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Evaluation of potential circulating biomarkers for prediction of response to chemoradiation in patients with glioblastoma.
van Linde, Myra E; van der Mijn, Johannes C; Pham, Thang V; Knol, Jaco C; Wedekind, Laurine E; Hovinga, Koos E; Aliaga, Esther Sanchez; Buter, Jan; Jimenez, Connie R; Reijneveld, Jaap C; Verheul, Henk M W.
Afiliación
  • van Linde ME; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • van der Mijn JC; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Pham TV; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Knol JC; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Wedekind LE; Department of Neurosurgery, Neuro-oncology Research Group, VU University Medical Center, Amsterdam, The Netherlands.
  • Hovinga KE; Department of Neurosurgery, VU University Medical Center, Amsterdam, The Netherlands.
  • Aliaga ES; Department of Radiology, VU University Medical Center, Amsterdam, The Netherlands.
  • Buter J; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Jimenez CR; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Reijneveld JC; Department of Neurology, VU University Medical Center, Amsterdam, The Netherlands.
  • Verheul HM; Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands. h.verheul@vumc.nl.
J Neurooncol ; 129(2): 221-30, 2016 09.
Article en En | MEDLINE | ID: mdl-27444431
Surgery followed by chemoradiation and adjuvant chemotherapy is standard of care for patients with a glioblastoma (GBM). Due to its limited benefit, an upfront method to predict dismal outcome would prevent unnecessary toxic treatment. We searched for a predictive blood derived biomarker in a cohort of 55 patients with GBM. Increasing age (HR 1.03, 95 % CI 1.01-1.06), and postoperative tumor residue (HR 1.07, 95 % CI 1.02-1.15) were independently associated with unfavourable progression free survival (PFS) in these patients. Corticosteroid use before start of chemoradiaton was strongly predictive for outcome (HR 3.26, 95 % CI 1.67-6.39) with a mean PFS and OS in patients using corticosteroids of 7.3 and 14.6 months, versus 16.1 and 21.6 months in patients not using corticosteroids (p = 0.0005, p < 0.0067 respectively). Despite earlier reports, blood concentrations of YKL-40, Fetuin-a and haptoglobin were not predictive for response. In addition, serum peptide profiles, determined by MALDI-TOF mass spectroscopy, were not predictive as well. In conclusion, further biomarker discovery studies are needed to predict treatment outcome for patients with GBM in the near future.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Alfa-2-Glicoproteína-HS / Quimioradioterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Alfa-2-Glicoproteína-HS / Quimioradioterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos