cancer care and prevention so all people can live better lives. The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines ®) provide transparent, evidence-based, expert consensus-driven recommendations for cancer treatment, prevention, and supportive services; they are the recognized standard for clinical direction and policy in cancer management and the most thorough and frequently-updated clinical practice guidelines available in any area of medicine. The NCCN Guidelines for Patients ® provide expert cancer treatment information to inform and empower patients and caregivers, through support from the NCCN Foundation ®. NCCN also advances continuing education, global initiatives, policy, and research collaboration and publication in oncology. Visit NCCN.org for more information.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Korea Herald
2 days ago
- Korea Herald
Esaote presents at ECVS 2025 the new generation of veterinary MRI, Vet -MR Grande ELITE
GENOA, Italy and ANTWERP, Belgium, July 3, 2025 /PRNewswire/ -- Esaote, a leading company in the field of medical diagnostic imaging, presents the new Vet -MR Grande ELITE, the next generation of veterinary MRI at the ECVS 2025, the Annual scientific meeting of European College of Veterinary Surgeon in Antwerp, Belgium held on July, 3-5 (Esaote Booth n. 32). Born from decades of expertise and developed in close collaboration with top veterinary clinics worldwide, the Vet-MR Grande ELITE is a revolutionary imaging solution tailored for both small animals and equines, which responds to the continuous evolution of market needs in terms of technologies, workflows and advanced imaging capabilities. "Putting our customers first is the driving force behind our innovation at Esaote," said Erminio Bassi, Esaote Vet Business Manager."The Vet-MR Grande ELITE builds on the proven success of the Vet-MR Grande, bringing smarter technology, greater sustainability, and introducing a suite of innovations designed to elevate the standards of veterinary imaging, with the aim of delivering outstanding image quality, enabling clearer, more reliable diagnoses." Developed in partnership with AIRS Medical, the advanced AI-powered platform e-SPADES enhances image reconstruction and scan efficiency. It enables shorter examination times compared to conventional methods while delivering exceptional image quality to support veterinary diagnostics with greater precision. The Diffusion Weighted Imaging (DWI) sequence plays a key role in enhancing neurological examinations. It enables improved detection of cerebral infarction, stroke, and brain tumors, while supporting their classification, grading, and ongoing monitoring. Purpose-built for the realities of veterinary practice, the Vet-MR Grande ELITE features an intuitive interface tailored to animal anatomy, complete with species-specific tools and expert-developed protocols. Its open design, large patient table, and dedicated coils allow for quick, comfortable positioning—while also simplifying anesthesia management. Thanks to its compact, energy-efficient design, the system offers a sustainable and cost-effective solution that operates on a standard power supply—making advanced MRI more accessible from small practices to large referral centers. Esaote Group Leader in medical imaging (ultrasound, MRI, software to manage the diagnostic process). At the end of 2024, the Group had approximately 1,300 employees, half of whom in Italy. With facilities in Genoa and Florence, and its own production and research units in Italy and the Netherlands, Esaote maintains a presence in over 100 countries around the world.
![[iNtRON] Files U.S. Patent for Three Novel Endolysin-Based Drug Candidates Targeting Gram-Negative Bacteria](/_next/image?url=https%3A%2F%2Fall-logos-bucket.s3.amazonaws.com%2Fkoreaherald.com.png&w=48&q=75)
Korea Herald
3 days ago
- Korea Herald
[iNtRON] Files U.S. Patent for Three Novel Endolysin-Based Drug Candidates Targeting Gram-Negative Bacteria
BOSTON and SEOUL, South Korea, July 2, 2025 /PRNewswire/ -- More than 1,200 reported cases of CRE (Carbapenem-Resistant Enterobacteriaceae) infections have been reported in the In-cheon region of South Korea alone between January and April of this year. In addition, in June of this year, a report was released that an investigation had begun into Salmonella infections linked to eggs across seven U.S. states. These and other ongoing reports are raising awareness about the dangers of CRE, a representative Gram-negative bacterium, as infections caused by Gram-negative bacteria are becoming an increasingly serious global issue. Amid the growing trend of infectious disease outbreaks caused by Gram-negative bacteria, we have determined that it is time to move forward with the commercialization of related technologies. Accordingly, we have recently completed U.S. patent applications for three novel endolysin-derived drug candidates showing strong antibacterial activity against Gram-negative and superbugs. These newly patented drug candidates — PKL200, TSL2200, and EAL2200 — were derived from the GN200 development program that has been carried out over the past several years using the proprietary platform technology we named "itLysin." The drug candidate PKL200 demonstrates strong bacteriolytic activity against several major Gram-negative bacteria, including Acinetobacter baumannii, Pseudomonas aeruginosa, Klebsiella pneumoniae, Klebsiella aerogenes, and Enterobacter cloacae, including CRE. It also exhibits antibacterial activity against Uropathogenic Escherichia coli (UPEC), which is one of the major causes of urinary tract infections (UTI). PKL200 is considered a highly promising drug candidate with potential for treating various indications, including intestinal CRE clearance, pneumonia, and urinary tract infections. Another drug candidate, TSL2200, is a pipeline that offers rapid bactericidal effects against all types of Salmonella. It is expected to be used to prevent and treat Salmonella infections caused by contaminated eggs, meat, salads, tomatoes, and other foods. Its potential applications extend to the dairy, meat processing, and broader food processing industries, as well as being a treatment for food poisoning. EAL2200 is a pipeline that provides antibacterial activity against bacteria of the Erwinia genus, which cause bacterial diseases in fruit crops, including fire blight. In a situation where there are currently no safe and effective treatments for fire blight, this pipeline is expected to be used as a bio-control agent and therapeutic with biological safety for both the environment and human health. All of the newly patented drug candidates were developed through the itLysin platform, an advanced endolysin technology derived from our long-standing expertise in bacteriophage and endolysin technologies. Traditional antibiotics and other drugs have shown limited effectiveness against Gram-negative bacteria due to the outer membrane barrier. However, the drug candidates developed through the itLysin platform have been designed to more efficiently penetrate the outer membrane structure of Gram-negative bacteria, thereby overcoming the limitations of existing drugs and technologies. This patent application was not merely for the purpose of securing rights but was a strategic decision focused on commercialization. While it was common in the past to file patents first and then seek commercialization opportunities, this time, the patents were filed based on thorough commercialization preparations. This is a strategy that effectively secures rights to the drug candidates and is advantageous in terms of technology security. We are leading the development of new drugs against super bacteria based on our proprietary bacteriophage and endolysin technologies, and we have secured multiple promising pipelines. Recently, we have presented our commercialization strategy through press briefings and corporate presentations. With global pharmaceutical companies showing significant interest due to the lack of effective antibiotics against Gram-negative bacteria worldwide, we plan to accelerate the development of pipelines targeting Gram-negative bacteria based on these recent patent applications. We will continue our efforts to achieve tangible results through various commercialization strategies. it is iNtRON.


