Toward a standard pathological and molecular characterization of recurrent glioma in adults: a Response Assessment in Neuro-Oncology effort

Author:

Haider Ali S1,van den Bent Martin2,Wen Patrick Y3,Vogelbaum Michael A4,Chang Susan5,Canoll Peter D6,Horbinski Craig M78,Huse Jason T910

Affiliation:

1. Departments of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

2. Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands

3. Center for Neuro-Oncology, Dana-Farber/Brigham and Women’s Cancer Center and Harvard Medical School, Boston, Massachusetts, USA

4. Departments of Neurosurgery and Neuro-Oncology, Moffitt Cancer Center, Tampa, Florida, USA

5. Department of Neurological Surgery, University of California San Francisco, San Francisco, California, USA

6. Departments of Pathology and Cell Biology, Columbia University Medical Center, New York, New York, USA

7. Departments of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

8. Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

9. Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

10. Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

Abstract

Abstract Regardless of subtype, diffuse gliomas of adulthood are characterized by inexorable progression through treatment. Cancer recurrence in the context of therapy is by no means unique to gliomas. For many tumors residing outside the central nervous system (CNS), tissue-based analyses are routinely employed to document the molecular and cellular features of disease recurrence. Such interventions are inconsistently applied for gliomas, however, and lack rigorous standardization when they are. While many of the reasons underlying these discrepancies reflect pragmatic realities inherent to CNS disease, the suboptimal employment of histological and molecular assessment at recurrence nevertheless represents a missed opportunity to proactively guide patient management and increase knowledge. Herein, we address this quandary by pairing a succinct description of the histological, biological, and molecular characteristics of recurrent glioma with recommendations for how to better standardize and implement quality pathological assessment into patient management. We hope this review will prompt thoughtful revision of standard operating procedures to maximize the utility of glioma re-biopsy.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Clinical Neurology,Oncology

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