切除的间变性少突胶质细胞瘤患者联合放疗和联合化疗
丙卡巴嗪、CCNU 和长春新碱化疗辅助治疗高度间变性少突胶质细胞瘤患者的 III 期研究
基本原理:放射疗法使用高能 X 射线破坏肿瘤细胞,可能是间变性少突胶质细胞瘤的有效治疗方法。 将联合化疗与放疗相结合可能会杀死更多的肿瘤细胞。
目的:随机 III 期试验,比较放疗联合和不联合化疗对切除的间变性少突胶质细胞瘤患者的疗效。
研究概览
详细说明
目标:I. 比较间变性少突胶质细胞瘤患者在手术切除后接受放疗联合或不联合丙卡巴肼、洛莫司汀和长春新碱 (PCV) 辅助治疗的生存期和首次进展时间。 二。 调查 PCV 对这些患者生活质量和神经功能的影响。 三、 确定 PCV 在这些患者中的毒性。 四、 将染色体病变(1p 和/或 19q、9p、p53 丢失和突变、7 号染色体扩增或 10 号染色体丢失)与接受这些方案治疗的患者的无进展生存期和总生存期相关联。
大纲:这是一项随机、多中心研究。 根据年龄、切除范围、体能状态、既往手术史和参与中心对患者进行分层。 患者被随机分配到两个治疗组之一。 第 I 组:在手术后 4-6 周内,患者接受超过 7 周的放疗以达到残留的肿瘤体积。 第二组:患者接受与第一组相同的放疗,然后在放疗完成后 4 周内开始化疗。 患者在第 1 天接受口服洛莫司汀,在第 8-21 天接受口服丙卡巴肼,在第 8 天和第 29 天接受长春新碱静脉注射。 在稳定和有反应的患者中每 6 周重复一次治疗,总共 6 个疗程。 疾病复发的患者可以接受 6 个额外的化疗疗程,如上或研究者决定的另一种方式。 患者每 3 个月随访 1 年,然后每 6 个月随访一次以观察生存情况。
预计应计:在 4 年内,这项研究将总共招募 350 名患者。
研究类型
注册 (预期的)
阶段
- 第三阶段
联系人和位置
学习地点
-
-
-
Budapest、匈牙利、1145
- National Institute of Neurosurgery
-
-
-
-
-
Vienna (Wien)、奥地利、A-1100
- Kaiser Franz Josef Hospital
-
-
-
-
-
Hannover、德国、D-30559
- Neurologische Klinik der Henriettenstiftung
-
Jena、德国、D-07740
- Klinikum der Friedrich-Schiller Universitaet Jena
-
-
-
-
-
Padova、意大利、35128
- Universita Di Padova
-
Padova (Padua)、意大利、35128
- Azienda Ospedaliera di Padova
-
-
-
-
-
Brussels、比利时、1070
- Hopital Universitaire Erasme
-
Brussels (Bruxelles)、比利时、1090
- Academisch Ziekenhuis der Vrije Universiteit Brussel
-
Haine Saint Paul、比利时、7100
- Hopital De Jolimont
-
Leuven、比利时、B-3000
- U.Z. Gasthuisberg
-
-
-
-
-
Lille、法国、59037
- Centre Hospitalier Regional de Lille
-
Marseille、法国、13385
- CHU de la Timone
-
Nancy、法国、54035
- CHU de Nancy - Hopital Neurologique
-
Nantes-Saint Herblain、法国、44805
- CRLCC Nantes - Atlantique
-
Nice、法国、06189
- Centre Antoine Lacassagne
-
Nice、法国、06002
- Hôpital Pasteur
-
Nimes、法国、30000
- C.H.R. de Nimes - Hopital Caremeau
-
Paris、法国、75651
- CHU Pitié-Salpétrière
-
Rennes、法国、35064
- Centre Eugene Marquis
-
Villejuif、法国、F-94805
- Institut Gustave Roussy
-
-
-
-
-
Linkoping、瑞典、S-581 85
- University Hospital of Linkoping
-
Umea、瑞典、S-901 85
- Umeå universitet
-
-
-
-
-
Lausanne、瑞士、CH-1011
