Literature DB >> 26721240

Adverse event grading following CTCAE v3.0 underestimates hypertensive side effects in patients with glioma treated with Bevacizumab.

Elisabeth Bumes1, Sarah Rzonsa1, Markus Hutterer1, Martin Proescholdt2, Ulrich Bogdahn1, Markus J Riemenschneider3, Martin Uhl4, Christina Wendl5, Peter Hau6.   

Abstract

Anti-VEGF therapy with Bevacizumab (BEV) is widely used in cases of relapsed high-grade glioma (HGG). Arterial hypertension is a known side effect of anti-VEGF therapy. 42 Patients with relapsed HGG were treated with BEV 10 mg/kg on days 1 and 15 of 28-day cycles in addition to treatment with 40 mg TMZ daily until disease progression, based on magnetic resonance imaging and/or worsening of clinical status. In a retrospective analysis, hypertensive side effects were evaluated as the primary endpoint, while survival information in addition to toxicity was analyzed as secondary endpoint. Grading which employs the Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 detected hypertensive events with a significantly higher sensitivity than CTCAE version 3.0. The rate of severe hypertensive events observed as CTCAE ≥ °3 were 9.5 % in version 3.0 and 45.2 % in version 4.0. The results presented here indicate that CTCAE version 3.0 may underreport the incidence and grade of BEV-induced hypertension within clinical trials. As hypertension has not only long-term, but also severe short-term side effects, we suggest that arterial hypertension under BEV should be scored according to CTCAE version 4.0 to avoid clinically relevant hypertension-related adverse events in these patients.

Entities:  

Keywords:  Bevacizumab; CTCAE; Glioblastoma; High-grade glioma; Hypertension; Temozolomide

Mesh:

Substances:

Year:  2015        PMID: 26721240     DOI: 10.1007/s11060-015-2031-7

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  38 in total

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Authors:  Babak Nazer; Benjamin D Humphreys; Javid Moslehi
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Review 2.  Hypertension as a biomarker in patients with recurrent glioblastoma treated with antiangiogenic drugs: a single-center experience and a critical review of the literature.

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Journal:  Anticancer Drugs       Date:  2013-01       Impact factor: 2.248

Review 3.  Cardiovascular safety of VEGF-targeting therapies: current evidence and handling strategies.

Authors:  Fabio Girardi; Enrico Franceschi; Alba A Brandes
Journal:  Oncologist       Date:  2010-06-14

4.  Phase II study of bevacizumab in combination with sorafenib in recurrent glioblastoma (N0776): a north central cancer treatment group trial.

Authors:  Evanthia Galanis; S Keith Anderson; Jackie M Lafky; Joon H Uhm; Caterina Giannini; Shaji K Kumar; Teresa K Kimlinger; Donald W Northfelt; Patrick J Flynn; Kurt A Jaeckle; Timothy J Kaufmann; Jan C Buckner
Journal:  Clin Cancer Res       Date:  2013-07-05       Impact factor: 12.531

5.  Phase II trial of continuous dose-intense temozolomide in recurrent malignant glioma: RESCUE study.

Authors:  James R Perry; Karl Bélanger; Warren P Mason; Dorcas Fulton; Petr Kavan; Jacob Easaw; Claude Shields; Sarah Kirby; David R Macdonald; David D Eisenstat; Brian Thiessen; Peter Forsyth; Jean-François Pouliot
Journal:  J Clin Oncol       Date:  2010-03-22       Impact factor: 44.544

6.  Phase 2 study of carboplatin, irinotecan, and bevacizumab for recurrent glioblastoma after progression on bevacizumab therapy.

Authors:  David A Reardon; Annick Desjardins; Katherine B Peters; James J Vredenburgh; Sridharan Gururangan; John H Sampson; Roger E McLendon; James E Herndon; April Coan; Stevie Threatt; Allan H Friedman; Henry S Friedman
Journal:  Cancer       Date:  2011-05-16       Impact factor: 6.860

7.  Bevacizumab plus irinotecan in recurrent or progressive malign glioma: a multicenter study of the Anatolian Society of Medical Oncology (ASMO).

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Journal:  J Cancer Res Clin Oncol       Date:  2013-02-12       Impact factor: 4.553

8.  Phase II trial of single-agent bevacizumab followed by bevacizumab plus irinotecan at tumor progression in recurrent glioblastoma.

Authors:  Teri N Kreisl; Lyndon Kim; Kraig Moore; Paul Duic; Cheryl Royce; Irene Stroud; Nancy Garren; Megan Mackey; John A Butman; Kevin Camphausen; John Park; Paul S Albert; Howard A Fine
Journal:  J Clin Oncol       Date:  2008-12-29       Impact factor: 44.544

9.  Phase II study of single-agent bevacizumab in Japanese patients with recurrent malignant glioma.

Authors:  Motoo Nagane; Ryo Nishikawa; Yoshitaka Narita; Hiroyuki Kobayashi; Shingo Takano; Nobusada Shinoura; Tomokazu Aoki; Kazuhiko Sugiyama; Junichi Kuratsu; Yoshihiro Muragaki; Yutaka Sawamura; Masao Matsutani
Journal:  Jpn J Clin Oncol       Date:  2012-07-27       Impact factor: 3.019

10.  Activity and safety of bevacizumab plus fotemustine for recurrent malignant gliomas.

Authors:  V Vaccaro; A Fabi; A Vidiri; D Giannarelli; G Metro; S Telera; S Vari; F Piludu; M A Carosi; V Villani; F Cognetti; A Pompili; L Marucci; C M Carapella; A Pace
Journal:  Biomed Res Int       Date:  2014-05-04       Impact factor: 3.411

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