Henriksson Roger, Malmström Annika, Bergström Per, Bergh Gertrud, Trojanowski Thomas, Andreasson Lars, Blomquist Erik, Jonsborg Sonny, Edekling Tomas, Salander Pär, Brännström Thomas, Bergenheim A Tommy
Department of Radiation Sciences and Oncology, Umeå University Hospital, Umeå, Sweden.
J Neurooncol. 2006 Jul;78(3):321-6. doi: 10.1007/s11060-005-9106-9. Epub 2006 Apr 6.
Experimental and early clinical investigations have demonstrated encouraging results for estramustine in the treatment of malignant glioma. The present study is an open randomized clinical trial comparing estramustine phosphate (Estracyt) in addition to radiotherapy with radiotherapy alone as first line treatment of astrocytoma grade III and IV. The 140 patients included were in a good clinical condition with a median age of 55 years (range 22-87). Estramustine was given orally, 280 mg twice daily, as soon as the diagnosis was established, during and after the radiotherapy for a period of in total 3 months. Radiotherapy was delivered on weekdays 2 Gy daily up to 56 Gy. Eighteen patients were excluded due to misclassification, leaving 122 patients eligible for evaluation. Overall the treatment was well tolerated. Mild or moderate nausea was the most common side effect of estramustine. The minimum follow-up time was 5.2 years for the surviving patients. For astrocytoma grade III the median survival time was 10.6 (1.3-92.7) months for the radiotherapy only group and 17.3 (0.4-96.9+) months for the estramustine + radiotherapy group. In grade IV the corresponding median survival time was 12.3 (2.1-89.2) and 10.3 (0.3-91.7+) months, respectively. Median time to progress for radiotherapy only and radiotherapy and estramustin group in grade III tumours was 6.5 and 10.1 months, respectively. In grade IV tumours the corresponding figures were 5.1 and 3.3 months, respectively. Although there was a tendency for improved survival in grade III, no statistical significant differences were found between the treatment groups. No differences between the two treatment groups were evident with respect to quality of life according to the EORTC QLQ-protocol. In conclusion, this first randomized study did not demonstrate any significant improvement of using estramustine in addition to conventional radiotherapy, however, a trend for a positive response for the estramustine group was found in patients with grade III glioma.
实验性研究和早期临床调查表明,雌莫司汀治疗恶性胶质瘤的效果令人鼓舞。本研究是一项开放随机临床试验,比较磷酸雌莫司汀(癌腺治)联合放疗与单纯放疗作为Ⅲ级和Ⅳ级星形细胞瘤一线治疗的效果。纳入的140例患者临床状况良好,中位年龄55岁(范围22 - 87岁)。一旦确诊,在放疗期间及放疗后共3个月内,口服雌莫司汀,每日2次,每次280mg。放疗在工作日进行,每日2Gy,总量达56Gy。18例患者因分类错误被排除,剩余122例患者符合评估条件。总体而言,治疗耐受性良好。轻度或中度恶心是雌莫司汀最常见的副作用。存活患者的最短随访时间为5.2年。对于Ⅲ级星形细胞瘤,单纯放疗组的中位生存时间为10.6(1.3 - 92.7)个月,雌莫司汀 + 放疗组为17.3(0.4 - 96.9 +)个月。在Ⅳ级中,相应的中位生存时间分别为12.3(2.1 - 89.2)和10.3(0.3 - 91.7 +)个月。Ⅲ级肿瘤中,单纯放疗组和放疗加雌莫司汀组的中位进展时间分别为6.5个月和10.1个月。在Ⅳ级肿瘤中,相应数字分别为5.1个月和3.3个月。尽管Ⅲ级患者有生存改善的趋势,但治疗组之间未发现统计学显著差异。根据欧洲癌症研究与治疗组织(EORTC)QLQ方案,两个治疗组在生活质量方面没有明显差异。总之,这项首次随机研究未显示在传统放疗基础上加用雌莫司汀有任何显著改善,然而,在Ⅲ级胶质瘤患者中发现雌莫司汀组有阳性反应的趋势。