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National Comprehensive Cancer Network

The National Comprehensive Cancer Network (NCCN) is a not-for-profit of 33 leading cancer centers in the United States, founded in 1995 to define and advance quality, effective, equitable, and accessible cancer care and prevention. Comprising multidisciplinary teams of experts, NCCN focuses on improving patient outcomes through evidence-based clinical practice guidelines, research programs, and educational initiatives that support clinicians, patients, and healthcare decision-makers worldwide. NCCN's cornerstone activity is the development of its Clinical Practice Guidelines, which provide consensus-driven recommendations covering prevention, screening, diagnosis, treatment, and supportive care for 97% of cancers encountered in clinical practice. These guidelines are created by 63 specialized panels involving over 1,900 clinicians and researchers from NCCN member institutions, incorporating the latest evidence from clinical trials and expert consensus, with continuous updates to reflect new data. First published in 1996 for major cancer types such as , colon, , and others, the guidelines have evolved into a global standard, surpassing 16 million downloads by 2025 and influencing practices worldwide. In addition to guidelines, NCCN pioneered the multidisciplinary approach to cancer care, emphasizing among physicians, nurses, pharmacists, and other specialists to optimize treatment plans. The also advances through its Oncology Research Program, established in 1999, which funds and supports investigator-initiated clinical trials, and provides patient-facing resources like simplified guideline versions and tools for shared decision-making. Through its member institutions—initially 13 at founding and expanded over decades—NCCN ensures access to cutting-edge treatments while promoting quality and safety initiatives that enhance equitable cancer care globally.

History

Founding

The National Comprehensive Cancer Network (NCCN) was established in January 1995 as a not-for-profit of leading cancer centers, announced at a press conference in on January 31. The organization's original purpose was to develop national standards for the delivery of cancer care and to conduct outcomes-based research aimed at providing high-quality, cost-effective services to patients nationwide. The founding consortium consisted of 13 premier cancer institutions, selected for their expertise in multidisciplinary cancer care and research. These original members were: appointments followed soon after the announcement, with Bruce R. Ross named as the first and Joseph V. Simone, MD, appointed as the inaugural Chair of the , both in 1995. At inception, the NCCN faced challenges in demonstrating the value of comprehensive cancer centers to payers and policymakers, particularly countering perceptions that academic institutions were more expensive than community hospitals and lacking robust data on clinical and cost-effectiveness beyond simplistic metrics.

Key Milestones and Expansion

The National Comprehensive Cancer Network (NCCN) marked a significant early in 1996 with its inaugural Annual Conference, which drew over 300 attendees and facilitated discussions on advancing cancer care standards. That same year, NCCN published its initial set of clinical practice guidelines, covering key malignancies such as and , establishing a foundation for evidence-based recommendations. In 1998, NCCN expanded its digital presence by launching the NCCN.org website, providing broader access to its resources and fostering among member institutions. By 2003, the organization further solidified its role in with the introduction of the Journal of the National Comprehensive Cancer Network (JNCCN), a peer-reviewed publication dedicated to research, guidelines, and policy. A pivotal expansion occurred in 2010, when the NCCN Foundation was established to support and initiatives. Also in 2010, NCCN released its first Guidelines for Patients, translating complex clinical recommendations into accessible language for individuals affected by cancer. Throughout its history, NCCN has grown substantially in institutional reach, expanding from 13 founding member centers in 1995 to 33 leading cancer institutions by 2025, enhancing its influence on national and global cancer care. Reaching a notable benchmark in 2025, the NCCN Guidelines surpassed 16 million downloads worldwide, reflecting their widespread adoption by clinicians and patients. That year also saw the launch of innovative digital tools, including the NCCN Guidelines Navigator™ for streamlined guideline navigation and the Guidelines in Practice™ program to support practical implementation in clinical settings.

Mission and Organizational Structure

Mission and Objectives

The National Comprehensive Cancer Network (NCCN) operates under an official to define and advance quality, effective, equitable, and accessible cancer care and prevention so all people can live better lives. This mission underscores NCCN's commitment to establishing standards that ensure comprehensive, evidence-based approaches to , addressing both treatment and preventive strategies across diverse populations. NCCN's core objectives focus on improving the quality, effectiveness, and efficiency of cancer care within practice. These include promoting multidisciplinary team approaches that integrate expertise from various medical disciplines to optimize outcomes, as well as contributing to ongoing and initiatives that disseminate best practices globally. By developing resources such as clinical practice guidelines, NCCN aims to support stakeholders including clinicians, , and policymakers in making informed decisions that enhance care delivery. The organization's vision is to achieve access to high-quality, high-value, patient-centered cancer care for all people on a global scale. This vision aligns with NCCN's mission, which emphasizes equity in addressing disparities and accessibility to ensure resources reach underserved communities. It is further guided by core values of excellence, collaboration, respect, integrity, passion, and innovation. These core values drive NCCN's efforts to foster ethical, transparent, and forward-thinking advancements in the field. NCCN has played a pioneering role in the development of multidisciplinary care models for , integrating collaborative strategies that prioritize holistic patient management over siloed approaches. This foundational emphasis on team-based care has influenced modern by promoting integrated , , and clinical protocols that adapt to evolving .

