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高剂量他莫昔芬治疗会增加胶质母细胞瘤患者多灶性肿瘤复发的发生率。

High-dose tamoxifen treatment increases the incidence of multifocal tumor recurrences in glioblastoma patients.

作者信息

Puchner Maximilian J A, Giese Alf, Lohmann Frauke, Cristante Loris

机构信息

Department of Neurosurgery, Gilead Hospital, Bielefeld, Germany.

出版信息

Anticancer Res. 2004 Nov-Dec;24(6):4195-203.

Abstract

BACKGROUND

Multifocal tumor recurrences in glioblastoma patients are described in 4% - 14% of cases. Two recent studies, treating newly diagnosed glioblastoma patients with continuous high-dose tamoxifen (TAM), reported an increased incidence of multifocal tumor recurrences in 45.5% and 33% of study patients.

PATIENTS AND METHODS

Fifty newly diagnosed patients with glioblastoma were treated with 3 cycles of carboplatin, continuous high-dose TAM and radiotherapy. Tumor progression was determined on follow-up MRI studies at 3-month intervals and categorized as either local or multifocal.

RESULTS

Multifocal tumor recurrence was found in 16 (33%) out of 49 study patients. Compared to tumors which remained local, multifocal tumor recurrences were characterized by a significantly longer median time to tumor progression (41 vs. 23 weeks, Breslow test: p = 0.0123). Multifocal tumor recurrences were mainly observed after an initial response to the study treatment (81%), whereas local regrowth was more often associated with initial treatment failure, i.e. progressive disease (64%).

CONCLUSION

The association of the pattern of tumor recurrence with the type of response to TAM treatment suggests that acquired resistance to TAM might be an important contributing mechanism in the development of multifocal glioblastoma disease.

摘要

背景

胶质母细胞瘤患者中多灶性肿瘤复发的病例占4% - 14%。最近的两项研究对新诊断的胶质母细胞瘤患者采用连续高剂量他莫昔芬(TAM)进行治疗,报告显示研究患者中多灶性肿瘤复发的发生率分别为45.5%和33%。

患者与方法

五十名新诊断的胶质母细胞瘤患者接受了3个周期的卡铂、连续高剂量TAM及放疗治疗。每隔3个月通过随访MRI研究确定肿瘤进展情况,并将其分类为局部或多灶性。

结果

49名研究患者中有16名(33%)出现多灶性肿瘤复发。与仍为局部性的肿瘤相比,多灶性肿瘤复发的特征是肿瘤进展的中位时间显著更长(41周对23周,Breslow检验:p = 0.0123)。多灶性肿瘤复发主要在对研究治疗产生初始反应后出现(81%),而局部肿瘤再生长更常与初始治疗失败即疾病进展相关(64%)。

结论

肿瘤复发模式与对TAM治疗反应类型之间的关联表明,对TAM获得性耐药可能是多灶性胶质母细胞瘤疾病发生发展的一个重要促成机制。

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