Evidence map›Paper›PMID 42666069›Full record

ArticleBrain pathology (Zurich, Switzerland)2026

AOSNP-ADAPTR resource level-based recommendations on practical diagnostic strategies for medulloblastomas and other embryonal tumors.

Chitra Sarkar, Maysa Al-Hussaini, Vani Santosh, Vaishali Suri, Sung-Hye Park, Yue-Shan Piao, Tarik Tihan, Ho-Keung Ng, Michael Buckland, Rakesh Jalali and 3 more

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Article in Brain pathology (Zurich, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Chitra SarkarDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.ORCID https://orcid.org/0000-0002-4315-9316
Maysa Al-HussainiDepartment of Cell Therapy and Applied Genomics, King Hussein Cancer Center, Amman, Jordan.ORCID https://orcid.org/0000-0001-6392-150X
Vani SantoshDepartment of Neuropathology, National Institute of Mental Health and Neuro Sciences, Bengaluru, India.ORCID https://orcid.org/0000-0001-8724-2034
Vaishali SuriDepartment of Neuropathology, Neurosciences Centre, All India Institute of Medical Sciences, New Delhi, India.ORCID https://orcid.org/0000-0001-6485-8194
Sung-Hye ParkDepartment of Pathology, Seoul National University, College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-8681-1597
Yue-Shan PiaoDepartment of Neuropathology, Xuanwu Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0001-6081-1129
Tarik TihanDepartment of Pathology, Neuropathology Unit, University of Miami Miller School, Miami, Florida, USA.ORCID https://orcid.org/0000-0003-4551-2555
Ho-Keung NgDepartment of Anatomical and Cellular Pathology, Chinese University of Hong Kong, Hong Kong.ORCID https://orcid.org/0000-0002-2614-2213
Michael BucklandDepartment of Neuropathology, Royal Prince Alfred Hospital, Sydney, Australia.ORCID https://orcid.org/0000-0003-4755-6471
Rakesh JalaliNeuro-Oncology Cancer Management Team, Apollo Proton Cancer Centre, Chennai, India.ORCID https://orcid.org/0000-0002-0318-5536
Yonehiro KanemuraInstitute for Clinical Research, National Hospital Organization Osaka National Hospital, Osaka, Japan.ORCID https://orcid.org/0000-0002-1894-1824
Pieter WesselingDepartment of Pathology, Amsterdam University Medical Centers/VU University, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-5453-5201
Takashi KomoriDepartment of Laboratory Medicine and Pathology, Tokyo Metropolitan Neurological Hospital, Tokyo Metropolitan Hospital Organization, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6812-2149

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

WHO CNS5 mandates integrated histo-molecular classification of medulloblastomas (MBs) and other CNS embryonal tumors. However, advanced molecular diagnostics remain inaccessible in many low- and lower-middle-income countries (LICs/LMICs), limiting implementation of molecularly informed risk stratification and therapy. The ADAPTR group (Adapting Diagnostic Approaches for Practical Taxonomy in Resource-Restrained Regions) is an initiative of the Asian Oceanian Society of Neuropathology (AOSNP) and aims to provide practical guidelines for CNS tumor diagnostics at various levels of pathology resource restraints. In this manuscript, we propose a practical approach to diagnosis of MBs and other CNS embryonal tumors based on ADAPTR resource levels (RLs). The emphasis is mainly on using histopathological approaches with immunohistochemistry (IHC), while molecular testing recommendations are categorized as "can be considered," "highly recommended" or "obligatory" to reach the next level diagnosis. In each RL, either a WHO CNS5 diagnosis with an accompanying CNS WHO grade or an ADAPTR descriptive diagnosis with an associated ADAPTR histologic grade and comment is provided, depending on the context. "Histology-oriented integrated diagnosis format" for each tumor type at different RLs along with diagnostic flow charts has been generated to suit these RLs. For MBs, at RL I-II, diagnosis relies on histopathology and basic IHC with structured ADAPTR descriptive reporting. At RL III, surrogate IHC panels enable assignment to WNT-activated, SHH-activated and non-WNT/non-SHH groups, facilitating clinically actionable risk stratification. RL IV incorporates targeted molecular tests (e.g., MYC/MYCN amplification, CTNNB1 and TP53 mutations) for prognostic refinement. RL V supports comprehensive molecular classification through next-generation sequencing and DNA methylation profiling. Parallel RL-based algorithms are proposed for other CNS embryonal tumors, incorporating essential surrogate and confirmatory markers. These AOSNP-ADAPTR recommendations provide a practical adaptation of WHO CNS5 guidelines suited to routine diagnosis in resource-restrained regions. This model promotes equitable, risk-adapted care while supporting progressive strengthening of global neuropathology capacity.

Indexed as

AOSNP‐ADAPTRimmunohistochemical markersmedulloblastomamolecular groupsother CNS embryonal tumorsresource‐restrained regions

Identifiers

PMID42666069
PMCPMC13525349

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.