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Response assessment in pediatric craniopharyngioma: recommendations from the Response Assessment in Pediatric Neuro-Oncology (RAPNO) Working Group.
Hoffman, Lindsey M; Jaimes, Camilo; Mankad, Kshitij; Mirsky, David M; Tamrazi, Benita; Tinkle, Christopher L; Kline, Cassie; Ramasubramanian, Aparna; Malbari, Fatema; Mangum, Ross; Lindsay, Holly; Horne, Vincent; Daniels, David J; Keole, Sameer; Grosshans, David R; Young Poussaint, Tina; Packer, Roger; Cavalheiro, Sergio; Bison, Brigitte; Hankinson, Todd C; Müller, Hermann L; Bartels, Ute; Warren, Katherine E; Chintagumpala, Murali.
Afiliação
  • Hoffman LM; Center for Cancer and Blood Disorders, Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Jaimes C; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Mankad K; Department of Radiology, Great Ormond Street Hospital for Children, London, UK.
  • Mirsky DM; Department of Radiology, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Tamrazi B; Department of Radiology, Children's Hospital Los Angeles, Los Angeles, California, USA.
  • Tinkle CL; Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Kline C; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Ramasubramanian A; Department of Ophthalmology, Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Malbari F; Division of Neurology and Developmental Neurosciences, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
  • Mangum R; Center for Cancer and Blood Disorders, Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Lindsay H; Division of Hematology-Oncology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
  • Horne V; Division of Pediatric Diabetes and Endocrinology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
  • Daniels DJ; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Keole S; Department of Radiation Oncology, Mayo Clinic, Phoenix, Arizona, USA.
  • Grosshans DR; Department of Radiation Oncology, MD Anderson Cancer Center, Houston, Texas, USA.
  • Young Poussaint T; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Packer R; Center for Neuroscience and Behavioral Medicine, Brain Tumor Institute, Washington, District of Columbia, USA.
  • Cavalheiro S; Pediatric Oncology Institute, Federal University of São Paulo, São Paulo, Brazil.
  • Bison B; Diagnostic and Interventional Neuroradiology, Faculty of Medicine, University Hospital Augsburg, Augsburg, Germany.
  • Hankinson TC; Department of Neurosurgery, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, CO, USA.
  • Müller HL; Department of Pediatrics and Pediatric Hematology/Oncology, University Children's Hospital, Klinikum Oldenburg AöR, Carl von Ossietzky University Oldenburg, 26133 Oldenburg, Germany.
  • Bartels U; Department of Pediatrics, Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada.
  • Warren KE; Division of Pediatric Neuro-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Chintagumpala M; Division of Hematology-Oncology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
Neuro Oncol ; 25(2): 224-233, 2023 02 14.
Article em En | MEDLINE | ID: mdl-36124689
ABSTRACT

BACKGROUND:

Craniopharyngioma is a histologically benign tumor of the suprasellar region for which survival is excellent but quality of life is often poor secondary to functional deficits from tumor and treatment. Standard therapy consists of maximal safe resection with or without radiation therapy. Few prospective trials have been performed, and response assessment has not been standardized.

METHODS:

The Response Assessment in Pediatric Neuro-Oncology (RAPNO) committee devised consensus guidelines to assess craniopharyngioma response prospectively.

RESULTS:

Magnetic resonance imaging is the recommended radiologic modality for baseline and follow-up assessments. Radiologic response is defined by 2-dimensional measurements of both solid and cystic tumor components. In certain clinical contexts, response to solid and cystic disease may be differentially considered based on their unique natural histories and responses to treatment. Importantly, the committee incorporated functional endpoints related to neuro-endocrine and visual assessments into craniopharyngioma response definitions. In most circumstances, the cystic disease should be considered progressive only if growth is associated with acute, new-onset or progressive functional impairment.

CONCLUSIONS:

Craniopharyngioma is a common pediatric central nervous system tumor for which standardized response parameters have not been defined. A RAPNO committee devised guidelines for craniopharyngioma assessment to uniformly define response in future prospective trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Craniofaringioma Tipo de estudo: Guideline Aspecto: Patient_preference Limite: Child / Humans Idioma: En Revista: Neuro Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Craniofaringioma Tipo de estudo: Guideline Aspecto: Patient_preference Limite: Child / Humans Idioma: En Revista: Neuro Oncol Ano de publicação: 2023 Tipo de documento: Article