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E-Poster Display

381P - Adult brainstem gliomas: Clinicopathological profile and outcomes of a single center 10-year cohort

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Central Nervous System Malignancies

Presenters

Alice Morais

Citation

Annals of Oncology (2020) 31 (suppl_4): S396-S408. 10.1016/annonc/annonc269

Authors

A.N.R. Morais1, G.T. Stock1, C.C.B.D.L. Zampieri1, V.P.D. Camargo1, R.C. Bonadio1, T.D.A.L. Freddi2, A.T.C. Chen3, R.C. Ghelfond3, O. Feher1

Author affiliations

  • 1 Medical Oncology Dept., ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR
  • 2 Radiology Dept., ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR
  • 3 Radiation Oncology Dept., ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR

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Abstract 381P

Background

Brainstem gliomas (BG) are rare entities in adults. The histopathological diagnosis is challenging, and the treatment(tmt) remains controversial, relying on scarce retrospective studies, some of which included children, whose disease generally has distinct behaviour. We aimed to describe baseline features, tto and outcomes for adult patients (pts) with BG exploring possible prognostic factors (PF).

Methods

We performed a single-center retrospective analysis of pts with BG older than 18 ys, treated between 2008-2018. Data were collected from electronic medical records, including clinical and histopathological features and outcomes. Pre-treatment MRIs were reviewed by a neuro-radiologist.

Results

24 pts were evaluated. Median age at diagnosis was 36 ys (r 22-59); 67% male. Motor deficit (50%) and headache (46%) were the most frequent symptoms. Stereotaxic biopsy was performed in 17 pts (71%); 9 (53%) had grade II diffuse astrocytoma, and 3 (18%) pilocytic astrocytoma; glioblastoma (GBM) was found in 1 patient at diagnosis and in another at a late recurrence of a glial proliferation. Pons and bulb were the main sites of the tumor (N=10/10). Among the 21 treated pts, all underwent radiotherapy (RT); 7 received sequential radiotherapy and chemotherapy (RT+CT). Median OS was 45.2 months and 5-y OS was 48.7% (95% CI 24.5-69.2%). No statistically significant association was found between OS and age, tmt modality, or MRI contrast enhancement. ECOG-PS 3-4 was identified as negative PF; although no statistically significant, there was a numerical difference of outcomes regarding histological grade (Table). Table: 381P

FACTOR HR P 95% CI
Age (≥ vs < 40 ys) 0.957 0.943 0.29-3.15
ECOG-PS (3-4 vs 0-2) 5.31 0.030 1.17-24.14
Initial treatment RT RT+CT BSC Reference 1.28 7.75 - 0.730 0.028 - 0.31-5.25 1.24-48.25
Histologic type* (HG vs LG) 2.39 0.258 0.52-10.92
MRI contrast enhancement (Y vs N) 1.60 0.496 0.41-6.25
MRI restricted diffusion (Y vs N) 1.54 0.461 0.48-4.89

*HG (high-grade): anaplastic, GBM; LG (low-grade): LG, pilocytic, diffuse.

Conclusions

Diagnosis of BG using stereotaxic biopsy may be more feasible than historically assumed and diverse histologies were identified. ECOG-PS 3-4 was a negative prognostic factor. Multicenter collaborative efforts are warranted for a better evaluation of PFs, including molecular profile.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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