The T1/T2 Ratio is Associated With Resectability in Patients With Isocitrate Dehydrogenase–Mutant Astrocytomas Central Nervous System World Health Organization Grades 2 and 3

Author:

Weller Jonathan1ORCID,de Dios Eddie23,Katzendobler Sophie1,Corell Alba45,Dénes Anna45,Schmutzer-Sondergeld Michael1,Javanmardi Niloufar5,Thon Niklas16,Tonn Joerg-Christian16,Jakola Asgeir S.45ORCID

Affiliation:

1. Department of Neurosurgery, LMU University Hospital, LMU Munich, München, Germany;

2. Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg, Sweden;

3. Department of Radiology, Sahlgrenska University Hospital, Gothenburg, Sweden;

4. Department of Neurosurgery, Sahlgrenska University Hospital, Gothenburg, Sweden;

5. Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg, Sweden;

6. German Consortium for Translational Cancer Research (DKTK), Partner site Munich, Heidelberg, Germany

Abstract

BACKGROUND AND OBJECTIVES: Isocitrate dehydrogenase (IDH)–mutant astrocytomas central nervous system World Health Organization grade 2 and 3 show heterogeneous appearance on MRI. In the premolecular era, the discrepancy between T1 hypointense and T2 hyperintense tumor volume in absolute values has been proposed as a marker for diffuse tumor growth. We set out to investigate if a ratio of T1 to T2 tumor volume (T1/T2 ratio) is associated with resectability and overall survival (OS) in patients with IDH-mutant astrocytomas. METHODS: Patient data from 2 centers (Sahlgrenska University Hospital, Center A; LMU University Hospital, Center B) were collected retrospectively. Inclusion criteria were as follows: pre and postoperative MRI scans available for volumetric analysis (I), diagnosis of an IDH-mutant astrocytoma between 2003 and 2021 (II), and tumor resection at initial diagnosis (III). Tumor volumes were manually segmented. The T1/T2 ratio was calculated and correlated with extent of resection, residual T2 tumor volume, and OS. RESULTS: The study comprised 134 patients with 65 patients included from Center A and 69 patients from Center B. The median OS was 134 months and did not differ between the cohorts (P = .29). Overall, the median T1/T2 ratio was 0.79 (range 0.15-1.0). Tumors displaying a T1/T2 ratio of 0.33 or lower showed significantly larger residual tumor volumes postoperatively (median 17.9 cm3 vs 4.6 cm3, P = .03). The median extent of resection in these patients was 65% vs 90% (P = .03). The ratio itself did not correlate with OS. In multivariable analyses, larger postoperative tumor volumes were associated with shorter survival times (hazard ratio 1.02, 95% CI 1.01-1.03, P < .01). CONCLUSION: The T1/T2 ratio might be a good indicator for diffuse tumor growth on MRI and is associated with resectability in patients with IDH-mutant astrocytoma. This ratio might aid to identify patients in which an oncologically relevant tumor volume reduction cannot be safely achieved.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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