Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

ePoster Display

360P - Metronomic temozolomide therapy in heavily pretreated patients with recurrent glioblastoma: A large mono-institutional retrospective study

Date

16 Sep 2021

Session

ePoster Display

Topics

Clinical Research;  Rare Cancers

Tumour Site

Central Nervous System Malignancies

Presenters

Vittorina Zagonel

Citation

Annals of Oncology (2021) 32 (suppl_5): S516-S529. 10.1016/annonc/annonc674

Authors

A. Bosio1, G. Cerretti2, M. Padovan2, M. Caccese2, V. Guarneri3, V. Zagonel4, G. Lombardi2

Author affiliations

  • 1 Oncology, University of Padua - School of Medicine, 35128 - Padova/IT
  • 2 Department Of Oncology, Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padua/IT
  • 3 Department Of Surgery, Oncology And Gastroenterology, University Of Padova, Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova/IT
  • 4 Department Of Oncology, Oncology 1, Veneto Institute of Oncology IOV-IRCCS, 000 - Padua/IT

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 360P

Background

Glioblastoma (GBM) is the most common and aggressive primary brain cancer. Despite advances in surgical and first-line treatment, all pts relapse. The aim of this study is to evaluate the benefit of metronomic Temozolomide (mTMZ) for recurrent GBM.

Methods

All pts treated at Veneto Institute of Oncology from September 2013 to March 2021 were retrospectively reviewed. Major inclusion criteria were: first-line therapy with Stupp protocol, relapse after first or subsequent line of therapy, treatment with mTMZ schedule (50mg/m2 continuously), hystologically confirmed diagnosis of GBM. RANO criteria and CTCAE v 5.0 were used for response and toxicity assessment.

Results

120 pts were enrolled. Median follow-up was 15.6ms. Median age was 59ys (range 18-81), ECOG PS was 0-2 in 107 patients (89%) and 3 in 11 (9%). MGMT was methylated and IDH mutated in 66 of 105 (62%) and in 9 of 106 (8%) evaluable pts, respectively. Median number of prior lines of treatment was 2 (range 1-7) and 41% of pts received the therapy beyond the third line. Median time between the last standard maintenance TMZ (sTMZ) cycle and the mTMZ administration was 6ms (range 1-50) and 40% of pts started mTMZ after 3ms from sTMZ. All pts were evaluable for response: 3 (2%) and 48 (40%) showed PR and SD. mOS from the start of mTMZ was 5.4ms (95% CI 4.3-6.4), mPFS was 2.6ms (95% CI 2.3-2.8). On univariate analysis, MGMTmet and MGMTunmet pts had a mOS of 5.6 and 4.4ms (p=0.03); mOS for patients with ECOG PS > or ≤2 was 2.3 and 6.0 ms (p<0.001); number of prior lines of therapies, time between sTMZ and mTMZ and age were not significant. On multivariate analysis, MGMT methylated status (HR=2.3, 95% CI, p=0.004) and ECOG PS (HR=0.5, 95% CI, p=0.017) remained statistically significant for PFS, while ECOG PS (HR=0.4, 95% CI, p=0.001) was the only factor significantly associated with OS. The most common grade 3 and 4 hematologic toxicities were lymphopenia (10%) and thrombocytopenia (3%). Grade 3 and 4 nonhematologic toxicities were uncommon.

Conclusions

Rechallenge with mTMZ can be a well tolerated treatment option for recurrent GBM, even in heavily pretreated pts. Pts with MGMTmet and good ECOG PS might report the major benefit.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.