- Centre Hospitalier Universitaire Vaudois
-
-
-
-
-
Turku、芬兰、FIN-2-0521
- Turku University Central Hospital
-
-
-
-
England
-
Nottingham、England、英国、NG7 2UH
- Queen's Medical Centre
-
Nottingham、England、英国、NG5 1PB
- Nottingham City Hospital NHS Trust
-
Nottingham、England、英国、NG1 6HA
- Nottingham General Hospital
-
Southampton、England、英国、SO16 6YD
- Southampton General Hospital
-
Southampton、England、英国、SO14 0YG
- Royal South Hants Hospital
-
Sutton、England、英国、SM2 5PT
- Royal Marsden Hospital
-
-
-
-
-
's-Gravenhage (Den Haag, The Hague)、荷兰、2501 CK
- Medisch Centrum Haaglanden
-
Amsterdam、荷兰、1105 AZ
- Academisch Medisch Centrum
-
Amsterdam、荷兰、1001HV
- Vrije Universiteit Medisch Centrum
-
Groningen、荷兰、9713 EZ
- Academisch Ziekenhuis Groningen
-
Nijmegen、荷兰、NL-6500 HB
- University Medical Center Nijmegen
-
Rotterdam、荷兰、3075 EA
- Rotterdam Cancer Institute
-
Tilburg、荷兰、5022 GC
- St. Elisabeth Ziekenhuis
-
Tilburg、荷兰、5042 SB
- Dr. Bernard Verbeeten Instituut
-
Utrecht、荷兰、3584 CX
- Academisch Ziekenhuis Utrecht
-
-
-
-
-
Lisbon、葡萄牙、1093
- Instituto Portugues de Oncologia de Francisco Gentil
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
疾病特征: 新诊断的少突胶质细胞瘤或少突星形细胞瘤(具有至少 25% 的少突胶质成分) 低级别少突星形细胞瘤或少突胶质细胞瘤在未经放疗的手术后复发是允许的选项)需要 至少具有以下组织学间变性特征中的 3 种: 高细胞结构 内皮异常 核异常 坏死 有丝分裂
患者特征: 年龄:16 至 69 岁 体能状态:ECOG 0-2 预期寿命:至少 3 个月 造血:WBC 至少 3,000/mm3 血小板计数至少 100,000/mm3 肝脏:胆红素不超过 1.4 mg/dL 肾脏:肌酐不超过 1.3 mg/dL 肌酐清除率至少 60 mL/min 其他:未怀孕或哺乳 可生育患者必须使用有效的避孕措施 无活动性或不受控制的感染 无其他会妨碍研究的疾病,包括恶性肿瘤 无会影响研究的神经或精神障碍排除研究
先前同时进行的治疗: 生物疗法:未指定 化学疗法:未先前化学疗法 内分泌疗法:未指定 放射疗法:见疾病特征
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
合作者和调查者
出版物和有用的链接
一般刊物
- Idbaih A, Dalmasso C, Kouwenhoven M, Jeuken J, Carpentier C, Gorlia T, Kros JM, French P, Teepen J, Broet P, Delattre O, Mokhtari K, Sanson M, Delattre JY, van den Bent M, Hoang-Xuan K. Genomic aberrations associated with outcome in anaplastic oligodendroglial tumors treated within the EORTC phase III trial 26951. J Neurooncol. 2011 Jun;103(2):221-30. doi: 10.1007/s11060-010-0380-9. Epub 2010 Sep 6.
