Taal W, van der Rijt C D D, Sillevis Smitt P A E, Kros J M, van Heuvel I, Enting R H, van den Bent M J
Erasmus MC, locatie Daniel den Hoed Oncologisch Centrum, Postbus 5201, Rotterdam.
Ned Tijdschr Geneeskd. 2005 Jun 18;149(25):1393-9.
To describe the results of the treatment of recurrent glioma with temozolomide.
Retrospective.
This study evaluated 77 patients with a recurrent high-grade glioma who from August 1997-December 2003 were treated with temozolomide (150-200 mg/m2/day for 5 days per 28-day cycle) following surgery and radiotherapy at the Daniel den Hoed Oncology Centre of the Erasmus MC, Rotterdam, the Netherlands. The patients were divided into 4 groups depending on histology and chemotherapy history.
15 patients received temozolomide for a recurrent anaplastic oligodendroglioma or mixed oligo-astrocytoma. The response in this group was 80% and after 12 months in 47% of the patients there was no disease progression. 35 patients underwent second-line chemotherapy with temozolomide after earlier chemotherapy with procarbazine, lomustine and vincristine for recurrent anaplastic oligodendroglioma or mixed oligo-astrocytoma. Response was 26% and after 12 months in 15% of patients there was still no disease progression. 14 patients were treated with temozolomide for a recurrent anaplastic astrocytoma with a response of 35% and after 12 months in 8% of these patients there was no disease progression. Of the 13 patients with a recurrent glioblastoma who were treated with temozolomide 16% responded and after 6 and 12 months 21% were still free from progression. Temozolomide was well-tolerated: 2 patients had to stop because of probable side effects. CONCLUSION. Temozolomide has an acceptable safety profile and may be regarded as the preferred treatment for recurrent anaplastic gliomas after radiotherapy. There is only a limited role for temozolomide in the treatment of recurrent glioblastoma.
描述替莫唑胺治疗复发性胶质瘤的结果。
回顾性研究。
本研究评估了1997年8月至2003年12月期间在荷兰鹿特丹伊拉斯姆斯医学中心丹尼尔·登·霍德肿瘤中心接受手术和放疗后用替莫唑胺(每28天周期,150 - 200mg/m²/天,连用5天)治疗的77例复发性高级别胶质瘤患者。根据组织学和化疗史将患者分为4组。
15例患者接受替莫唑胺治疗复发性间变性少突胶质细胞瘤或混合性少突-星形细胞瘤。该组的缓解率为80%,12个月后47%的患者无疾病进展。35例患者在先前接受丙卡巴肼、洛莫司汀和长春新碱治疗复发性间变性少突胶质细胞瘤或混合性少突-星形细胞瘤后,接受替莫唑胺二线化疗。缓解率为26%,12个月后15%的患者仍无疾病进展。14例患者接受替莫唑胺治疗复发性间变性星形细胞瘤,缓解率为35%,12个月后8%的患者无疾病进展。13例复发性胶质母细胞瘤患者接受替莫唑胺治疗,缓解率为16%,6个月和12个月后21%的患者仍无进展。替莫唑胺耐受性良好:2例患者因可能的副作用不得不停药。结论。替莫唑胺具有可接受的安全性,可被视为放疗后复发性间变性胶质瘤的首选治疗方法。替莫唑胺在复发性胶质母细胞瘤的治疗中作用有限。