Governance and Leadership

The National Comprehensive Cancer Network (NCCN) operates as a not-for-profit of 33 leading cancer centers dedicated to advancing cancer care, , and . The NCCN , the primary decision-making body, consists of 66 members, with two representatives from each member institution, ensuring collaborative input on strategic directions. The board is chaired by Matt Kalaycio, MD, FACP, from the Case Comprehensive Cancer Center/University Hospitals Seidman Cancer Center and Taussig Cancer Institute. Overseeing day-to-day operations and implementing board policies is the Executive Committee, composed of 10 members, including the board chair. Additional standing committees support specific functions, such as the Finance Committee, which manages fiscal responsibilities and is chaired by Patrick J. O'Brien, MBA, from ; and the Governance Committee, which handles nominations and bylaws, chaired by Christopher H. Lieu, MD, from the Cancer Center. As (CEO) since 2023, Crystal S. Denlinger, MD, leads the organization's overall strategy and programs; she joined NCCN in 2021 as Senior and previously served at . The Senior Management Team supports the CEO in executing operations, with key roles including Gary J. Weyhmuller, MBA, SPHR, as Executive and ; Eileen C. Boscia, , MBA, as and ; Kristina M. Gregory, , , as Senior of Clinical Information; Jennifer Tredwell, MBA, as Senior of Marketing and Communications; Beth Gaffney, MBA, as of U.S. and Global Business Development; and Alyssa Schatz, DrPH, MSW, as of Policy and Advocacy. The NCCN Foundation, a supporting entity, has a separate with 13 members, chaired by Gena Cook from Kaliper Health, focused on fundraising to develop resources such as the NCCN Guidelines for Patients.

Clinical Practice Guidelines

Development Process

The development of NCCN Clinical Practice Guidelines involves multidisciplinary panels composed of experts from its 33 member institutions, including over 1,900 clinicians, researchers, and patient advocates specializing in specific cancer types or supportive care areas. These panels, led by a chair and vice chair, integrate physicians, nurses, and other subspecialists to ensure comprehensive perspectives on preventive, diagnostic, therapeutic, and supportive care recommendations. Participation is voluntary and funded solely by member institution dues, with no industry support influencing the process. The guidelines follow an evidence-based methodology, beginning with systematic reviews of , including searches for clinical trials and emerging data, combined with expert clinical judgment and institutional feedback. Recommendations are formulated as algorithms and flowcharts to guide , supported by discussion sections that reference key studies and rationale for each pathway. External submissions for consideration are accepted through a public portal, ensuring transparency in incorporating new evidence. To maintain integrity, NCCN enforces strict policies, requiring all panel members to disclose financial relationships annually, with recusal from discussions or votes on topics involving meaningful conflicts (defined as over $20,000 from a single entity or $50,000 aggregate). These disclosures are publicly available, and panels operate under a "" policy that prohibits pre-release communications with non-members and excludes individuals with significant conflicts from participation. The process is consensus-driven, with panel meetings involving structured discussions and voting on recommendations; outcomes are categorized by evidence strength and agreement level (e.g., Category 1 requires at least 85% with high-level ). documents detail meeting summaries, vote results, change rationales, and supporting references for each update. Guidelines undergo annual comprehensive reviews by the panels and multidisciplinary faculty at each member institution, with interim updates issued as needed for significant new evidence or regulatory changes, ensuring recommendations remain current. Each version includes panel member affiliations, specialties, full algorithms, discussion text, and bibliographies of referenced data.