- Mokhtari K, Ducray F, Kros JM, Gorlia T, Idbaih A, Taphoorn M, Wesseling P, Hoang-Xuan K, Van den Bent M, Sanson M. Alpha-internexin expression predicts outcome in anaplastic oligodendroglial tumors and may positively impact the efficacy of chemotherapy: European organization for research and treatment of cancer trial 26951. Cancer. 2011 Jul 1;117(13):3014-26. doi: 10.1002/cncr.25827. Epub 2011 Jan 18.
- van den Bent MJ, Gravendeel LA, Gorlia T, Kros JM, Lapre L, Wesseling P, Teepen JL, Idbaih A, Sanson M, Smitt PA, French PJ. A hypermethylated phenotype is a better predictor of survival than MGMT methylation in anaplastic oligodendroglial brain tumors: a report from EORTC study 26951. Clin Cancer Res. 2011 Nov 15;17(22):7148-55. doi: 10.1158/1078-0432.CCR-11-1274. Epub 2011 Sep 13.
- Preusser M, Hoeftberger R, Woehrer A, et al.: Prognostic value and analytical performance (reproducibility) of Ki67 index in anaplastic oligodendroglial tumors: A translational study of the EORTC Brain Tumor Group. [Abstract] J Clin Oncol 28 (Suppl 15): A-2029, 2010.
- van den Bent MJ, Dubbink HJ, Marie Y, Brandes AA, Taphoorn MJ, Wesseling P, Frenay M, Tijssen CC, Lacombe D, Idbaih A, van Marion R, Kros JM, Dinjens WN, Gorlia T, Sanson M. IDH1 and IDH2 mutations are prognostic but not predictive for outcome in anaplastic oligodendroglial tumors: a report of the European Organization for Research and Treatment of Cancer Brain Tumor Group. Clin Cancer Res. 2010 Mar 1;16(5):1597-604. doi: 10.1158/1078-0432.CCR-09-2902. Epub 2010 Feb 16.
- Kouwenhoven MC, Gorlia T, Kros JM, Ibdaih A, Brandes AA, Bromberg JE, Mokhtari K, van Duinen SG, Teepen JL, Wesseling P, Vandenbos F, Grisold W, Sipos L, Mirimanoff R, Vecht CJ, Allgeier A, Lacombe D, van den Bent MJ. Molecular analysis of anaplastic oligodendroglial tumors in a prospective randomized study: A report from EORTC study 26951. Neuro Oncol. 2009 Dec;11(6):737-46. doi: 10.1215/15228517-2009-011.
- van den Bent MJ, Dubbink HJ, Sanson M, van der Lee-Haarloo CR, Hegi M, Jeuken JW, Ibdaih A, Brandes AA, Taphoorn MJ, Frenay M, Lacombe D, Gorlia T, Dinjens WN, Kros JM. MGMT promoter methylation is prognostic but not predictive for outcome to adjuvant PCV chemotherapy in anaplastic oligodendroglial tumors: a report from EORTC Brain Tumor Group Study 26951. J Clin Oncol. 2009 Dec 10;27(35):5881-6. doi: 10.1200/JCO.2009.24.1034. Epub 2009 Nov 9.
- Kros JM, Gorlia T, Kouwenhoven MC, Zheng PP, Collins VP, Figarella-Branger D, Giangaspero F, Giannini C, Mokhtari K, Mork SJ, Paetau A, Reifenberger G, van den Bent MJ. Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951: assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome. J Neuropathol Exp Neurol. 2007 Jun;66(6):545-51. doi: 10.1097/01.jnen.0000263869.84188.72.
- Mauer ME, Taphoorn MJ, Bottomley A, Coens C, Efficace F, Sanson M, Brandes AA, van der Rijt CC, Bernsen HJ, Frenay M, Tijssen CC, Lacombe D, van den Bent MJ; EORTC Brain Cancer Group. Prognostic value of health-related quality-of-life data in predicting survival in patients with anaplastic oligodendrogliomas, from a phase III EORTC brain cancer group study. J Clin Oncol. 2007 Dec 20;25(36):5731-7. doi: 10.1200/JCO.2007.11.1476.
