Is IDH status the only factor predicting prognosis in newly diagnosed anaplastic glioma patients? Outcome evaluation and prognostic factor analysis in a single-institution large series.

anaplastic glioma chemotherapy oncology prognostic factors radiation therapy surgery

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
04 Sep 2020
Historique:
received: 06 04 2020
accepted: 21 05 2020
medline: 5 9 2020
pubmed: 5 9 2020
entrez: 4 9 2020
Statut: epublish

Résumé

Anaplastic gliomas (AGs) are an extremely heterogeneous group of primary brain tumors. More recently, new discoveries have indicated that isocitrate dehydrogenase (IDH) mutation status is the most important parameter predicting survival. The primary aim of the present analysis was to identify prognostic factors, other than IDH status, that eventually impact survival. Patients with available clinical, imaging, and molecular profile data who were amenable to resection were evaluated. The extent of resection (EOR) was defined as gross-total resection (GTR), near-total resection (NTR), subtotal resection (STR), or partial resection (PR). Residual tumor volume (RTV) was quantified. Following surgery, patients received adjuvant chemotherapy alone, radiation therapy plus concomitant and adjuvant temozolomide (TMZ), or sequential radio-chemotherapy. Clinical outcome was evaluated by neurological examination and MRI 1 month after treatment and every 4 months thereafter. Tumor progression was defined according to the Response Assessment in Neuro-Oncology (RANO) working group. Among 402 patients referred to the authors' institution for AG, 142 were included in the present analysis. Eighty-eight (62%) were male and 54 (38%) were female, with a median age of 43 years (range 19-70 years). At admission, most patients had a Karnofsky Performance Scale score of 90-100 (84.5%) and were symptomatic (93.7%). Forty-eight (33.8%) patients had newly diagnosed anaplastic oligodendrogliomas (AOs), and 94 (66.2%) had anaplastic astrocytomas (AAs). Most of them had mutant IDH tumors (67.6%) and methylated O 6-methylguanine-DNA-methyltransferase (MGMT) promoter status (71.8%). GTR was performed in more than half of the patients (56.3%). RTV was detected in 83 (58.5%) patients. Following surgery, 72 (50.7%) patients received radiotherapy with concomitant and adjuvant TMZ, 48 (33.8%) received sequential radio-chemotherapy, and 22 (15.5%) received adjuvant chemotherapy alone. The median follow-up time was 40 months (range 16-146 months). The median PFS time and the 1-, 3-, and 5-year PFS rates were 35 months (95% CI 27-76) and 78.9% ± 3.4%, 49.7% ± 4.6%, and 42.7% ± 5.4%, respectively. The median OS time and the 1-, 3-, and 5-year OS rates were 91 months (95% CI 66-95) and 90.1% ± 2.5%, 70.9% ± 4.2%, and 61.8% ± 4.9%, respectively. Prognostic factors predicting survival other than molecular profile were the EOR and the RTV (p < 0.0001). Sequential radio-chemotherapy was the more effective treatment administered. In addition to IDH status, EOR and the RTV have proved to statistically impact survival. The pivotal role of adjuvant radiotherapy has been recorded in all AG patients, regardless of tumor features.

Identifiants

pubmed: 32886916
doi: 10.3171/2020.5.JNS201116
pii: 2020.5.JNS201116
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

64-77

Auteurs

Pierina Navarria (P)

Departments of1Radiotherapy and Radiosurgery.

Federico Pessina (F)

2Neurosurgery.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Elena Clerici (E)

Departments of1Radiotherapy and Radiosurgery.

Davide Franceschini (D)

Departments of1Radiotherapy and Radiosurgery.

Giuseppe D'Agostino (G)

Departments of1Radiotherapy and Radiosurgery.

Ciro Franzese (C)

Departments of1Radiotherapy and Radiosurgery.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Tiziana Comito (T)

Departments of1Radiotherapy and Radiosurgery.

Mauro Loi (M)

Departments of1Radiotherapy and Radiosurgery.

Matteo Simonelli (M)

3Oncology and Hematology, and.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Elena Lorenzi (E)

3Oncology and Hematology, and.

Pasquale Persico (P)

3Oncology and Hematology, and.

Letterio Salvatore Politi (LS)

4Neuroradiology, Humanitas Cancer Center and Research Hospital, Rozzano.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Marco Grimaldi (M)

4Neuroradiology, Humanitas Cancer Center and Research Hospital, Rozzano.

Lorenzo Bello (L)

6Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, Italy.

Armando Santoro (A)

3Oncology and Hematology, and.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Maurizio Fornari (M)

2Neurosurgery.

Franco Servadei (F)

2Neurosurgery.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Marta Scorsetti (M)

Departments of1Radiotherapy and Radiosurgery.
5Department of Biomedical Sciences, Humanitas University, Rozzano; and.

Classifications MeSH