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Acetazolamide versus placebo for cerebral oedema requiring dexamethasone in recurrent and/or progressive high-grade glioma: phase II randomised placebo-controlled double-blind study.
Agar, Meera R; Nowak, Anna K; Hovey, Elizabeth J; Barnes, Elizabeth H; Simes, John; Vardy, Janette L; Wheeler, Helen R; Kong, Benjamin Y; Leonard, Robyn; Hall, Merryn; Tim, Evonne; Spyridopoulos, Desma; Sim, Hao-Wen; Lwin, Zarnie; Dowling, Anthony; Harrup, Rosemary; Jennens, Ross; Kichenadasse, Ganessan; Dunlop, Tracey; Gzell, Cecelia; Koh, Eng-Siew.
Afiliação
  • Agar MR; Palliative Care, Liverpool Hospital, Liverpool, New South Wales, Australia meera.agar@uts.edu.au.
  • Nowak AK; Health, University of Technology Sydney, Sydney, New South Wales, Australia.
  • Hovey EJ; Medical Oncology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Barnes EH; Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
  • Simes J; Nelune Comprehensive Cancer Centre, Prince of Wales Hospital, Randwick, New South Wales, Australia.
  • Vardy JL; Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.
  • Wheeler HR; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Kong BY; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Leonard R; Medical Oncology, Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia.
  • Hall M; Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
  • Tim E; Medical Oncology, Concord Repatriation General Hospital, Concord, New South Wales, Australia.
  • Spyridopoulos D; Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
  • Sim HW; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Lwin Z; Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
  • Dowling A; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Harrup R; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Jennens R; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Kichenadasse G; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Dunlop T; NHMRC Clinical Trials Centre, Camperdown, New South Wales, Australia.
  • Gzell C; Medical Oncology, Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia.
  • Koh ES; Medical Oncology, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.
BMJ Support Palliat Care ; 13(3): 354-362, 2023 Sep.
Article em En | MEDLINE | ID: mdl-36807048
ABSTRACT

OBJECTIVES:

Symptoms of raised intracranial pressure (ICP) in recurrent high-grade glioma (HGG) generally require corticosteroid treatment, often causing toxicity with variable effects on ICP symptoms. Acetazolamide reduces ICP when used in other clinical non-cancer settings. The aim of the study was to explore whether the addition of oral acetazolamide enables safe dexamethasone dose reduction in management of raised ICP in recurrent HGG.

METHODS:

Participants had recurrent HGG with any of dexamethasone recommencement, dose increase or dependency; prior/current bevacizumab was an exclusion. Eligible participants were randomised 11 to acetazolamide or placebo for 8 weeks. Standardised protocols were used for dexamethasone dosing, with planned dose decrease from day 5 once ICP symptoms were stable. The primary endpoint was a composite of dexamethasone dose reduction and stable Karnofsky Performance Status Secondary endpoints included toxicity and feasibility.

RESULTS:

Thirty participants (15 per group) were enrolled (mean age 58 years) from seven Australian sites. The mean baseline dexamethasone dose was 6.2 mg. Mean duration on study treatment was 38 days (placebo group) and 31 days (acetazolamide group) with nine participants (30%) completing all study treatments (six placebo, three acetazolamide). Study withdrawal was due to adverse events (n=6; one placebo, five acetazolamide) and disease progression (n=6 (three per arm)). Four participants (13%) (two per arm) were stable responders. Ten participants experienced a total of 13 serious adverse events (acetazolamide arm five participants (33%), six events, two related).

CONCLUSIONS:

The study closed early due to poor accrual and increasing availability of bevacizumab. The addition of acetazolamide did not facilitate dexamethasone reduction. TRIAL REGISTRATION NUMBER ACTRN12615001072505.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Problema de saúde: 1_doencas_nao_transmissiveis / 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: Edema Encefálico / Glioma Tipo de estudo: Clinical_trials / Etiology_studies / Guideline Aspecto: Patient_preference Limite: Humans / Middle aged País/Região como assunto: Oceania Idioma: En Revista: BMJ Support Palliat Care Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Problema de saúde: 1_doencas_nao_transmissiveis / 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: Edema Encefálico / Glioma Tipo de estudo: Clinical_trials / Etiology_studies / Guideline Aspecto: Patient_preference Limite: Humans / Middle aged País/Região como assunto: Oceania Idioma: En Revista: BMJ Support Palliat Care Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália
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