Leveraging stimulated Raman histology-based cellularity for random forest prediction of glioblastoma recurrence.

S Sanjeev Herr (Drexel University College of Medicine, Philadelphia, PA) N Niels Olshausen (University of California, San Francisco, San Francisco, CA) J Jasleen Kaur Y Youssef Sibih (University of California, San Francisco, San Francisco, CA) V Vardhaan Ambati (University of California, San Francisco, San Francisco, CA) K Katie Scotford (University of California, San Francisco, San Francisco, CA) T Thiebaud Picart (University of California, San Francisco, San Francisco, CA) A Akhil Kondepudi (University of Michigan, Ann Arbor, MI) A Anna-Katharina Meißner (Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany) M Melike Pekmezci T Todd Hollon (University of Michigan, Ann Arbor, MI) A Albert H. Kim S Shawn L. Hervey-Jumper

Abstract

2010 Background: Glioblastoma is a universally fatal diagnosis with extent of resection being one of the most significant predictors of overall and progression-free survival. Most patients eventually experience recurrence, with sixty percent recurring along the resection cavity. Recent work leveraging Stimulated Raman histology (SRH) and artificial intelligence (AI) has approximated glioma cellularity within the infiltrative margins. It remains unknown if these estimates of glioma burden at the infiltrative margins influence glioblastoma recurrence. This study aims to evaluate a predictive model of focal recurrence in patients with glioblastoma using SRH and AI-generated cellularity scores from tissue samples taken at the resection cavity margins. Methods: A multi-center, retrospective cohort study was conducted on patients diagnosed with glioblastoma who underwent resection followed by spatial annotated tissues acquired from the resection cavity margins. Tissues were analyzed using SRH optical imaging, and histopathology analysis was performed using confocal microscopy. Tissue cellularity was measured histologically and by optical imaging. Results: Over 400 patients and 2,200 specimens were analyzed, of which a nested subset of 60 patients were selected based on selection criteria. Using preoperative and postoperative imaging, margin samples were determined to be in an area of recurrence (n=58) or nonrecurrence (n=220). Cellularity was significantly higher in the recurrent margin sample group when compared to the nonrecurrent group (p = 0.026), which was further confirmed by a pathologist-determined cellularity score (0-3) that demonstrated similar findings (p = 0.026). Results were validated across three medical centers. Six classifiers were then trained for recurrence prediction. Using nineteen of the most predictive variables, random forests (RF) performed best with an AUC of 0.848. RF screening for the minimum practical number of variables demonstrated an AUC of 0.805 using only FastGlioma, age and extent of resection as variables. Conclusions: AI-generated cellularity scores have the potential to predict focal recurrence of glioblastoma, allowing for more tailored approaches to surgical resection and radiotherapy to increase progression-free survival.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 2010-2010
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

S

Sanjeev Herr

Drexel University College of Medicine, Philadelphia, PA

N

Niels Olshausen

University of California, San Francisco, San Francisco, CA

J

Jasleen Kaur

Y

Youssef Sibih

University of California, San Francisco, San Francisco, CA

V

Vardhaan Ambati

University of California, San Francisco, San Francisco, CA

K

Katie Scotford

University of California, San Francisco, San Francisco, CA

T

Thiebaud Picart

University of California, San Francisco, San Francisco, CA

A

Akhil Kondepudi

University of Michigan, Ann Arbor, MI

A

Anna-Katharina Meißner

Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany

M

Melike Pekmezci

T

Todd Hollon

University of Michigan, Ann Arbor, MI

A

Albert H. Kim

S

Shawn L. Hervey-Jumper