- Taphoorn MJ, van den Bent MJ, Mauer ME, Coens C, Delattre JY, Brandes AA, Sillevis Smitt PA, Bernsen HJ, Frenay M, Tijssen CC, Lacombe D, Allgeier A, Bottomley A; European Organisation for Research and Treatment of Cancer. Health-related quality of life in patients treated for anaplastic oligodendroglioma with adjuvant chemotherapy: results of a European Organisation for Research and Treatment of Cancer randomized clinical trial. J Clin Oncol. 2007 Dec 20;25(36):5723-30. doi: 10.1200/JCO.2007.12.7514.
- van den Bent MJ, Carpentier AF, Brandes AA, Sanson M, Taphoorn MJ, Bernsen HJ, Frenay M, Tijssen CC, Grisold W, Sipos L, Haaxma-Reiche H, Kros JM, van Kouwenhoven MC, Vecht CJ, Allgeier A, Lacombe D, Gorlia T. Adjuvant procarbazine, lomustine, and vincristine improves progression-free survival but not overall survival in newly diagnosed anaplastic oligodendrogliomas and oligoastrocytomas: a randomized European Organisation for Research and Treatment of Cancer phase III trial. J Clin Oncol. 2006 Jun 20;24(18):2715-22. doi: 10.1200/JCO.2005.04.6078.
- van den Bent MJ, Delattre JY, Brandes AA, et al.: First analysis of EORTC trial 26951, a randomized phase III study of adjuvant PCV chemotherapy in patients with highly anaplastic oligodendroglioma. [Abstract] J Clin Oncol 23 (Suppl 16): A-1503, 114s, 2005.
- Lassman AB, Hoang-Xuan K, Polley MC, Brandes AA, Cairncross JG, Kros JM, Ashby LS, Taphoorn MJB, Souhami L, Dinjens WNM, Laack NN, Kouwenhoven MCM, Fink KL, French PJ, Macdonald DR, Lacombe D, Won M, Gorlia T, Mehta MP, van den Bent MJ. Joint Final Report of EORTC 26951 and RTOG 9402: Phase III Trials With Procarbazine, Lomustine, and Vincristine Chemotherapy for Anaplastic Oligodendroglial Tumors. J Clin Oncol. 2022 Aug 10;40(23):2539-2545. doi: 10.1200/JCO.21.02543. Epub 2022 Jun 22.
- Erdem-Eraslan L, Gravendeel LA, de Rooi J, Eilers PH, Idbaih A, Spliet WG, den Dunnen WF, Teepen JL, Wesseling P, Sillevis Smitt PA, Kros JM, Gorlia T, van den Bent MJ, French PJ. Intrinsic molecular subtypes of glioma are prognostic and predict benefit from adjuvant procarbazine, lomustine, and vincristine chemotherapy in combination with other prognostic factors in anaplastic oligodendroglial brain tumors: a report from EORTC study 26951. J Clin Oncol. 2013 Jan 20;31(3):328-36. doi: 10.1200/JCO.2012.44.1444. Epub 2012 Dec 26.
- van den Bent MJ, Brandes AA, Taphoorn MJ, Kros JM, Kouwenhoven MC, Delattre JY, Bernsen HJ, Frenay M, Tijssen CC, Grisold W, Sipos L, Enting RH, French PJ, Dinjens WN, Vecht CJ, Allgeier A, Lacombe D, Gorlia T, Hoang-Xuan K. Adjuvant procarbazine, lomustine, and vincristine chemotherapy in newly diagnosed anaplastic oligodendroglioma: long-term follow-up of EORTC brain tumor group study 26951. J Clin Oncol. 2013 Jan 20;31(3):344-50. doi: 10.1200/JCO.2012.43.2229. Epub 2012 Oct 15.
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.