Janny P, Cure H, Mohr M, Heldt N, Kwiatkowski F, Lemaire J J, Plagne R, Rozan R
Department of Neurosurgery, Hôpital Fontmaure, Chalmalières, France.
Cancer. 1994 Apr 1;73(7):1937-45. doi: 10.1002/1097-0142(19940401)73:7<1937::aid-cncr2820730727>3.0.co;2-g.
The authors examined the principal prognostic factors for supratentorial low grade astrocytomas and the effects of treatment on survival time.
Fifty-eight patients, 32 males and 26 females, treated from January 1970 through December 1990 are reported. Thirty-five patients underwent surgery, of whom three died. Among the survivors there were 7 gross total resections, 13 subtotal resections, and 12 partial resections. Of the 23 remaining patients, diagnosis was obtained by stereotactic biopsy. Twenty-five patients were irradiated and eight received chemotherapy. The histologic material, originally graded 1 or 2 according to Kernohan's system, was reviewed using the St. Anne-Mayo Clinic system, with which there were 18 Grade 3 tumors.
Six patients had pilocytic astrocytomas (mean age, 18 years), of which three astrocytomas could be removed, and the patients were well 128, 152, and 254 months, respectively, after diagnosis. Among the other three patients, one with a hypothalamic localization refused any form of treatment and died rapidly. The remaining two patients also had deep-seated tumors and were irradiated: one died 17 months later, and the other remained relapse free 56 months after diagnosis. The 49 patients with ordinary astrocytomas who survived surgery (mean age, 37 years) had a median survival time of 64 months and 5- and 10-year survival rates of 54.6% and 34.1%, respectively. Patients with Grade 1 or 2 tumors had a median survival time of 108.6 months, compared with 39.4 months for patients with Grade 3 tumors. Gross total and subtotal resections were significantly associated with longer survival time only in patients with Grade 1 and 2 tumors: in this group, the 5- and 10-year survival rates were 87.5% and 68.2%, respectively, when tumor was completely resected, instead of 57% and 31.2% in patients with incomplete or no surgical resection. There was a trend suggesting that antimitotic drugs and X-ray therapy could benefit patients with Grade 3 tumors.
The importance of an accurate histologic grading system and a gross total resection of Grade 1 and 2 astrocytomas is emphasized.
作者研究了幕上低级别星形细胞瘤的主要预后因素以及治疗对生存时间的影响。
报告了1970年1月至1990年12月期间治疗的58例患者,其中男性32例,女性26例。35例患者接受了手术,其中3例死亡。在幸存者中,7例肿瘤全切,13例次全切,12例部分切除。其余23例患者通过立体定向活检确诊。25例患者接受了放疗,8例接受了化疗。根据圣安妮-梅奥诊所系统对最初按照克诺汉系统分级为1级或2级的组织学材料进行重新评估,其中有18例3级肿瘤。
6例患者为毛细胞型星形细胞瘤(平均年龄18岁),其中3例肿瘤可切除,诊断后分别在128、152和254个月时情况良好。在其他3例患者中,1例位于下丘脑的患者拒绝任何形式的治疗并很快死亡。其余2例患者也有深部肿瘤并接受了放疗:1例在17个月后死亡,另1例在诊断后56个月无复发。49例手术存活的普通星形细胞瘤患者(平均年龄37岁)的中位生存时间为64个月,5年和10年生存率分别为54.6%和34.1%。1级或2级肿瘤患者的中位生存时间为108.6个月,而3级肿瘤患者为39.4个月。仅在1级和2级肿瘤患者中,肿瘤全切和次全切与更长的生存时间显著相关:在该组中,肿瘤完全切除时5年和10年生存率分别为87.5%和68.2%,而不完全切除或未手术切除的患者分别为57%和31.2%。有趋势表明抗有丝分裂药物和X线治疗可能使3级肿瘤患者受益。
强调了准确的组织学分级系统以及1级和2级星形细胞瘤全切的重要性。