NCCN Announces New Guidelines for Adolescent and Young Adult (AYA) Oncology
Written by C. Lyn Fitzgerald and reproduced with permission of NCCN. Contact at Email: [email protected], telephone: 215-690-0226.
FORT WASHINGTON, PA - The National Comprehensive Cancer Network® (NCCN®) announces that it has issued new NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Adolescent and Young Adult (AYA) Oncology. AYA patients are defined in the guidelines as individuals 15 to 39 years of age at initial cancer diagnosis. The guidelines address the critical issues that AYA patients with cancer and their caregivers encounter at diagnosis, during treatment, and after therapy.
According to the American Cancer Society's Cancer Journal for Clinicians, remarkable progress has been made in the treatment of children under the age of 15 and in adults over 40 years of age in the last 35 years, but there has been minimal improvement in the survival rate in the 70,000 new AYA patients with invasive cancer diagnosed yearly.
"There is an urgent need for increased awareness of the many unique issues responsible for these poor outcomes in the AYA oncology patients," Peter F. Coccia, MD, of the UNMC Eppley Cancer Center at The Nebraska Medical Center, chair of the NCCN AYA Oncology Panel and a member of the NCCN Board of Directors noted. "Patients in this age group with pediatric types of cancers such as acute lymphoblastic leukemia and bone and soft tissue sarcomas have better outcomes when treated with aggressive therapies utilized by pediatric oncologists. We also see worse outcomes for AYA patients diagnosed with adult onset cancers such as breast and colon cancer. We hope and believe that the new NCCN Guidelines® for AYA Oncology will make a difference in how these patients are managed throughout the course of their disease."
The NCCN Guidelines address the many factors responsible for the disappointing results in the AYA patients. In the United States, only about 10% of 15 - 19 year old patients and 1 - 2% of 20 - 39 year old patients enroll in clinical trials. Conversely, more than 90% of children under 15 years of age are managed in centers that participate in the Children's Oncology Group (COG) protocols or clinical trials. In addition, AYA patients more often lack adequate health insurance, and may not have access to either routine health care, which leads to earlier diagnosis, or to state-of-the-art care once diagnosed. Moreover, AYA patients tend to be less compliant with their prescribed treatments.
The NCCN Guidelines Panel, made up of experts in AYA oncology from the 21 NCCN Member Institutions, strongly advises that AYA patients be referred to cancer centers with expertise and experience in treating patients in this age group and the cancers that affect them. They cite improved enrollment in clinical trials, the need for a multidisciplinary approach to treatment, and specific attention to the special physical and psychosocial issues that AYA patients face as critical components in delivering state-of-the-art care.
The NCCN Guidelines include recommendations for fertility preservation; screening recommendations for late effects after successful completion of therapy; palliative care and end-of- life considerations for patients who fail curative therapy; and detail the available on-line resources for AYA patients and cancer survivors.
Bradley J. Zebrack, Ph.D., M.S.W., M.P.H., of the University of Michigan Rogel Cancer Center, a member of the NCCN AYA Oncology Panel, stresses the importance of understanding and managing psychosocial issues for these patients.
"Psychological distress is significantly greater among AYA patients as compared to younger children or older patients with cancer. These patients face serious problems related to loss of fertility, disruptions in their education or their careers, and their social interactions -- in addition to the threat to their mortality. These issues, and the isolation that accompanies them, can affect their lives for many years. Managing these patients medically and communicating effectively with them can be challenging, and requires that the full team of health care providers be knowledgeable about adolescent behavior. The team must also be well trained in how to communicate with teens and young adults, as well as their families and peers. The new NCCN Guidelines include a comprehensive psychosocial assessment to assure that these issues are fully addressed."
The NCCN Guidelines for AYA Oncology will be presented next week at the NCCN 17th Annual Conference: Clinical Practice Guidelines & Quality Cancer Care™.
The NCCN Guidelines are developed and updated through an evidence-based process in which the expert panel integrates comprehensive clinical and scientific data with the judgment of the multidisciplinary panel members and other experts drawn from NCCN Member Institutions. Access to the NCCN Guidelines for AYA Oncology or any of the NCCN Guidelines is available free of charge at NCCN.org.
About the National Comprehensive Cancer Network
The National Comprehensive Cancer Network® (NCCN®), a not-for-profit alliance of 26 of the world's leading cancer centers, is dedicated to improving the quality and effectiveness of care provided to patients with cancer. Through the leadership and expertise of clinical professionals at NCCN Member Institutions, NCCN develops resources that present valuable information to the numerous stakeholders in the health care delivery system. As the arbiter of high-quality cancer care, NCCN promotes the importance of continuous quality improvement and recognizes the significance of creating clinical practice guidelines appropriate for use by patients, clinicians, and other health care decision-makers. The primary goal of all NCCN initiatives is to improve the quality, effectiveness, and efficiency of oncology practice so patients can live better lives.