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Coulter, Donald W.

0000-0002-7829-0971

Mayo Clinic

Fred and Pamela Buffett Cancer Center

Citations 2

Pediatric Hodgkin Lymphoma, Version 3.2021
Hiniker, Susan M. , Benya, Ellen C. , Bobbey, Adam J. , Cooper, Stacy , Cuglievan, Branko , Isenalumhe, Leidy , Kelly, Kara M. , Kersun, Leslie S. , Lamble, Adam J. , Larrier, Nicole, Magee, J.Fergall, Oduro, Kwadwo A. , Pacheco, Martha, Roberts, Kenneth B. , Smith, Christine M. , Sohani, Aliyah R. , Trovillion, Erin , Walling, Emily , Burns, Jennifer L. , Campbell, Mallory, Smith, Christine M , Flerlage, Jamie E. , Armenian, Saro H. , Chang, Vivian Y. , Coulter, Donald W. , Hoppe, Bradford S. , Magee, Jeffrey, Price, Anita P. , Xavier, Ana C

Journal of the National Comprehensive Cancer Network | November 24, 2021 | Volume: 19 | Issue: 6 | Pages: 733-754

10.6004/jnccn.2021.0027 Get It

Hodgkin lymphoma (HL) is a highly curable form of cancer, and current treatment regimens are focused on improving treatment efficacy while decreasing the risk of late effects of treatment. The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for pediatric HL provide recommendations on the workup, diagnostic evaluation, and treatment of classic HL, including principles of pathology, imaging, staging, systemic therapy, and radiation therapy. This portion of the NCCN Guidelines focuses on the management of pediatric classic HL in the upfront and relapsed/refractory settings.
Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
Jacobsen, Eric D. , Baiocchi, Robert A. , Buhtoiarov, Ilia N. , Butler, Erin , Goodman, Aaron M. , Gratzinger, Dita , Higman, Meghan A., Hogarty, Michael D. , Jankú, Filip , Raldow, Anne C., Stefanovic, Alexandra, Tantravahi, Srinivas K. , Walkovich, Kelly, Bergman, Mary Anne, Darlow, Susan, Go, Ronald S. , Butler, Erin B. , Campbell, Patrick , Coulter, Donald W. , Diamond, Eli L. , Flagg, Aron , Goyal, Gaurav , Hendrie, Paul C. , Karmali, Reem , Morgan, David , Raldow, Ann C. , Zhang, Ling

Journal of the National Comprehensive Cancer Network | November 15, 2021 | Volume: 19 | Issue: 11 | Pages: 1277-1303

10.6004/jnccn.2021.0053 Get It

Histiocytic neoplasms are rare hematologic disorders accounting for less than 1% of cancers of the soft tissue and lymph nodes. Clinical presentation and prognosis of these disorders can be highly variable, leading to challenges for diagnosis and optimal management of these patients. Treatment often consists of systemic therapy, and recent studies support use of targeted therapies for patients with these disorders. Observation (“watch and wait”) may be sufficient for select patients with mild disease. These NCCN Guidelines for Histiocytic Neoplasms include recommendations for diagnosis and treatment of adults with the most common histiocytic disorders: Langerhans cell histiocytosis, Erdheim-Chester disease, and Rosai-Dorfman disease.