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Pseudoprogression in patients with glioblastoma: clinical relevance despite low incidence

机译:胶质母细胞瘤患者的假进展:尽管发生率低,但仍具有临床意义

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摘要

Background. According to the Response Assessment in Neuro-Oncology criteria, new enhancement within the radiation field on contrast enhanced T1-weighted images within 12 weeks after completion of radiotherapy should not qualify for progressive disease, since up to 50% of these cases may be pseudoprogression (PsP). To validate this concept, we assessed incidence and overall survival (OS) of patients with suspected and confirmed PsP dependent on different time intervals and definitions of PsP. Methods. Patients with newly diagnosed glioblastoma and an enhancement increase of at least 25% after completion of standard radiochemotherapy at month 1, 4, 7, or 10 were eligible. Based on the development of the enhancement in follow-up examinations, patients were categorized as either PsP (subgrouped as complete resolution/decrease >50% and decrease <50%/stable) or true progression. Results. Out of 548 patients, 79 fulfilled the inclusion criteria. Of these 79 patients, 9 (11.4%) showed PsP (6/45 patients at 1 month, 2/17 at 4 months, 1/9 at 7 months, and 0/8 at 10 months). Complete resolution of the enhancement was found in 1, decrease >50% in 3, decrease <50% in 2, and stable enhancement in 3 patients with PsP. Patients with PsP showed a significantly longer OS (P< .012). No difference in OS was found among PsP subgroups. Conclusions. This series challenges the current concept of PsP. Even though we could confirm a prolonged OS of patients with PsP, the incidence of PsP was lower than reported previously and extended beyond 12 weeks.
机译:背景。根据神经肿瘤学反应评估标准,在放疗完成后12周内,对比增强的T1加权图像在放射野内的新增强不符合进行性疾病的标准,因为这些病例中多达50%可能是假进展( PsP)。为了验证这一概念,我们根据不同的时间间隔和PsP的定义评估了疑似和确诊的PsP患者的发生率和总生存期(OS)。方法。新诊断为胶质母细胞瘤且在第1、4、7或10个月完成标准放射化学治疗后增强至少增加25%的患者符合条件。根据随访检查增强的进展,将患者分为PsP(分组为完全缓解/降低> 50%,降低为<50%/稳定)或真实进展。结果。在548例患者中,有79例符合纳入标准。在这79位患者中,有9位(11.4%)显示PsP(1个月时为6 / 45,4个月时为2 / 17,7个月时为1 / 9,10个月时为0/8)。 PsP患者中有1例完全增强,而3例中> 50%下降,2例中<50%下降,3例PsP患者稳定增强。 PsP患者的OS明显更长(P <.012)。在PsP子组之间未发现OS差异。结论。本系列挑战了PsP的当前概念。即使我们可以确定PsP患者的OS延长,但PsP的发生率却比以前报道的要低,并且延长了12周以上。

著录项

  • 来源
    《Neuro-Oncology》 |2015年第1期|151-159|共9页
  • 作者单位

    Department of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany, University of Heidelberg, Department of Neuroradiology, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany;

    Department of Neuroradiology, University of Heidelberg, Heidelberg, Germany;

    Department of Neuroradiology, University of Heidelberg, Heidelberg, Germany;

    Department of Neurooncology, Neurology Clinic and National Center for Tumor Diseases, University of Heidelberg, Heidelberg, Germany ,German Cancer Consortium (DKTK) Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany;

    Department of Neurology, Innsbruck Medical University, Innsbruck, Austria;

    Department of Neuroradiology, University of Heidelberg, Heidelberg, Germany;

    Department of Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany;

    Department of Neurooncology, Neurology Clinic and National Center for Tumor Diseases, University of Heidelberg, Heidelberg, Germany ,German Cancer Consortium (DKTK) Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany;

    Department of Neuroradiology, University of Heidelberg, Heidelberg, Germany;

    Department of Neurooncology, Neurology Clinic and National Center for Tumor Diseases, University of Heidelberg, Heidelberg, Germany ,German Cancer Consortium (DKTK) Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany;

    Department of Neuroradiology, University of Heidelberg, Heidelberg, Germany;

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  • 正文语种 eng
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  • 关键词

    glioblastoma; pseudoprogression;

    机译:胶质母细胞瘤伪进展;

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