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Erschienen in: Journal of Neuro-Oncology 2/2019

16.11.2018 | Clinical Study

Histopathologic quantification of viable tumor versus treatment effect in surgically resected recurrent glioblastoma

verfasst von: Stephen J. Bagley, Robert D. Schwab, Ernest Nelson, Angela N. Viaene, Zev A. Binder, Robert A. Lustig, Donald M. O’Rourke, Steven Brem, Arati S. Desai, MacLean P. Nasrallah

Erschienen in: Journal of Neuro-Oncology | Ausgabe 2/2019

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Abstract

Purpose

The prognostic impact of the histopathologic features of recurrent glioblastoma surgical specimens is unknown. We sought to determine whether key histopathologic characteristics in glioblastoma tumors resected after chemoradiotherapy are associated with overall survival (OS).

Methods

The following characteristics were quantified in recurrent glioblastoma specimens at our institution: extent of viable tumor (accounting for % of specimen comprised of tumor and tumor cellularity), mitoses per 10 high-power fields (0, 1–10, > 10), Ki-67 proliferative index (0–100%), hyalinization (0–6; none to extensive), rarefaction (0–6), hemosiderin (0–6), and % of specimen comprised of geographic necrosis (0–100%; converted to 0–6 scale). Variables associated with OS in univariate analysis, as well as age, eastern cooperative oncology group performance status (ECOG PS), extent of repeat resection, time from initial diagnosis to repeat surgery, and O6-methylguanine-DNA methyltransferase promoter methylation, were included in a multivariable Cox proportional hazards model.

Results

37 specimens were assessed. In a multivariate model, high Ki-67 proliferative index was the only histopathologic characteristic associated with worse OS following repeat surgery for glioblastoma (hazard ratio (HR) 1.3, 95% CI 1.1–1.5, p = 0.003). Shorter time interval from initial diagnosis to repeat surgery (HR 1.11, 95% CI 1.02–1.21, p = 0.016) and ECOG PS ≥ 2 (HR 4.19, 95% CI 1.72–10.21, p = 0.002) were also independently associated with inferior OS.

Conclusion

In patients with glioblastoma undergoing repeat resection following chemoradiotherapy, high Ki-67 index in the recurrent specimen, short time to recurrence, and poor PS are independently associated with worse OS. Histopathologic quantification of viable tumor versus therapy-related changes has limited prognostic influence.
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Metadaten
Titel
Histopathologic quantification of viable tumor versus treatment effect in surgically resected recurrent glioblastoma
verfasst von
Stephen J. Bagley
Robert D. Schwab
Ernest Nelson
Angela N. Viaene
Zev A. Binder
Robert A. Lustig
Donald M. O’Rourke
Steven Brem
Arati S. Desai
MacLean P. Nasrallah
Publikationsdatum
16.11.2018
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 2/2019
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-018-03050-6

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