The impact of histopathology and NAB2-STAT6 fusion subtype in classification and grading of meningeal solitary fibrous tumor/hemangiopericytoma.


Journal

Acta neuropathologica
ISSN: 1432-0533
Titre abrégé: Acta Neuropathol
Pays: Germany
ID NLM: 0412041

Informations de publication

Date de publication:
02 2019
Historique:
received: 15 10 2018
accepted: 17 12 2018
revised: 04 12 2018
pubmed: 26 12 2018
medline: 28 3 2020
entrez: 26 12 2018
Statut: ppublish

Résumé

Meningeal solitary fibrous tumor (SFT)/hemangiopericytoma (HPC) is a rare tumor with propensity for recurrence and metastasis. Although multiple classification schemes have been proposed, optimal risk stratification remains unclear, and the prognostic impact of fusion status is uncertain. We compared the 2016 WHO CNS tumor grading scheme (CNS-G), a three-tier system based on histopathologic phenotype and mitotic count, to the 2013 WHO soft-tissue counterpart (ST-G), a two-tier system based on mitotic count alone, in a cohort of 133 patients [59 female, 74 male; mean age 54 years (range 20-87)] with meningeal SFT/HPC. Tumors were pathologically confirmed through review of the first tumor resection (n = 97), local recurrence (n = 35), or distant metastasis (n = 1). A STAT6 immunostain showed nuclear expression in 132 cases. NAB2-STAT6 fusion was detected in 99 of 111 successfully tested tumors (89%) including the single STAT6 immunonegative tumor. Tumors were classified by CNS-G as grade 1 (n = 43), 2 (n = 41), or 3 (n = 49), and by ST-G as SFT (n = 84) or malignant SFT (n = 49). Necrosis was present in 16 cases (12%). On follow-up, 42 patients had at least one subsequent recurrence or metastasis (7 metastasis only, 33 recurrence only, 2 patients had both). Twenty-nine patients died. On univariate analysis, necrosis (p = 0.002), CNS-G (p = 0.01), and ST-G (p = 0.004) were associated with recurrence-free (RFS) but not overall survival (OS). NAB2-STAT6 fusion type was not significantly associated with RFS or OS, but was associated with phenotype. A modified ST-G incorporating necrosis showed higher correlation with RFS (p = 0.0006) and remained significant (p = 0.02) when considering only the primary tumors. From our data, mitotic rate and necrosis appear to stratify this family of tumors most accurately and could be incorporated in a future grading scheme.

Identifiants

pubmed: 30584643
doi: 10.1007/s00401-018-1952-6
pii: 10.1007/s00401-018-1952-6
pmc: PMC6513906
doi:

Substances chimiques

NAB2 protein, human 0
Repressor Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

307-319

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Auteurs

Karen Fritchie (K)

Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA. Fritchie.Karen@Mayo.edu.

Kassandra Jensch (K)

Institute of Pathology, University Hospital Erlangen, Erlangen, Germany.

Evgeny A Moskalev (EA)

Institute of Pathology, University Hospital Erlangen, Erlangen, Germany.

Alissa Caron (A)

Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.

Sarah Jenkins (S)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.

Michael Link (M)

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

Paul D Brown (PD)

Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.

Fausto J Rodriguez (FJ)

Department of Pathology, Johns Hopkins, Baltimore, MD, USA.

Andrew Guajardo (A)

Department of Pathology, Johns Hopkins, Baltimore, MD, USA.

Daniel Brat (D)

Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

José E Velázquez Vega (JE)

Department of Pathology, Children's Healthcare of Atlanta, Atlanta, GA, USA.

Arie Perry (A)

Department of Pathology, University of California, San Francisco, CA, USA.

Ashley Wu (A)

Department of Pathology, University of California, San Francisco, CA, USA.

David R Raleigh (DR)

Department of Radiation Oncology, University of California, San Francisco, CA, USA.
Department of Neurological Surgery, University of California, San Francisco, CA, USA.

Sandro Santagata (S)

Department of Pathology, Brigham and Women's Hospital, Boston, MA, USA.

David N Louis (DN)

Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Priscilla K Brastianos (PK)

Department of Hematology/Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Alexander Kaplan (A)

Department of Neuro-oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Brian M Alexander (BM)

Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Sabrina Rossi (S)

Department of Pathology and Molecular Genetics, Ospedale Ca'Foncello, Treviso, Italy.

Fabio Ferrarese (F)

Department of Radiation Oncology, Ospedale Ca'Foncello, Treviso, Italy.

Florian Haller (F)

Institute of Pathology, University Hospital Erlangen, Erlangen, Germany.

Caterina Giannini (C)

Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.

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Classifications MeSH