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1.
J Natl Compr Canc Netw ; 21(9): 910-914.e1, 2023 09.
Article in English | MEDLINE | ID: mdl-37673113

ABSTRACT

Cancer prevention, screening, and early detection play an integral role in cancer incidence and outcomes. It is estimated that 30% to 50% of cancers worldwide are preventable, and it is well established that early detection of many cancers is associated with improved treatment outcomes. A recent NCCN Policy Summit: Reducing the Cancer Burden Through Prevention and Early Detection brought together healthcare providers, payers, policymakers, patient advocates, industry representatives, and technology representatives to explore challenges, triumphs, and outstanding questions surrounding current practices. Keynotes were delivered by Dr. Lisa Richardson, Director of the Division of Cancer Prevention and Control within the CDC, and Dr. Danielle Carnival, White House Cancer Moonshot Coordinator. Dr. Richardson focused on the field of public health, translating its utility in preventing and diagnosing cancer in the United States, while Dr. Carnival discussed ambitious goals by the Cancer Moonshot in reducing the cancer burden. Panelists highlighted characteristics of high-impact prevention and early detection programs, including how genetic testing has impacted this space. Existing programs are often challenged due to limitations in data, as well as financial, structural, and social barriers to motivating individuals to act on recommendations. Despite these barriers, we can learn from highly successful programs and should apply proven attributes, such as community engagement, more broadly.


Subject(s)
Genetic Testing , Neoplasms , Humans , Health Personnel , Policy , Neoplasms/diagnosis , Neoplasms/epidemiology , Neoplasms/prevention & control
2.
J Natl Compr Canc Netw ; 21(6)2023 06 12.
Article in English | MEDLINE | ID: mdl-37308116

ABSTRACT

US healthcare systems have been deeply impacted by significant societal shifts over the past several years. The COVID-19 pandemic has changed the way we interact with healthcare, political narratives have impacted how healthcare is perceived and engaged with by the public, and the United States has become increasingly aware of historic and ongoing racial injustices across all health and social systems. The watershed events experienced during the last several years play a critical role in shaping the future of cancer care for payers, providers, manufacturers, and, most importantly, patients and survivors. To explore these issues, in June 2021 NCCN convened a virtual policy summit: Defining the "New Normal" - 2021 and the State of Cancer Care in America Following 2020. This summit offered the opportunity for a varied group of stakeholders to begin to explore the impact of recent events on the current and future state of oncology in the United States. Topics included the impact of COVID-19 on cancer detection and treatment, the role of innovation in ensuring continuity of care, and efforts to create more equitable systems of care.


Subject(s)
COVID-19 , Neoplasms , Humans , Pandemics , Health Facilities , Policy
3.
J Natl Compr Canc Netw ; 21(5): 459-464, 2023 05.
Article in English | MEDLINE | ID: mdl-37156481

ABSTRACT

Survival rates for people with cancer and quality of life for survivors have increased significantly as a result of innovations in cancer treatment, improvements in early detection, and improved healthcare access. In the United States, 1 in 2 men and 1 in 3 women will be diagnosed with cancer in their lifetime. As more cancer survivors and patients remain in the workforce, employers must evaluate how they can adjust workplace policies to meet employee and business needs. Unfortunately, many people still encounter barriers to remaining in the workplace following a cancer diagnosis for themselves or a loved one. In an effort to explore the impacts of contemporary employment policies on patients with cancer, cancer survivors, and caregivers, NCCN hosted the Policy Summit "Cancer Care in the Workplace: Building a 21st Century Workplace for Cancer Patients, Survivors, and Caretakers" on June 17, 2022. This hybrid event, through keynotes and multistakeholder panel discussions, explored issues regarding employer benefit design, policy solutions, current best and promising practices for return to work, and how these issues impact treatment, survivorship, and caregiving in the cancer community.


Subject(s)
Neoplasms , Quality of Life , Male , Humans , Female , United States/epidemiology , Workplace , Employment , Survivors , Neoplasms/diagnosis , Neoplasms/epidemiology , Neoplasms/therapy , Policy
4.
J Natl Compr Canc Netw ; 21(2): 117-124.e3, 2023 02.
Article in English | MEDLINE | ID: mdl-36791757

ABSTRACT

The root causes of racial disparities in access to optimal cancer care and related cancer outcomes are complex, multifactorial, and not rooted in biology. Contributing factors to racial disparities in care delivery include implicit and explicit bias, lack of representation of people of color in the oncology care and research workforce, and homogenous research participants that are not representative of the larger community. Systemic and structural barriers include policies leading to lack of insurance and underinsurance, costs of cancer treatment and associated ancillary costs of care, disparate access to clinical trials, and social determinants of health, including exposure to environmental hazards, access to housing, childcare, and economic injustices. To address these issues, ACS CAN, NCCN, and NMQF convened the Elevating Cancer Equity (ECE) initiative. The ECE Working Group developed the Health Equity Report Card (HERC). In this manuscript, we describe the process taken by the ECE Working Group to develop the HERC recommendations, the strategies employed by NCCN to develop an implementation plan and scoring methodology for the HERC, and next steps to pilot the HERC tool in practice settings.


