Is Intraoperative Pathology Needed if 5-Aminolevulinic-Acid-Induced Tissue Fluorescence Is Found in Stereotactic Brain Tumor Biopsy?


Journal

Neurosurgery
ISSN: 1524-4040
Titre abrégé: Neurosurgery
Pays: United States
ID NLM: 7802914

Informations de publication

Date de publication:
01 03 2020
Historique:
received: 19 06 2018
accepted: 05 12 2018
pubmed: 3 5 2019
medline: 5 9 2020
entrez: 4 5 2019
Statut: ppublish

Résumé

Intraoperative histopathology and acquisition of multiple tissue samples in stereotactic biopsies results in a prolonged length of surgery and potentially increased complication rate. To investigate the clinical benefits of a novel strategy for stereotactic brain tumor biopsies with the assistance of 5-aminolevulinic acid (5-ALA) induced fluorescence. Patients that received 5-ALA prior to stereotactic biopsy of a suspected brain tumor were included. According to our strategy, the procedure was terminated in the case of strong fluorescence of the biopsy samples. In contrast, intraoperative histology was demanded in the case of vague/no fluorescence. Length of surgery, number of biopsy samples, diagnostic rate, and periprocedural complications were compared between these 2 groups. Altogether, 79 patients were included, and strong fluorescence was present in 62 cases (79%), vague fluorescence was in 4 cases (5%), and no fluorescence was in 13 cases (16%). The diagnostic rate was comparable in biopsies with strong fluorescence without intraoperative histopathology and cases with vague/no fluorescence with intraoperative histopathology (98% vs 100%; P = 1.000). A significantly shorter length of surgery (41 vs 77 min; P < .001) and reduced average number of biopsy samples (3.6 vs 4.9; P = .011) was found in patients with strong compared to vague/no fluorescence. However, no statically significant difference in periprocedural complications between cases with strong and vague/no fluorescence was found (7% vs 18%; P = .166). Our data demonstrate the clinical benefits of a novel strategy for stereotactic brain tumor biopsies with assistance of 5-ALA. Thus, this biopsy strategy will increase the efficiency of this standard neurosurgical procedure in the future.

Sections du résumé

BACKGROUND
Intraoperative histopathology and acquisition of multiple tissue samples in stereotactic biopsies results in a prolonged length of surgery and potentially increased complication rate.
OBJECTIVE
To investigate the clinical benefits of a novel strategy for stereotactic brain tumor biopsies with the assistance of 5-aminolevulinic acid (5-ALA) induced fluorescence.
METHODS
Patients that received 5-ALA prior to stereotactic biopsy of a suspected brain tumor were included. According to our strategy, the procedure was terminated in the case of strong fluorescence of the biopsy samples. In contrast, intraoperative histology was demanded in the case of vague/no fluorescence. Length of surgery, number of biopsy samples, diagnostic rate, and periprocedural complications were compared between these 2 groups.
RESULTS
Altogether, 79 patients were included, and strong fluorescence was present in 62 cases (79%), vague fluorescence was in 4 cases (5%), and no fluorescence was in 13 cases (16%). The diagnostic rate was comparable in biopsies with strong fluorescence without intraoperative histopathology and cases with vague/no fluorescence with intraoperative histopathology (98% vs 100%; P = 1.000). A significantly shorter length of surgery (41 vs 77 min; P < .001) and reduced average number of biopsy samples (3.6 vs 4.9; P = .011) was found in patients with strong compared to vague/no fluorescence. However, no statically significant difference in periprocedural complications between cases with strong and vague/no fluorescence was found (7% vs 18%; P = .166).
CONCLUSION
Our data demonstrate the clinical benefits of a novel strategy for stereotactic brain tumor biopsies with assistance of 5-ALA. Thus, this biopsy strategy will increase the efficiency of this standard neurosurgical procedure in the future.

Identifiants

pubmed: 31049574
pii: 5485049
doi: 10.1093/neuros/nyz086
doi:

Substances chimiques

Aminolevulinic Acid 88755TAZ87

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

366-373

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 by the Congress of Neurological Surgeons.

Auteurs

Matthias Millesi (M)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Barbara Kiesel (B)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Adelheid Wöhrer (A)

Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Institute of Neurology, Medical University of Vienna, Vienna, Austria.

Petra A Mercea (PA)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Marco Bissolo (M)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Thomas Roetzer (T)

Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Institute of Neurology, Medical University of Vienna, Vienna, Austria.

Stefan Wolfsberger (S)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Julia Furtner (J)

Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.
Department of Biomedical Imaging and image-guided Therapy, Medical University of Vienna, Vienna, Austria.

Engelbert Knosp (E)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Georg Widhalm (G)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Central Nervous System Tumours Unit, Comprehensive Cancer Center, Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

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