Response assessment in pediatric craniopharyngioma: recommendations from the Response Assessment in Pediatric Neuro-Oncology (RAPNO) Working Group.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
14 02 2023
Historique:
pubmed: 21 9 2022
medline: 16 2 2023
entrez: 20 9 2022
Statut: ppublish

Résumé

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

Sections du résumé

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.

Identifiants

pubmed: 36124689
pii: 6702540
doi: 10.1093/neuonc/noac221
pmc: PMC9925711
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

224-233

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Lindsey M Hoffman (LM)

Center for Cancer and Blood Disorders, Phoenix Children's Hospital, Phoenix, Arizona, USA.

Camilo Jaimes (C)

Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Kshitij Mankad (K)

Department of Radiology, Great Ormond Street Hospital for Children, London, UK.

David M Mirsky (DM)

Department of Radiology, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.

Benita Tamrazi (B)

Department of Radiology, Children's Hospital Los Angeles, Los Angeles, California, USA.

Christopher L Tinkle (CL)

Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Cassie Kline (C)

Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Aparna Ramasubramanian (A)

Department of Ophthalmology, Phoenix Children's Hospital, Phoenix, Arizona, USA.

Fatema Malbari (F)

Division of Neurology and Developmental Neurosciences, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.

Ross Mangum (R)

Center for Cancer and Blood Disorders, Phoenix Children's Hospital, Phoenix, Arizona, USA.

Holly Lindsay (H)

Division of Hematology-Oncology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.

Vincent Horne (V)

Division of Pediatric Diabetes and Endocrinology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.

David J Daniels (DJ)

Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.

Sameer Keole (S)

Department of Radiation Oncology, Mayo Clinic, Phoenix, Arizona, USA.

David R Grosshans (DR)

Department of Radiation Oncology, MD Anderson Cancer Center, Houston, Texas, USA.

Tina Young Poussaint (T)

Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Roger Packer (R)

Center for Neuroscience and Behavioral Medicine, Brain Tumor Institute, Washington, District of Columbia, USA.

Sergio Cavalheiro (S)

Pediatric Oncology Institute, Federal University of São Paulo, São Paulo, Brazil.

Brigitte Bison (B)

Diagnostic and Interventional Neuroradiology, Faculty of Medicine, University Hospital Augsburg, Augsburg, Germany.

Todd C Hankinson (TC)

Department of Neurosurgery, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, CO, USA.

Hermann L Müller (HL)

Department of Pediatrics and Pediatric Hematology/Oncology, University Children's Hospital, Klinikum Oldenburg AöR, Carl von Ossietzky University Oldenburg, 26133 Oldenburg, Germany.

Ute Bartels (U)

Department of Pediatrics, Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada.

Katherine E Warren (KE)

Division of Pediatric Neuro-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Murali Chintagumpala (M)

Division of Hematology-Oncology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.

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