Korea Herald
4 days ago
- Korea Herald
Seegene Launches STAgora™, a New Platform for Infectious Disease Analytics
SEOUL, South Korea, July 1, 2025 /PRNewswire/ -- Seegene Inc., a global leader in molecular diagnostics (MDx) solutions, announced today the launch of STAgora™, a next-generation platform for infectious disease analytics. Designed as a real-time infectious disease intelligence system, the platform combines diagnostic data with advanced statistical modeling and aims to redefine how the world detects, tracks, and responds to outbreaks. STAgora™ provides real-time global visualization of infectious disease trends at the municipal, national, and continental levels, based on actual diagnostic test results. The platform delivers healthcare professionals immediate, structured diagnostic reports and statistical analyses in clear, actionable formats. These are supported by customizable dashboards and real-time alert functions. In addition to tracking individual cases, STAgora™ enables users to monitor outbreaks across selected regions, both local and international. This capability provides real-time visibility into disease spread, enhancing situational awareness and supporting timely, data-driven public health responses. By equipping national and global health authorities with real-time epidemiological insight, the platform is expected to strengthen decision-making and support the development of effective response strategies to mitigate large-scale infectious disease outbreaks. With more than 40 built-in statistical tools, STAgora™ enables early detection of abnormal pathogen patterns and supports predictive modeling for seasonal trends and emerging outbreaks. These tools include modules for tracking individual infections, analyzing symptom-based co-infections and calculating real-time infection rate trends. Together, they help transform static data into forward-looking intelligence that guides proactive interventions. Unlike traditional outbreak monitoring systems that rely on retrospective data, STAgora™ performs real-time analysis of PCR-derived diagnostics. This allows for immediate visibility into pathogen spread and, through AI-based algorithms, the forecasting of potential future outbreaks. "The key differentiator of STAgora™ is its unique architecture, which aggregates real-time diagnostic data from around the world into a unified analysis platform," said Young-Seag Baeg, head of strategic planning at Seegene. When paired with Seegene's proprietary syndromic quantitative PCR technology, STAgora™ offers expanded visibility into both single-pathogen infections and simultaneous multi-pathogen co-infections. This comprehensive diagnostic insight empowers clinicians to make faster, more informed decisions at the point of care. "During the COVID-19 pandemic, we saw firsthand how crucial accurate and timely interpretation of diagnostic data was in shaping public health policies and clinical outcomes," said Daniel Shin, executive vice president and chief global sales and marketing officer at Seegene. "Now, as we confront increasingly complex threats such as antimicrobial resistance, viral mutations and co-infections, the ability to deliver actionable insights from diagnostic data is becoming a cornerstone of clinical innovation and a vital pillar of global health security." Seegene will officially debut STAgora™ at the 2025 Association for Diagnostics & Laboratory Medicine (ADLM) annual meeting, taking place July 27 to 31 in Chicago, USA. The event will highlight key capabilities of the platform, including its integration with CURECA™, Seegene's fully automated, unmanned PCR system. ADLM 2025 will also serve as a launchpad for Seegene to explore global collaboration and partnerships with healthcare leaders and clients. With the launch of STAgora™, Seegene aims to lay the foundation for a smarter, faster and more connected global health defense system. By combining real-time molecular diagnostics, AI-driven analytics and global data integration, STAgora™ represents a strategic step toward building an intelligent public health infrastructure capable of responding proactively to emerging threats. The company envisions the platform as a core pillar of the global infectious disease response framework, marking a new step toward enhanced diagnostic insight and preparedness. About Seegene Seegene has more than 20 years of dedicated experience in R&D, manufacturing, and business related to syndromic real-time PCR technologies. This expertise was particularly highlighted during the COVID-19 pandemic when Seegene provided over 340 million COVID-19 tests to more than 100 countries worldwide. The core feature of Seegene's syndromic real-time PCR technology is the ability to simultaneously test for 14 pathogens that cause similar signs and symptoms in a single tube with quantitative information. CURECA™(Continuous, Unlimited, Random-access, Expandable, and Customizable Automation) is a fully automated and modular PCR system that eliminates manual processes and enables continuous, real-time testing. It is a unified platform designed to operate continuously, 24 hours a day, with no human intervention. The very core feature is CPS which is the first part of CURECA™, the world's first automated pre-treatment system capable of handling a full spectrum of specimen types, including blood, stool, sputum, and urine. Designed to support both centralized and decentralized labs, CURECA offers scalable automation and flexible adoption—making it especially valuable in settings with limited space or personnel.