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本文引用的文献

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Magnetic Resonance Imaging of Glioma in the Era of Antiangiogenic Therapy.抗血管生成治疗时代的胶质瘤磁共振成像
PET Clin. 2013 Apr;8(2):163-82. doi: 10.1016/j.cpet.2012.09.004. Epub 2012 Dec 1.
2
Progression types after antiangiogenic therapy are related to outcome in recurrent glioblastoma.抗血管生成治疗后的进展类型与复发性胶质母细胞瘤的结局相关。
Neurology. 2014 May 13;82(19):1684-92. doi: 10.1212/WNL.0000000000000402. Epub 2014 Apr 11.
3
CBTRUS statistical report: Primary brain and central nervous system tumors diagnosed in the United States in 2006-2010.CBTRUS统计报告:2006 - 2010年在美国诊断出的原发性脑和中枢神经系统肿瘤
Neuro Oncol. 2013 Nov;15 Suppl 2(Suppl 2):ii1-56. doi: 10.1093/neuonc/not151.
4
FLAIR-only progression in bevacizumab-treated relapsing glioblastoma does not predict short survival.贝伐珠单抗治疗后复发性胶质母细胞瘤仅 FLAIR 进展并不预示着生存期短。
Oncology. 2013;85(3):191-5. doi: 10.1159/000354692. Epub 2013 Sep 5.
5
Early post-bevacizumab progression on contrast-enhanced MRI as a prognostic marker for overall survival in recurrent glioblastoma: results from the ACRIN 6677/RTOG 0625 Central Reader Study.贝伐珠单抗治疗后早期增强 MRI 进展作为复发性胶质母细胞瘤总生存期的预后标志物:来自 ACRIN 6677/RTOG 0625 中心读片研究的结果。
Neuro Oncol. 2013 Jul;15(7):945-54. doi: 10.1093/neuonc/not049. Epub 2013 Jun 19.
6
Differentiation of true progression from pseudoprogression in glioblastoma treated with radiation therapy and concomitant temozolomide: comparison study of standard and high-b-value diffusion-weighted imaging.在接受放疗和替莫唑胺联合治疗的胶质母细胞瘤中,从假性进展中区分真性进展:标准和高 b 值扩散加权成像的对比研究。
Radiology. 2013 Dec;269(3):831-40. doi: 10.1148/radiol.13122024. Epub 2013 Oct 28.
7
Response assessment criteria for glioblastoma: practical adaptation and implementation in clinical trials of antiangiogenic therapy.胶质母细胞瘤的反应评估标准:抗血管生成治疗临床试验中的实际调整和实施。
Curr Neurol Neurosci Rep. 2013 May;13(5):347. doi: 10.1007/s11910-013-0347-2.
8
Standards of care for treatment of recurrent glioblastoma--are we there yet?复发性胶质母细胞瘤治疗的护理标准——我们做到了吗?
Neuro Oncol. 2013 Jan;15(1):4-27. doi: 10.1093/neuonc/nos273. Epub 2012 Nov 7.
9
Phase III trial of chemoradiotherapy for anaplastic oligodendroglioma: long-term results of RTOG 9402.三期临床试验:放化疗治疗间变性少突胶质细胞瘤:RTOG9402 的长期结果。
J Clin Oncol. 2013 Jan 20;31(3):337-43. doi: 10.1200/JCO.2012.43.2674. Epub 2012 Oct 15.
10
Adjuvant procarbazine, lomustine, and vincristine chemotherapy in newly diagnosed anaplastic oligodendroglioma: long-term follow-up of EORTC brain tumor group study 26951.替莫唑胺辅助治疗新诊断的间变性少突胶质细胞瘤:欧洲癌症研究与治疗组织脑肿瘤研究组 26951 号研究的长期随访。
J Clin Oncol. 2013 Jan 20;31(3):344-50. doi: 10.1200/JCO.2012.43.2229. Epub 2012 Oct 15.

当前脑肿瘤成像的利弊

Pros and cons of current brain tumor imaging.

作者信息

Ellingson Benjamin M, Wen Patrick Y, van den Bent Martin J, Cloughesy Timothy F

机构信息

Department of Radiological Sciences (B.M.E.), Department of Biomedical Physics, David Geffen School of Medicine at UCLA (B.M.E.); Department of Bioengineering, Henry Samueli School of Engineering and Applied Science at UCLA (B.M.E.); Brain Research Institute, David Geffen School of Medicine at UCLA (B.M.E., T.F.C.); UCLA Neuro-Oncology Program, David Geffen School of Medicine at UCLA, Los Angeles, California (B.M.E., T.F.C.); Center for Neuro-Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, Massachusetts (P.Y.W.); Department of Neuro-Oncology, Erasmus MC Cancer Institute, Rotterdam, Netherlands (M.J.v.d.B.); Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, California (T.F.C.).

出版信息

Neuro Oncol. 2014 Oct;16 Suppl 7(Suppl 7):vii2-11. doi: 10.1093/neuonc/nou224.

DOI:10.1093/neuonc/nou224
PMID:25313235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4195528/
Abstract

Over the past 20 years, very few agents have been approved for the treatment of brain tumors. Recent studies have highlighted some of the challenges in assessing activity in novel agents for the treatment of brain tumors. This paper reviews some of the key challenges related to assessment of tumor response to therapy in adult high-grade gliomas and discusses the strengths and limitations of imaging-based endpoints. Although overall survival is considered the "gold standard" endpoint in the field of oncology, progression-free survival and response rate are endpoints that hold great value in neuro-oncology. Particular focus is given to advancements made since the January 2006 Brain Tumor Endpoints Workshop, including the development of Response Assessment in Neuro-Oncology criteria, the value of T2/fluid-attenuated inversion recovery, use of objective response rates and progression-free survival in clinical trials, and the evaluation of pseudoprogression, pseudoresponse, and inflammatory response in radiographic images.

摘要

在过去20年里,获批用于治疗脑肿瘤的药物极少。近期研究凸显了评估新型脑肿瘤治疗药物活性时面临的一些挑战。本文回顾了与评估成人高级别胶质瘤治疗后肿瘤反应相关的一些关键挑战,并讨论了基于成像的终点指标的优势与局限性。尽管总生存期被视为肿瘤学领域的“金标准”终点指标,但无进展生存期和缓解率在神经肿瘤学中也是具有重要价值的终点指标。本文特别关注自2006年1月脑肿瘤终点指标研讨会以来取得的进展,包括神经肿瘤学疗效评估标准的制定、T2加权/液体衰减反转恢复序列的价值、临床试验中客观缓解率和无进展生存期的应用,以及影像学图像中假性进展、假性缓解和炎症反应的评估。