Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Feb 13;2(4):e114.
doi: 10.1002/hsr2.114. eCollection 2019 Apr.

Single-institution retrospective review of patients with recurrent glioblastoma treated with bevacizumab in clinical practice

Affiliations

Single-institution retrospective review of patients with recurrent glioblastoma treated with bevacizumab in clinical practice

Annick Desjardins et al. Health Sci Rep. .

Abstract

Background and aims: This retrospective review of patients with recurrent glioblastoma treated at the Preston Robert Tisch Brain Tumor Center investigated treatment patterns, survival, and safety with bevacizumab in a real-world setting.

Methods: Adult patients with glioblastoma who initiated bevacizumab at disease progression between January 1, 2009, and May 14, 2012, were included. A Kaplan-Meier estimator was used to describe overall survival (OS), progression-free survival (PFS), and time to greater than or equal to 20% reduction in Karnofsky Performance Status (KPS). The effect of baseline demographic and clinical factors on survival was examined using a Cox proportional hazards model. Adverse event (AE) data were collected.

Results: Seventy-four patients, with a median age of 59 years, were included in this cohort. Between bevacizumab initiation and first failure, defined as the first disease progression after bevacizumab initiation, biweekly bevacizumab and bevacizumab/irinotecan were the most frequently prescribed regimens. Median duration of bevacizumab treatment until failure was 6.4 months (range, 0.5-58.7). Median OS and PFS from bevacizumab initiation were 11.1 months (95% confidence interval [CI], 7.3-13.4) and 6.4 months (95% CI, 3.9-8.5), respectively. Median time to greater than or equal to 20% reduction in KPS was 29.3 months (95% CI, 13.8-∞). Lack of corticosteroid usage at the start of bevacizumab therapy was associated with both longer OS and PFS, with a median OS of 13.2 months (95% CI, 8.6-16.6) in patients who did not initially require corticosteroids versus 7.2 months (95% CI, 4.8-12.5) in those who did (P = 0.0382, log-rank), while median PFS values were 8.6 months (95% CI, 4.6-9.7) and 3.7 months (95% CI, 2.7-6.6), respectively (P = 0.0243, log-rank). Treatment failure occurred in 70 patients; 47 of whom received salvage therapy, and most frequently bevacizumab/carboplatin (7/47; 14.9%). Thirteen patients (18%) experienced a grade 3 AE of special interest for bevacizumab.

Conclusions: Treatment patterns and outcomes for patients with recurrent glioblastoma receiving bevacizumab in a real-world setting were comparable with those reported in prospective clinical trials.

Keywords: bevacizumab; real‐world setting; recurrent glioblastoma; survival; treatment patterns.

PubMed Disclaimer

Conflict of interest statement

Annick Desjardins has received grants or research support from Genentech, PTC Therapeutics, Celldex, Triphase Research and Development Corp, Eli Lilly and Co, Eisai, Symphogen A/S, Pfizer, and Orbus Therapeutic and is an advisory board member for Genentech; Arliene Ravelo is an employee of Genentech and owns stock options in Roche; Nicolas Sommer is an employee of Genentech and owns stock options in Roche; and the remaining authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Kaplan‐Meier curves of: A, overall survival from initiation of bevacizumab; B, overall survival from glioblastoma diagnosis; and C, progression‐free survival from initiation of bevacizumab. CI indicates confidence interval; OS, overall survival; PFS, progression‐free survival
Figure 2
Figure 2
Time to a greater than or equal to 20% reduction in KPS from initiation of bevacizumab‐based treatment. *Thirteen patients were missing their baseline and/or their post‐baseline KPS. CI indicates confidence interval; KPS, Karnofsky performance status
Figure 3
Figure 3
Patterns of treatment until bevacizumab failure

References

    1. Ohgaki H, Dessen P, Jourde B, et al. Genetic pathways to glioblastoma: a population‐based study. Cancer Res. 2004;64(19):6892‐6899. - PubMed
    1. Roy S, Lahiri D, Maji T, Biswas J. Recurrent glioblastoma: where we stand. South Asian J Cancer. 2015;4(4):163‐173. - PMC - PubMed
    1. Yung WK, Albright RE, Olson J, et al. A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse. Br J Cancer. 2000;83(5):588‐593. - PMC - PubMed
    1. Wong ET, Hess KR, Gleason MJ, et al. Outcomes and prognostic factors in recurrent glioma patients enrolled onto phase II clinical trials. J Clin Oncol. 1999;17(8):2572‐2578. - PubMed
    1. Lamszus K, Ulbricht U, Matschke J, Brockmann MA, Fillbrandt R, Westphal M. Levels of soluble vascular endothelial growth factor (VEGF) receptor 1 in astrocytic tumors and its relation to malignancy, vascularity, and VEGF‐A. Clin Cancer Res. 2003;9(4):1399‐1405. - PubMed

LinkOut - more resources