Volumetric analysis of IDH-mutant lower-grade glioma: a natural history study of tumor growth rates before and after treatment.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
18 12 2020
Historique:
pubmed: 25 4 2020
medline: 27 4 2021
entrez: 25 4 2020
Statut: ppublish

Résumé

Lower-grade gliomas (LGGs) with isocitrate dehydrogenase 1 and/or 2 (IDH1/2) mutations have long survival times, making evaluation of treatment efficacy difficult. We investigated the volumetric growth rate of IDH mutant gliomas before and after treatment with established glioma therapies to determine whether a significant change in growth rate could be documented and perhaps be used in the future to evaluate treatment response to investigational agents in LGG trials. In this multicenter retrospective study, 230 adult patients with IDH1/2 mutated LGGs (World Health Organization grade II or III) undergoing surgery, radiation, or chemotherapy for progressive non-enhancing tumor were identified. Subjects were required to have 3 MRI scans containing T2/fluid attenuated inversion recovery imaging spanning a minimum of 6 months prior to treatment. A mixed-effect model was used to estimate tumor growth prior to treatment. A subset of 95 patients who received chemotherapy, radiotherapy, or chemoradiotherapy and had 2 posttreatment imaging time points available were evaluated for change in pre- and posttreatment volumetric growth rates using a piecewise mixed model. The pretreatment volumetric growth rate across all 230 patients was 27.37%/180 days (95% CI: [23.36%, 31.51%]). In the 95 patients with both pre- and posttreatment scans available, there was a significant difference in volumetric growth rates before (26.63%/180 days, 95% CI: [19.31%, 34.40%]) and after treatment (-15.24% /180 days, 95% CI: [-21.37%, -8.62%]) (P < 0.0001). The growth rates for patient subgroup with 1p/19q codeletion (N = 118) was significantly slower than the rate of the 1p/19q non-codeleted group (N = 68) (22.84% vs 35.49%, P = 0.0108). In this study, we evaluated the growth rates of IDH mutant gliomas before and after standard therapy. Further study is needed to establish whether a change in growth rate is associated with patient survival and its use as a surrogate endpoint in clinical trials for IDH mutant LGGs.

Sections du résumé

BACKGROUND
Lower-grade gliomas (LGGs) with isocitrate dehydrogenase 1 and/or 2 (IDH1/2) mutations have long survival times, making evaluation of treatment efficacy difficult. We investigated the volumetric growth rate of IDH mutant gliomas before and after treatment with established glioma therapies to determine whether a significant change in growth rate could be documented and perhaps be used in the future to evaluate treatment response to investigational agents in LGG trials.
METHODS
In this multicenter retrospective study, 230 adult patients with IDH1/2 mutated LGGs (World Health Organization grade II or III) undergoing surgery, radiation, or chemotherapy for progressive non-enhancing tumor were identified. Subjects were required to have 3 MRI scans containing T2/fluid attenuated inversion recovery imaging spanning a minimum of 6 months prior to treatment. A mixed-effect model was used to estimate tumor growth prior to treatment. A subset of 95 patients who received chemotherapy, radiotherapy, or chemoradiotherapy and had 2 posttreatment imaging time points available were evaluated for change in pre- and posttreatment volumetric growth rates using a piecewise mixed model.
RESULTS
The pretreatment volumetric growth rate across all 230 patients was 27.37%/180 days (95% CI: [23.36%, 31.51%]). In the 95 patients with both pre- and posttreatment scans available, there was a significant difference in volumetric growth rates before (26.63%/180 days, 95% CI: [19.31%, 34.40%]) and after treatment (-15.24% /180 days, 95% CI: [-21.37%, -8.62%]) (P < 0.0001). The growth rates for patient subgroup with 1p/19q codeletion (N = 118) was significantly slower than the rate of the 1p/19q non-codeleted group (N = 68) (22.84% vs 35.49%, P = 0.0108).
CONCLUSION
In this study, we evaluated the growth rates of IDH mutant gliomas before and after standard therapy. Further study is needed to establish whether a change in growth rate is associated with patient survival and its use as a surrogate endpoint in clinical trials for IDH mutant LGGs.

Identifiants

pubmed: 32328652
pii: 5824395
doi: 10.1093/neuonc/noaa105
pmc: PMC7746936
doi:

Substances chimiques

Isocitrate Dehydrogenase EC 1.1.1.41

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1822-1830

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014236
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA211015
Pays : United States
Organisme : NINDS NIH HHS
ID : R35 NS105109
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Raymond Y Huang (RY)

Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts.

Robert J Young (RJ)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.

Benjamin M Ellingson (BM)

UCLA Brain Tumor Imaging Laboratory, Center for Computer Vision and Imaging Biomarkers, Department of Radiological Sciences, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

Harini Veeraraghavan (H)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York.

Wei Wang (W)

Departments of Medicine and Neurology, Brigham and Women's Hospital, Boston, Massachusetts.

Florent Tixier (F)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York.

Hyemin Um (H)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York.

Rasheed Nawaz (R)

Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts.

Tracy Luks (T)

Department of Radiology, University of California San Francisco, San Francisco, California.

John Kim (J)

Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan.

Elizabeth R Gerstner (ER)

Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts.

David Schiff (D)

Departments of Neurology, Neurological Surgery, and Medicine, University of Virginia, Charlottesville, Virginia.

Katherine B Peters (KB)

Department of Neurology and Neurosurgery, Preston Robert Tisch Brain Tumor Center, Duke University, Durham, North Carolina.

Ingo K Mellinghoff (IK)

Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, New York.

Susan M Chang (SM)

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

Timothy F Cloughesy (TF)

Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.

Patrick Y Wen (PY)

Center for Neuro-Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.

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Classifications MeSH