The role of clinical and molecular factors in low-grade gliomas: what is their impact on survival?

Author:

Franceschi Enrico1,Mura Antonella1,De Biase Dario2,Tallini Giovanni3,Pession Annalisa2,Foschini Maria Pia4,Danieli Daniela5,Pizzolitto Stefano6,Zunarelli Elena7,Lanza Giovanni8,Bartolini Daniela9,Silini Enrico Maria10,Visani Michela3,Di Oto Enrico11,Tosoni Alicia1,Minichillo Santino1,Lamberti Giuseppe1,Lanese Andrea1,Paccapelo Alexandro1,Bartolini Stefania1,Brandes Alba A1

Affiliation:

1. Department of Medical Oncology, Bellaria-Maggiore Hospitals, Azienda USL, IRCCS Institute of Neurological Sciences, Bologna, Italy

2. Department of Pharmacy and Biotechnology (FaBiT), Molecular Diagnostic Unit AUSL ofBologna, University of Bologna, Bologna, Italy

3. Department of Medicine (Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale) – Molecular Diagnostic Unit, Azienda USL di Bologna, University of Bologna School of Medicine, Bologna, Italy

4. Department of Biomedical & Neuro Motor Sciences, Anatomic Pathology ‘M Malpighi’ at Bellaria Hospital, University of Bologna, Bologna, Italy

5. Department of Pathology, San Bortolo Hospital, Vicenza, Italy

6. Department of Pathology, Santa Maria della Misericordia Hospital, Udine, Italy

7. Department of Pathology, University Hospital, Modena, Italy

8. Department of Pathology, S Anna University Hospital & University of Ferrara, Ferrara, Italy

9. Department of Pathology, Bufalini Hospital, Cesena, Italy

10. Department of Pathology, University Hospital of Parma, Via Gramsci 14, 43100, Parma, Italy

11. Section of Anatomic Pathology, Department of Biomedical & Neuromotor Sciences, University of Bologna, 40139, Bologna, Italy

Abstract

Aim: To evaluate relevance of clinical and molecular factors in adult low-grade gliomas (LGG) and to correlate with survival. Methods: We reviewed records from adult LGG patients from 1991 to 2015 who received surgery and had sufficient tissue to molecular biomarkers characterization. Results: 213 consecutive LGG patients were included: 17.4% were low-risk, according to Radiation Therapy Oncology Group (RTOG) risk assessment. IDH 1/2 mutation, 1p/19q co-deletion, MGMT methylation were found in 93, 50.8 and 65.3% of patients. Median follow-up was 98.3 months. In univariate analysis, overall survival was influenced by extent of resection (p = 0.011), IDH mutation (p < 0.001), 1p/19q co-deletion (p = 0.015) and MGMT methylation (p = 0.013). In multivariate analysis, RTOG clinical risk (p = 0.006), IDH mutation (p < 0.001) and 1p/19q co-deletion (p = 0.035) correlated with overall survival. RTOG clinical risk (p = 0.006), IDH mutation (p < 0.001) and 1p/19q co-deletion (p = 0.035) correlated with overall survival. Conclusion: Both clinical and molecular factors are essential to determine prognosis and treatment strategies.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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