Imaging growth as a predictor of grade of malignancy and aggressiveness of IDH-mutant and 1p/19q-codeleted oligodendrogliomas in adults

Author:

Roux Alexandre123,Tauziede-Espariat Arnault234,Zanello Marc123,Peeters Sophie5,Zah-Bi Gilles123,Parraga Eduardo123,Edjlali Myriam236,Lechapt Emmanuèle234,Shor Natalia7,Bellu Luisa8,Berzero Giulia8,Dormont Didier7,Dezamis Edouard123,Chretien Fabrice2349,Oppenheim Catherine236,Sanson Marc8,Varlet Pascale234,Capelle Laurent10,Dhermain Frédéric11,Pallud Johan123ORCID

Affiliation:

1. Department of Neurosurgery, University Hospital Group for Psychiatry and Neurosciences (GHU)–Sainte-Anne Hospital, Paris, France

2. Paris Descartes University, Sorbonne Paris Cité, Paris, France

3. INSERM Unit 1266, Imaging Biomarkers of Brain Disorders (IMA-BRAIN), Institute of Psychiatry and Neurosciences of Paris, Paris, France

4. Department of Neuropathology, GHU–Sainte-Anne Hospital, Paris, France

5. Department of Neurosurgery, University of California Los Angeles, Los Angeles, California, USA

6. Department of Neuroradiology, GHU–Sainte-Anne Hospital, Paris, France

7. Department of Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France

8. Department of Neuro-Oncology, Pitié-Salpêtrière Hospital, Paris, France

9. Laboratory of Experimental Neuropathology, Pasteur Institute, Paris, France

10. Department of Neurosurgery, Pitié-Salpêtrière Hospital, Paris, France

11. Department of Radiotherapy, Gustave Roussy University Hospital, Villejuif, France

Abstract

Abstract Background We quantified the spontaneous imaging growth rate of oligodendrogliomas. We assessed whether (i) it discriminates between World Health Organization (WHO) grade II and grade III oligodendrogliomas, and (ii) grade III oligodendrogliomas with neo-angiogenesis are associated with more fast growth rates (≥8 mm/y). Methods This work employed a retrospective bicentric cohort study (2010–2016) of adult patients harboring a newly diagnosed supratentorial oligodendroglioma, isocitrate dehydrogenase (IDH) mutant and 1p/19q codeleted (WHO 2016 classification), with a minimum of 2 available MRIs before any treatment (minimum 6-week interval) to measure the spontaneous tumor growth rate. Results We included 108 patients (age 44.7 ± 14.1 y, 60 males). The tumor growth rate was higher in grade III oligodendrogliomas with neo-angiogenesis (n = 37, median 10.4 mm/y, mean 10.0 ± 6.9) than in grade III oligodendrogliomas with increased mitosis count only (cutoff ≥6 mitoses, n = 18, median 3.9 mm/y, mean 4.5 ± 3.2; P = 0.004), and higher than in grade II oligodendrogliomas (n = 53, median 2.3 mm/y, mean 2.8 ± 2.2; P < 0.001). There was increased prevalence of fast tumor growth rates in grade III oligodendrogliomas with neo-angiogenesis (54.1%) compared with grade III oligodendrogliomas with increased mitosis count only (11.1%; P < 0.001), and in grade II oligodendrogliomas (0.0%; P < 0.001). The tumor growth rate trends did not differ between centers (P = 0.121). Neo-angiogenesis (P < 0.001) and mitosis count at ≥9 (P = 0.013) were independently associated with tumor growth rates ≥8 mm/year. A tumor growth rate ≥8 mm/year was the only predictor independently associated with shorter progression-free survival (P = 0.041). Conclusions The spontaneous tumor growth rate recapitulates oligodendroglioma aggressiveness, permits identification of grade III oligodendrogliomas preoperatively when ≥8 mm/year, and questions the grading by mitosis count.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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