Subject(s)
Health Equity , Neoplasms , Humans , Delivery of Health Care , Neoplasms/epidemiology , Neoplasms/therapy , Medical Oncology , Policy , Healthcare Disparities
5.
J Natl Compr Canc Netw ; 18(9): 1181-1187, 2020 09.
Article in English | MEDLINE | ID: mdl-32886908

ABSTRACT

As the oncology ecosystem shifts from service-based care to outcomes and value-based care, stakeholders cite concerns regarding the lack of patient experience data that are important to the patient community. To address the patient perspective and highlight the challenges and opportunities within policy and clinical decision-making to improve patient-centered care, NCCN hosted the NCCN Patient Advocacy Summit: Delivering Value for Patients Across the Oncology Ecosystem on December 11, 2019, in Washington, DC. The summit featured multidisciplinary panel discussions, keynote speakers, and patient advocate presentations exploring the implications for patient-centered care within a shifting health policy landscape. This article encapsulates and expounds upon the discussions and presentations from the summit.


Subject(s)
Medical Oncology , Neoplasms , Patient Advocacy , Health Policy , Humans , Neoplasms/therapy
6.
J Natl Compr Canc Netw ; 18(7): 820-824, 2020 07.
Article in English | MEDLINE | ID: mdl-32634773

ABSTRACT

Quality measurement is a critical component of advancing a health system that pays for performance over volume. Although there has been significant attention paid to quality measurement within health systems in recent years, significant challenges to meaningful measurement of quality care outcomes remain. Defining cost can be challenging, but is arguably not as elusive as quality, which lacks standard measurement methods and units. To identify industry standards and recommendations for the future, NCCN recently hosted the NCCN Oncology Policy Summit: Defining, Measuring, and Applying Quality in an Evolving Health Policy Landscape and the Implications for Cancer Care. Key stakeholders including physicians, payers, policymakers, patient advocates, and technology partners reviewed current quality measurement programs to identify success and challenges, including the Oncology Care Model. Speakers and panelists identified gaps in quality measurement and provided insights and suggestions for further advancing quality measurement in oncology. This article provides insights and recommendations; however, the goal of this program was to highlight key issues and not to obtain consensus.


Subject(s)
Health Policy , Medical Oncology , Neoplasms , Quality of Health Care , Humans , Neoplasms/therapy
7.
J Natl Compr Canc Netw ; 18(4): 400-404, 2020 04.
Article in English | MEDLINE | ID: mdl-32259786

ABSTRACT

Health policy in America has shifted rapidly over the last decade, and states are increasingly exercising greater authority over health policy decision-making. This localization and regionalization of healthcare policy poses significant challenges for patients with cancer, providers, advocates, and policymakers. To identify the challenges and opportunities that lay ahead of stakeholders, NCCN hosted the 2019 Policy Summit: The State of Cancer Care in America on June 27, 2019, in Washington, DC. The summit featured multidisciplinary panel discussions to explore the implications for access to quality cancer care within a shifting health policy landscape from a patient, provider, and lawmaker perspective. This article encapsulates the discussion from this NCCN Policy Summit.


Subject(s)
Delivery of Health Care/statistics & numerical data , Delivery of Health Care/standards , Medical Oncology/standards , Neoplasms/epidemiology , Delivery of Health Care/trends , Health Policy , Health Services Accessibility , Humans , Medical Oncology/legislation & jurisprudence , Medical Oncology/statistics & numerical data , Medical Oncology/trends , Quality of Health Care , United States/epidemiology
8.
J Natl Compr Canc Netw ; 18(3): 250-259, 2020 03.
Article in English | MEDLINE | ID: mdl-32135508

ABSTRACT

Although oncology care has evolved, outcome assessment remains a key challenge. Outcome measurement requires identification and adoption of a succinct list of metrics indicative of high-quality cancer care for use within and across healthcare systems. NCCN established an advisory committee, the NCCN Quality and Outcomes Committee, consisting of provider experts from NCCN Member Institutions and other stakeholders, including payers and patient advocacy, community oncology, and health information technology representatives, to review the existing quality landscape and identify contemporary, relevant cancer quality and outcomes measures by reevaluating validated measures for endorsement and proposing new measure concepts to fill crucial gaps. This manuscript reports on 22 measures and concepts; 15 that align with existing measures and 7 that are new.


Subject(s)
Cancer Care Facilities/standards , Quality of Health Care/standards , Humans
9.
J Natl Compr Canc Netw ; 17(9): 1043-1048, 2019 09 01.
Article in English | MEDLINE | ID: mdl-31487682

ABSTRACT

Demographic factors such as race, socioeconomic status, gender identity, area of residence, native language, and cultural barriers have an effect on outcomes in cancer care. To identify unmet needs, challenges, and opportunities in achieving high-quality, patient-centered cancer care for all, NCCN conducted a yearlong environmental scan, which involved stakeholder meetings with patients and patient advocacy groups to discuss these topics. The findings from this scan informed the corresponding NCCN Patient Advocacy Summit: Advocating for Equity in Cancer Care, held in Washington, DC, on December 10, 2018. In addition to the many patient advocacy groups, the summit featured a number of other stakeholders that advocate for equity in cancer care. This article encapsulates the findings of the environmental scan and the discussion from the NCCN Patient Advocacy Summit.


Subject(s)
Health Equity , Neoplasms/epidemiology , Patient Advocacy , Patient Care , Ethnicity , Healthcare Disparities , Humans , Neoplasms/diagnosis , Neoplasms/therapy , Patient Care/standards , United States/epidemiology
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