Content and Accessibility

The NCCN produces several types of clinical resources, including the professional NCCN Guidelines® designed for oncologists and other clinicians, patient-friendly Guidelines for Patients that translate complex recommendations into accessible language, and the NCCN Drugs & Biologics , which offers evidence-based guidance on the appropriate use of drugs and biologics in . These resources collectively cover more than 60 cancer types and subtypes, encompassing nearly every major , along with principles for supportive care, genetic , and survivorship , addressing over 97% of individuals diagnosed with or at risk for cancer in the United States. The guidelines are presented in structured formats, featuring algorithms and flowcharts for visual decision-making pathways, supplemented by detailed text-based discussions, references, and evidence summaries to support clinical reasoning. These materials are distributed across multiple platforms, including editions, the NCCN for online viewing, and dedicated mobile applications that enable on-the-go access for healthcare providers. Accessibility is a core principle, with professional NCCN Guidelines® available at no cost to registered users via the NCCN website and apps, while Guidelines for Patients are freely downloadable in PDF format without registration to empower patients and caregivers. In 2024, these resources achieved more than 16 million downloads annually, reflecting widespread adoption among global users, approximately 48% of whom are international. NCCN maintains high web accessibility standards to ensure equitable use across diverse needs, including support for assistive technologies. To address time-sensitive updates, NCCN provides Flash Updates™, a subscription-based notification service highlighting recent changes to guidelines and compendia, ensuring clinicians receive alerts on evolving evidence. Additionally, the NCCN Guidelines Navigator™ serves as an interactive digital tool integrated with the guidelines, allowing users to search, filter, and navigate content efficiently for streamlined decision-making.

Member Institutions

Overview and Criteria

The National Comprehensive Cancer Network (NCCN) member institutions represent a select alliance of leading cancer centers , primarily focused on advancing patient care, , and in . These institutions specialize in managing complex, aggressive, and rare cancers, providing multidisciplinary approaches that integrate cutting-edge treatments and clinical trials. Collectively, they handle more than 160,000 new cancer patients annually, serving as hubs for innovative therapies and equitable access to high-quality care. Membership in the NCCN is reserved for institutions that meet stringent standards of excellence, typically requiring designation as (NCI)-designated comprehensive cancer centers or equivalents that demonstrate superior performance in multidisciplinary patient care, research innovation, and outcomes measurement. All current NCCN members hold NCI comprehensive designation, ensuring they adhere to rigorous federal benchmarks for transdisciplinary research, clinical services, and community outreach in and treatment. This selective process emphasizes institutions with proven track records in collaborative advancements. As of 2025, the NCCN comprises 33 , embodying the nation's premier expertise and facilitating nationwide standards for cancer management. Benefits of membership include active involvement in developing evidence-based guidelines, participation in annual conferences, and collaboration on research initiatives that influence global cancer care protocols. These opportunities enable members to share , standardize treatments, and drive improvements in outcomes across diverse populations.

Current List

The National Comprehensive Cancer Network consists of 33 leading cancer centers dedicated to advancing patient care, research, and education in oncology. As of 2025, these member institutions are distributed across the United States and are grouped below by geographic region for readability. Northeast
  • Abramson Cancer Center at the University of Pennsylvania, Philadelphia, PA
  • Dana-Farber/Brigham and Women’s Cancer Center | Mass General Cancer Center, Boston, MA
  • Fox Chase Cancer Center, Philadelphia, PA
  • Memorial Sloan Kettering Cancer Center, New York, NY
  • Roswell Park Comprehensive Cancer Center, Buffalo, NY
  • The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD
  • Yale Cancer Center/Smilow Cancer Hospital, New Haven, CT
South
  • Baptist Health Miami Cancer Institute, Miami, FL
  • Duke Cancer Institute, Durham, NC
  • Moffitt Cancer Center, Tampa, FL
  • O’Neal Comprehensive Cancer Center at UAB, Birmingham, AL
  • St. Jude Children’s Research Hospital/The University of Tennessee Health Science Center, Memphis, TN
  • The University of Texas MD Anderson Cancer Center, Houston, TX
  • UT Southwestern Simmons Comprehensive Cancer Center, Dallas, TX
  • Vanderbilt-Ingram Cancer Center, Nashville, TN
Midwest West Membership is subject to periodic review based on established criteria to ensure ongoing alignment with NCCN's mission.

