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      Incidence of pseudoprogression in low-grade gliomas treated with radiotherapy

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          Abstract

          Background.

          As the incidence of pseudo-progressive disease (psPD), or pseudoprogression, in low-grade glioma (LGG) is unknown, we retrospectively investigated this phenomenon in a cohort of LGG patients given radiotherapy (RT).

          Methods.

          All MRI scans and clinical data from patients with histologically proven LGG treated with radiation between 2000 and 2011 were reviewed. PsPD was scored when a new enhancing lesion occurred after RT and subsequently disappeared or remained stable for at least a year without therapy, including dexamethasone.

          Results.

          Sixty-three out of 71 patients who received RT for LGG were deemed eligible for evaluation of psPD. The median follow-up was 5 years (range 1‒10 y). PsPD was seen in 13 patients (20.6%). PsPD occurred after a median of 12 months with a range of 3–78 months. The median duration of psPD was 6 months, with a range of 2–26 months and always occurred within the RT high dose fields of at least 45 Gy. The area of the enhancement at the time of psPD was significantly smaller compared with the area of enhancement during “true” progression (median size 54mm 2 [range 12–340mm 2] vs 270mm 2 [range 30–3420mm 2], respectively; P = .009).

          Conclusions.

          PsPD occurs frequently in LGG patients receiving RT. This supports the policy to postpone a new line of treatment until progression is evident, especially when patients have small contrast enhancing lesions within the RT field.

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          Author and article information

          Journal
          Neuro Oncol
          Neuro-oncology
          neuonc
          Neuro-Oncology
          Oxford University Press (US )
          1522-8517
          1523-5866
          May 2017
          21 September 2016
          : 19
          : 5
          : 719-725
          Affiliations
          [1 ] Department of Neuro-oncology/Neurology, Erasmus MC Cancer Institute , Rotterdam, Netherlands (S.E.v.W., B.v.d.L., M.J.v.d.B., W.T.); Department of Radiology, Erasmus MC Cancer Institute , Rotterdam, Netherlands (H.G.d.B.; retired);
          Author notes

          Current affiliation: Department of Neurology, Bernhoven Hospital, Uden, Netherlands (B.v.d.L.); Department of Radiotherapy, Erasmus MC Cancer Institute, Rotterdam, Netherlands (A.T.S.-K.)

          Corresponding Author: Walter Taal, MD, Department of Neuro-oncology/Neurology, Erasmus MC Cancer Institute, Groene Hilledijk 301, 3075 EA Rotterdam, The Netherlands ( w.taal@ 123456erasmusmc.nl ).

          Article
          PMC5464441 PMC5464441 5464441 now194
          10.1093/neuonc/now194
          5464441
          28453748
          eb857ce4-1f32-4e5b-850c-df5498f8cc62
          © The Author(s) 2016. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
          History
          : 26 April 2016
          : 01 August 2016
          Page count
          Pages: 6
          Categories
          Neuroimaging

          glioma,LGG,low-grade glioma,pseudoprogression,radiotherapy.
          glioma, LGG, low-grade glioma, pseudoprogression, radiotherapy.

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