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替莫唑胺为基础的放化疗后胶质母细胞瘤复发的模式和时间。

Patterns and timing of recurrence after temozolomide-based chemoradiation for glioblastoma.

机构信息

Department of Radiation Oncology, University of Rochester Medical Center, Rochester, NY 14642, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2010 Nov 15;78(4):1147-55. doi: 10.1016/j.ijrobp.2009.09.018. Epub 2010 Mar 6.

Abstract

PURPOSE

To determine recurrence patterns of glioblastoma treated with temozolomide-based chemoradiation.

METHODS

Pretreatment and serial posttreatment magnetic resonance imaging scans of 54 patients were retrospectively evaluated. Central recurrence (i.e., local progression) and the development of new (i.e., interval appearance of discrete enhancing lesion) in-field, marginal, and distant recurrences were assessed, with the pattern of recurrence of individual lesions defined relative to the 95% isodose line (D(95)). Distant recurrences were defined as lesions completely outside D(95), marginal recurrences crossed D(95), and in-field recurrences were completely inside D(95).

RESULTS

At a median follow-up of 17 months, 39 of 54 (72%) patients developed recurrent glioblastoma. Among these 39 patients, central recurrence occurred in 80% (at a median of 7 months from diagnosis); new in-field recurrence developed in 33% (at a median of 14 months); marginal recurrences developed in 15% (at a median of 18 months); and distant recurrences developed in 20% (at a median of 11 months). The actuarial rates of central, new in-field, marginal, distant, and any new recurrences at 1-year were 46%, 15%, 3%, 14%, and 25% respectively, whereas at 2 years, the rates were 68%, 60%, 32%, 28%, and 66%, reflecting an increasing probability of new lesions developing at later time points. Ten patients developed subependymal recurrences, of whom 7 developed multiple subependymal lesions.

CONCLUSIONS

Whereas central recurrence of glioblastoma treated with radiation and temozolomide predominates and persists over time, new in-field, marginal, and distant recurrences commonly develop, particularly at later time points in patients with longer survival.

摘要

目的

确定接受替莫唑胺为基础的放化疗治疗的胶质母细胞瘤的复发模式。

方法

回顾性评估了 54 例患者的预处理和连续治疗后磁共振成像扫描。评估了中央复发(即局部进展)和新出现的(即离散增强病变的间隔出现)场内、边缘和远处复发,并根据个体病变相对于 95%等剂量线(D(95))的复发模式来定义。远处复发定义为完全位于 D(95)之外的病变,边缘复发跨越 D(95),场内复发完全位于 D(95)内。

结果

在中位数为 17 个月的随访中,54 例患者中有 39 例(72%)发生了复发性胶质母细胞瘤。在这 39 例患者中,中央复发发生在 80%(从诊断到中位时间为 7 个月);新的场内复发发生在 33%(中位时间为 14 个月);边缘复发发生在 15%(中位时间为 18 个月);远处复发发生在 20%(中位时间为 11 个月)。1 年时中央、新场内、边缘、远处和任何新复发的累积发生率分别为 46%、15%、3%、14%和 25%,而 2 年时的发生率分别为 68%、60%、32%、28%和 66%,反映了新病变在以后时间点出现的可能性增加。10 例患者发生室管膜下复发,其中 7 例发生多个室管膜下病变。

结论

接受放疗和替莫唑胺治疗的胶质母细胞瘤中,中央复发占主导地位且随着时间的推移持续存在,而新的场内、边缘和远处复发通常会发生,尤其是在生存时间较长的患者中。

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