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A multicenter phase II study of temozolomide plus disulfiram and copper for recurrent temozolomide-resistant glioblastoma.
Huang, Jiayi; Chaudhary, Rekha; Cohen, Adam L; Fink, Karen; Goldlust, Samuel; Boockvar, John; Chinnaiyan, Prakash; Wan, Leping; Marcus, Stephen; Campian, Jian L.
Afiliação
  • Huang J; Washington University School of Medicine, St. Louis, MO, USA. jiayi.huang@wustl.edu.
  • Chaudhary R; Department of Radiation Oncology, Center for Advanced Medicine, Washington University School of Medicine, 4921 Parkview Place, Campus Box #8224, St. Louis, MO, 63110, USA. jiayi.huang@wustl.edu.
  • Cohen AL; University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Fink K; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Goldlust S; Baylor University Medical Center, Dallas, TX, USA.
  • Boockvar J; Hackensack University Medical Center, Hackensack, NJ, USA.
  • Chinnaiyan P; Lenox Hill Hospital, New York, NY, USA.
  • Wan L; Beaumont Health, Royal Oak, MI, USA.
  • Marcus S; Washington University School of Medicine, St. Louis, MO, USA.
  • Campian JL; Cantex Pharmaceuticals, Weston, FL, USA.
J Neurooncol ; 142(3): 537-544, 2019 May.
Article em En | MEDLINE | ID: mdl-30771200
ABSTRACT

PURPOSE:

Preclinical studies have suggested promising activity for the combination of disulfiram and copper (DSF/Cu) against glioblastoma (GBM) including re-sensitization to temozolomide (TMZ). A previous phase I study demonstrated the safety of combining DSF/Cu with adjuvant TMZ for newly diagnosed GBM. This phase II study aimed to estimate the potential effectiveness of DSF/Cu to re-sensitize recurrent GBM to TMZ.

METHODS:

This open-label, single-arm phase II study treated recurrent TMZ-resistant GBM patients with standard monthly TMZ plus concurrent daily DSF 80 mg PO TID and Cu 1.5 mg PO TID. Eligible patients must have progressed after standard chemoradiotherapy and within 3 months of the last dose of TMZ. Known isocitrate dehydrogenase (IDH) mutant or secondary GBMs were excluded. The primary endpoint was objective response rate (ORR), and the secondary endpoints included progression-free survival (PFS), overall survival (OS), clinical benefit (response or stable disease for at least 6 months), and safety.

RESULTS:

From March 2017 to January 2018, 23 recurrent TMZ-resistant GBM patients were enrolled across seven centers, and 21 patients were evaluable for response. The median duration of DSF/Cu was 1.6 cycles (range 0.1-12.0). The ORR was 0%, but 14% had clinical benefit. Median PFS was 1.7 months, and median OS was 7.1 months. Only one patient (4%) had dose-limiting toxicity (grade three elevated alanine transaminase).

CONCLUSIONS:

Addition of DSF/Cu to TMZ for TMZ-resistant IDH-wild type GBM appears well tolerated but has limited activity for unselected population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Protocolos de Quimioterapia Combinada Antineoplásica / Glioblastoma / Resistencia a Medicamentos Antineoplásicos / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Protocolos de Quimioterapia Combinada Antineoplásica / Glioblastoma / Resistencia a Medicamentos Antineoplásicos / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article