Impact and Initiatives

Influence on Cancer Care

The National Comprehensive Cancer Network (NCCN) guidelines are widely adopted , with as many as 95% of oncologists using them in as of 2020 to inform decisions. These guidelines more than 97% of cancer cases diagnosed in the country, providing a comprehensive framework for evidence-based care across major tumor types. Their integration into coverage and quality metrics has standardized reimbursement and performance measures, with many payers relying on NCCN recommendations as a basis for approving treatments and off-label drug uses. Adherence to NCCN guidelines has been linked to improved patient outcomes, including higher survival rates and reduced variations in care delivery. Multiple studies demonstrate that guideline-concordant treatment correlates with better survival; for instance, nonadherence in colorectal cancer patients is associated with decreased 5-year relative survival rates (54.5% versus 67.7%). Similar findings appear in ovarian cancer, where guideline adherence improves overall survival in early-stage cases, and in soft tissue sarcomas, where it reduces mortality disparities. By promoting uniform application of best practices, NCCN efforts have minimized regional and institutional variations in treatment, leading to more equitable care across U.S. healthcare settings. NCCN exerts significant influence on U.S. cancer policy through advocacy and collaboration with federal agencies. The organization has contributed to initiatives like the National Cancer Institute's Cancer Moonshot by supporting accelerated research and policy summits that include White House coordinators, the Centers for Disease Control and Prevention, and the U.S. Preventive Services Task Force. In payer negotiations, NCCN guidelines facilitate discussions on cost-effective treatments by providing evidence-based affordability assessments and value pathways, which help insurers prioritize high-value therapies and lower total costs of care—for example, guideline adherence in colon cancer regimens has been shown to reduce spending. Through its Oncology Research Program, NCCN supports clinical trials and outcomes research at its member institutions, funding investigator-initiated studies and facilitating collaborations with pharmaceutical companies. These efforts generate from large patient cohorts, informing guideline updates and advancing precision trials that improve therapeutic options for U.S. patients. NCCN's educational initiatives play a key role in disseminating best practices to U.S. oncology professionals via annual conferences and the Journal of the National Comprehensive Cancer Network (JNCCN). The 2025 Annual Conference, marking the organization's 30th year, featured sessions on cutting-edge and multidisciplinary , attracting thousands of attendees to enhance clinical decision-making. JNCCN publishes peer-reviewed articles, guideline insights, and outcomes data, reaching over 25,000 U.S. cancer professionals as of 2020 and supporting credits for more than 140 annual activities.

Global Reach and Additional Programs

The National Comprehensive Cancer Network (NCCN) extends its influence beyond the through a dedicated Global Program, which promotes equitable cancer care worldwide by adapting guidelines, fostering collaborations, and enhancing resource accessibility. This program supports over 993,000 registered users outside the U.S. on NCCN.org and has facilitated more than 16 million global downloads of NCCN Guidelines, demonstrating widespread . NCCN collaborates with oncology organizations in regions including , , the (MENA), , , , and to tailor guidelines to local resources, practices, and regulatory environments. A key global initiative is the NCCN Framework for Resource Stratification of NCCN Guidelines (NCCN Framework™), designed specifically for low- and middle-income countries to adapt evidence-based recommendations to varying resource levels. The framework categorizes care into four progressive tiers: Basic Resources, which provide essential interventions for minimal standard care to improve survival; Core Resources, adding accessible services for significant outcome gains; Enhanced Resources, incorporating advanced options with moderate benefits or higher costs; and the full for maximal-resource settings. Developed by NCCN subcommittees with input from international clinicians, the framework ensures practical, incremental adaptations reviewed annually for relevance in resource-constrained environments. To broaden accessibility, NCCN translates its clinical guidelines into multiple languages, including , , , , , , , , , , , , and , making them freely available on NCCN.org and the NCCN mobile app. These translations, prepared by medical interpreters, support clinicians in diverse regions and have been integrated into regional adaptations, such as harmonized guidelines for developed in partnership with the African Cancer Coalition. NCCN's Policy and Advocacy Program addresses global challenges by prioritizing equity and access, collaborating with international stakeholders to reduce disparities in , treatment, and supportive care. The program hosts a tri-annual Summit Series, convening clinicians, patients, policymakers, and advocates to discuss priorities like equitable resource distribution and policy reforms for underserved populations worldwide. Through initiatives like Advancing Cancer Equity, NCCN works to dismantle systemic barriers, partnering with organizations such as the Cancer Action Network and the National Medical Association Quality Forum in the Alliance for Cancer Care Equity to advocate for inclusive policies. Complementing these efforts, the NCCN Foundation, a 501(c)(3) nonprofit established by NCCN, funds patient-centered resources such as the NCCN Guidelines for Patients—translated into languages like , , , , , , , , , , , , and —to empower individuals globally with evidence-based information. The also supports innovation and education through , including Young Investigator Awards, and relies on donations to sustain free access to these tools in low-resource settings. Additionally, NCCN partners with international entities for global education and research, such as collaborations with Medlive in for guideline dissemination and the Global Learning Collaborative for digital targeting clinicians in underserved areas.

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