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伴有少突胶质细胞成分的多形性胶质母细胞瘤(GBMO):术后接受放疗以及尼莫司汀(ACNU)和替尼泊苷(VM26)化疗后的良好预后。

Glioblastoma multiforme with oligodendroglial component (GBMO): favorable outcome after post-operative radiotherapy and chemotherapy with nimustine (ACNU) and teniposide (VM26).

作者信息

Vordermark Dirk, Ruprecht Klemens, Rieckmann Peter, Roggendorf Wolfgang, Vince Giles H, Warmuth-Metz Monika, Kölbl Oliver, Flentje Michael

机构信息

Dept. of Radiation Oncology, University of Würzburg, Würzburg, Germany.

出版信息

BMC Cancer. 2006 Oct 18;6:247. doi: 10.1186/1471-2407-6-247.

Abstract

BACKGROUND

The presence of an oligodendroglial component within a glioblastoma multiforme (GBM) is considered a prognostically favorable factor, but the clinical outcome of patients with glioblastoma multiforme with oligodendroglial component (GBMO) after combined post-operative radiotherapy and chemotherapy has rarely been reported.

METHODS

We analyzed overall and progression-free survival in a group of ten consecutive patients initially diagnosed with GBMO between 1996 and 2004 (4.2% of all GBM patients). Median (range) age was 54 (34-73) years, 90% were resected and median radiotherapy dose was 54 (45-60.6) Gy. 80% of patients received post-operative chemotherapy with nimustine (ACNU) and VM26 (teniposide) for a median of 3.5 (1-6) cycles, the remainder were treated with post-operative radiotherapy alone. All specimens were reviewed by an experienced neuropathologist.

RESULTS

Neuropathological re-evaluation revealed GBM with an oligodendroglial component of 30% or less in five cases, predominant oligoastrocytic tumors with focal areas of GBM in four patients and WHO grade III oligoastrocytoma with questionable transition to GBM in one patient. Four of ten patients were alive at at 40, 41, 41 and 82 months. The median overall survival (Kaplan-Meier) was 26 months, the 2-year survival rate was 60% (progression-free survival: 9.8 months and 40%, respectively).

CONCLUSION

In conclusion, patients with GBMO treated with post-operative radiotherapy and chemotherapy with ACNU/VM26 had a better prognosis than reported for GBM in modern chemoradiation series.

摘要

背景

多形性胶质母细胞瘤(GBM)中存在少突胶质细胞成分被认为是一个预后良好的因素,但关于多形性胶质母细胞瘤伴少突胶质细胞成分(GBMO)患者术后联合放疗和化疗后的临床结果鲜有报道。

方法

我们分析了1996年至2004年间连续诊断为GBMO的一组10例患者的总生存期和无进展生存期(占所有GBM患者的4.2%)。中位(范围)年龄为54(34 - 73)岁,90%的患者接受了手术切除,中位放疗剂量为54(45 - 60.6)Gy。80%的患者术后接受了尼莫司汀(ACNU)和VM26(替尼泊苷)化疗,中位疗程为3.5(1 - 6)个周期,其余患者仅接受术后放疗。所有标本均由经验丰富的神经病理学家复查。

结果

神经病理学重新评估显示,5例患者的GBM少突胶质细胞成分占30%或更少,4例患者为主要的少突星形细胞瘤伴GBM局灶区域,1例患者为世界卫生组织III级少突星形细胞瘤,有向GBM转变的可疑情况。10例患者中有4例分别在40、41、41和82个月时存活。中位总生存期(Kaplan - Meier法)为26个月,2年生存率为60%(无进展生存期分别为9.8个月和40%)。

结论

总之,接受术后放疗及ACNU/VM26化疗的GBMO患者的预后比现代放化疗系列报道的GBM患者更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ac/1621074/9b851a12430d/1471-2407-6-247-1.jpg

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