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Cell-free DNA in newly diagnosed patients with glioblastoma - a clinical prospective feasibility study.
Nørøxe, Dorte Schou; Østrup, Olga; Yde, Christina Westmose; Ahlborn, Lise Barlebo; Nielsen, Finn Cilius; Michaelsen, Signe Regner; Larsen, Vibeke Andrée; Skjøth-Rasmussen, Jane; Brennum, Jannick; Hamerlik, Petra; Poulsen, Hans Skovgaard; Lassen, Ulrik.
Afiliação
  • Nørøxe DS; Department of Radiation Biology, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Østrup O; Department of Oncology, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Yde CW; Center for Genomic Medicine, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Ahlborn LB; Center for Genomic Medicine, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Nielsen FC; Center for Genomic Medicine, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Michaelsen SR; Center for Genomic Medicine, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Larsen VA; Department of Radiation Biology, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Skjøth-Rasmussen J; Department of Neuroradiology, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Brennum J; Department of Neurosurgery, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Hamerlik P; Department of Neurosurgery, Rigshospitalet, 2100 Copenhagen, Denmark.
  • Poulsen HS; Danish Cancer Society, 2100 Copenhagen, Denmark.
  • Lassen U; Department of Radiation Biology, Rigshospitalet, 2100 Copenhagen, Denmark.
Oncotarget ; 10(43): 4397-4406, 2019 07 09.
Article em En | MEDLINE | ID: mdl-31320993
Background: Glioblastoma (GB) is an incurable brain cancer with limited treatment options. The aim was to test the feasibility of using cell-free DNA (cfDNA) to support evaluation of treatment response, pseudo-progression and whether progression could be found before clinical and/or radiologic progression. Results: CfDNA fluctuated during treatment with the highest levels before diagnostic surgery and at progression. An increase was seen in 3 out of 4 patients at the time of progression while no increase was seen in 3 out of 4 patients without progression. CfDNA levels could aid in 3 out of 3 questionable cases of pseudo-progression. Methods: Eight newly diagnosed GB patients were included. Blood samples were collected prior to diagnosis, before start and during oncologic treatment until progression. Seven patients received concurrent radiotherapy/Temozolomide with adjuvant Temozolomide with one of the patients included in a clinical trial with either immunotherapy or placebo as add-on. One patient received radiation alone. CfDNA concentration was determined for each blood sample. Conclusions: It was feasible to measure cfDNA concentration. Despite the limited cohort size, there was a good tendency between cfDNA and treatment course and -response, respectively with the highest levels at progression.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article