Literature DB >> 31386050

Bevacizumab at first recurrence after standard radio-chemotherapy is associated with improved overall survival in glioblastoma patients with large tumor burden.

Huy Tram Nguyen1, Nhung Nguyen1, Liang Yen Liu1, Laura Dovek1, Daniel Lenchner1, Robert Harris2, Byram Ozer1, Arliene Ravelo3, Nicolas Sommer3, Myung Shin Sim4, Robert Elashoff4, Richard Green5, Phioanh Leia Nghiemphu1, Timothy Francis Cloughesy1, Benjamin Ellingson2, Albert Lai1.   

Abstract

BACKGROUND: Since its approval for use in recurrent glioblastoma (GBM), the survival benefit of bevacizumab (Bev) remains to be demonstrated. To address this issue, we retrospectively examined survival from first recurrence in patients treated with Bev, lomustine (CCNU), or Bev/CCNU.
METHODS: We identified 168 primary GBM patients diagnosed at UCLA and Kaiser Permanente LA who received upfront radio-chemotherapy, followed by Bev and/or CCNU at first recurrence. Three patient groups, contemporaneously diagnosed from 2009 through 2015, were identified: (1) patients treated with Bev alone (n = 49), (2) CCNU alone (CCNU 09-15) (n = 36), and (3) Bev/CCNU (n = 53). Another CCNU control group (n = 30) diagnosed from 2001 through 2004 (CCNU 01-04) was also derived. We measured tumor size at first recurrence treatment initiation, using bidimensional (2D) and volumetric (3D) techniques, and analyzed overall survival (OS) from first recurrence.
RESULTS: Among the entire cohort, larger tumor size at first recurrence was associated with poorer survival. The CCNU 01-04 group had similar tumor size as the Bev arms and low Bev crossover (7%). Treatment with Bev was associated with improved survival in patients with large tumor 2D measurements: Median OS for Bev and Bev/CCNU groups were 6.71 mo (n = 27) and 6.97 mo (n = 36) vs 4.03 mo (n = 10) in CCNU 01-04. Analysis by 3D measurement yielded similar results. Interestingly, the CCNU 09-15 group showed the highest survival, likely due to smaller tumor size and crossover to Bev (69%).
CONCLUSION: Survival advantage from Bev treatment was observed only among patients with large tumor burden as determined by either 2D or 3D measurement.

Entities:  

Keywords:  bevacizumab; first recurrence; glioblastoma; overall survival; tumor size

Year:  2018        PMID: 31386050      PMCID: PMC6656330          DOI: 10.1093/nop/npy021

Source DB:  PubMed          Journal:  Neurooncol Pract        ISSN: 2054-2577


  10 in total

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3.  Measurement of tumor "size" in recurrent malignant glioma: 1D, 2D, or 3D?

Authors:  Mary F Dempsey; Barrie R Condon; Donald M Hadley
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4.  Criteria for evaluating patients undergoing chemotherapy for malignant brain tumors.

Authors:  V A Levin; D C Crafts; D M Norman; P B Hoffer; J P Spire; C B Wilson
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5.  Single-agent bevacizumab or lomustine versus a combination of bevacizumab plus lomustine in patients with recurrent glioblastoma (BELOB trial): a randomised controlled phase 2 trial.

Authors:  Walter Taal; Hendrika M Oosterkamp; Annemiek M E Walenkamp; Hendrikus J Dubbink; Laurens V Beerepoot; Monique C J Hanse; Jan Buter; Aafke H Honkoop; Dolf Boerman; Filip Y F de Vos; Winand N M Dinjens; Roelien H Enting; Martin J B Taphoorn; Franchette W P J van den Berkmortel; Rob L H Jansen; Dieta Brandsma; Jacoline E C Bromberg; Irene van Heuvel; René M Vernhout; Bronno van der Holt; Martin J van den Bent
Journal:  Lancet Oncol       Date:  2014-07-15       Impact factor: 41.316

6.  Lomustine and Bevacizumab in Progressive Glioblastoma.

Authors:  Wolfgang Wick; Thierry Gorlia; Martin Bendszus; Martin Taphoorn; Felix Sahm; Inga Harting; Alba A Brandes; Walter Taal; Julien Domont; Ahmed Idbaih; Mario Campone; Paul M Clement; Roger Stupp; Michel Fabbro; Emilie Le Rhun; Francois Dubois; Michael Weller; Andreas von Deimling; Vassilis Golfinopoulos; Jacoline C Bromberg; Michael Platten; Martin Klein; Martin J van den Bent
Journal:  N Engl J Med       Date:  2017-11-16       Impact factor: 91.245

7.  Prognostic factors in recurrent glioblastoma multiforme and anaplastic astrocytoma treated with selective intra-arterial chemotherapy.

Authors:  K L Chow; Y P Gobin; T Cloughesy; J W Sayre; J P Villablanca; F Viñuela
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8.  Phase II study of bevacizumab plus temozolomide during and after radiation therapy for patients with newly diagnosed glioblastoma multiforme.

Authors:  Albert Lai; Anh Tran; Phioanh L Nghiemphu; Whitney B Pope; Orestes E Solis; Michael Selch; Emese Filka; William H Yong; Paul S Mischel; Linda M Liau; Surasak Phuphanich; Keith Black; Scott Peak; Richard M Green; Cynthia E Spier; Tatjana Kolevska; Jonathan Polikoff; Louis Fehrenbacher; Robert Elashoff; Timothy Cloughesy
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9.  Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma.

Authors:  Roger Stupp; Warren P Mason; Martin J van den Bent; Michael Weller; Barbara Fisher; Martin J B Taphoorn; Karl Belanger; Alba A Brandes; Christine Marosi; Ulrich Bogdahn; Jürgen Curschmann; Robert C Janzer; Samuel K Ludwin; Thierry Gorlia; Anouk Allgeier; Denis Lacombe; J Gregory Cairncross; Elizabeth Eisenhauer; René O Mirimanoff
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10.  Maintenance Therapy With Tumor-Treating Fields Plus Temozolomide vs Temozolomide Alone for Glioblastoma: A Randomized Clinical Trial.

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  10 in total
  1 in total

1.  Patterns of long-term survivorship following bevacizumab treatment for recurrent glioma: a case series.

Authors:  Liang Yen Liu; Matthew S Ji; Nhung T Nguyen; Frances E Chow; Donna M Molaie; Sean T Pianka; Richard M Green; Linda M Liau; Benjamin M Ellingson; Phioanh L Nghiemphu; Timothy F Cloughesy; Albert Lai
Journal:  CNS Oncol       Date:  2019-07-11
  1 in total

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