Jeremic B, Shibamoto Y, Gruijicic D, Milicic B, Stojanovic M, Nikolic N, Dagovic A, Aleksandrovic J
Department of Oncology, University Hospital, Kragujevac, Yugoslavia.
J Neurooncol. 1999 Jun;43(2):179-85. doi: 10.1023/a:1006206800947.
To investigate feasibility, toxicity and antitumor activity of combined surgery, postoperative radiation therapy (RT) and adjuvant chemotherapy (CHT) in adult patients with pure anaplastic oligodendroglioma (PAO) or mixed anaplastic oligoastrocytoma (MAO).
Between January 1988, and June 1993, 23 patients entered into a phase II study. After surgery, postoperative RT was administered with 60 Gy in 30 daily fractions in 30 treatment days in 6 weeks. Two weeks after RT, adjuvant 'modified' PCV (mPCV) (Procarbazine, 60 mg/m2, days 1-14; CCNU, 100 mg/m2, day 1; and vincristine, 1.4 mg/m2 (max. 2 mg), days 1 and 8) was administered every six weeks up to six cycles or until progression occurred.
Median survival time is not attained yet, while 1-5 year survival rates are 100%, 100%, 78%, 61%, and 52%, respectively. Median time to tumor progression is not attained yet, while 1-5 year progression-free survival rates are 100%, 100%, 70%, 52%, and 52%, respectively. On univariate analysis of potential prognostic factors, sex, tumor location (frontal versus other), and histology (pure versus mixed anaplastic oligodendroglioma) were not found to influence survival. Age of < 50 years carried improved prognosis as well as Karnofsky performance status (KPS) 90-100 when compared to KPS of 70-80. Patients having tumors < or = 4 cm did better than those with tumors > 4 cm as well as those with total tumor resection when compared to those with subtotal tumor resection or biopsy only. Acute high-grade (> or = 3) CHT-related toxicity was mainly hematological with only 3 (13%) patients experiencing acute grade 4 toxicity.
Combined treatment modality consisting of surgery, postoperative high-dose RT and mPCV chemotherapy for patients with anaplastic oligodendroglioma was effective with acceptable toxicity. Further studies are needed with more patients and longer follow-up to verify these results in this rare disease.
探讨手术、术后放疗(RT)及辅助化疗(CHT)联合治疗成人纯间变性少突胶质细胞瘤(PAO)或间变性少突-星形细胞瘤(MAO)的可行性、毒性及抗肿瘤活性。
1988年1月至1993年6月,23例患者进入II期研究。术后放疗,在6周内的30个治疗日给予60 Gy,每日1次,共30次分割。放疗后2周,每6周给予辅助“改良”PCV(mPCV)方案(甲基苄肼,60 mg/m²,第1 - 14天;洛莫司汀,100 mg/m²,第1天;长春新碱,1.4 mg/m²(最大2 mg),第1天和第8天),共6个周期或直至疾病进展。
中位生存时间尚未达到,1 - 5年生存率分别为100%、100%、78%、61%和52%。中位肿瘤进展时间尚未达到,1 - 5年无进展生存率分别为100%、100%、70%、52%和52%。对潜在预后因素进行单因素分析时,未发现性别、肿瘤位置(额叶与其他部位)及组织学类型(纯间变性少突胶质细胞瘤与混合型)对生存有影响。与KPS为70 - 80的患者相比,年龄<50岁以及Karnofsky功能状态(KPS)为90 - 100的患者预后较好。肿瘤≤4 cm的患者比肿瘤>4 cm的患者预后好,行肿瘤全切的患者比仅行次全切除或活检的患者预后好。急性重度(≥3级)CHT相关毒性主要为血液学毒性,仅3例(13%)患者出现急性4级毒性。
对于间变性少突胶质细胞瘤患者,手术、术后大剂量放疗及mPCV化疗的联合治疗方式有效,毒性可接受。需要更多患者及更长随访时间的进一步研究来验证这种罕见疾病的这些结果。