Urban C, Benesch M, Pakisch B, Lackner H, Kerbl R, Schwinger W, Oberbauer R
Division of Pediatric Hematology/Oncology, University Children's Hospital, University of Graz, Austria.
J Neurooncol. 1998 Aug;39(1):71-80. doi: 10.1023/a:1005966407408.
The prognosis of patients with incompletely resected malignant brain tumors is almost fatal. In an attempt to improve the outcome of children and young adults with unfavorable brain tumors an intensive multimodal therapeutic strategy was developed combining simultaneous (hyper)fractionated external beam irradiation and conventional adjuvant chemotherapy after initial surgery. 17 patients aged between 2.10 and 25.11 years were entered into the study. 16/17 patients were treated according to the German/Austrian Pediatric Brain Tumor Study Group multicenter trial HIT '91. They are not protocol patients of this HIT '91 trial. Induction chemotherapy consisted of 2 courses of ifosfamide (3 g/m2/d) on days 1-3, etoposide (150 mg/m2/d) on days 4-6, methotrexate (5 g/m2) on days 15 and 22, cisplatin (40 mg/m2/d) and cytarabine (400 mg/m2/d) on days 29-31. Three weeks after the last dose of cisplatin/cytarabine the second course of chemotherapy was started. The last patient entered into the study received a modified therapy containing ifosfamide, cisplatin and etoposide. Synchronously at a median of 12 days after initiation of chemotherapy 12/17 patients received local radiotherapy (6000-7040 cGy) to the brain and 5/17 patients craniospinal irradiation (3520 cGy with a tumor boost of 1400-2000 cGy). 4-6 weeks after completion of the second course of chemotherapy maintenance therapy was started with carmustine (CCNU) (75 mg/m2) and carboplatin (400 mg/m2) each on day 1 and vincristine (1.5 mg/m2) on day 1, 8, 15. This course was repeated eight times every six weeks. 9/17 patients are alive at a median follow-up of 25 months (range 5-50) with 4 complete remissions, 2 partial remissions and 1 stable disease lasting 42+ months. Two patients, who initially had stable disease, progressed, but are still alive at 31+ and 41+ months after diagnosis. Median progression-free survival and median overall survival is 19 and 36 months, respectively. Hematologic and methotrexate-induced toxicity were severe and resulted in one therapy-related death. However, radiotherapy concomitant to chemotherapy appears to be an effective method of treatment for brain tumors with poor prognosis, though toxicity is severe in some cases.
恶性脑肿瘤切除不完全的患者预后几乎是致命的。为了改善患有预后不良脑肿瘤的儿童和年轻人的治疗结果,制定了一种强化多模式治疗策略,在初始手术后同时进行(超)分割外照射和常规辅助化疗。17名年龄在2.10岁至25.11岁之间的患者进入该研究。16/17名患者按照德国/奥地利儿科脑肿瘤研究组多中心试验HIT '91进行治疗。他们不是该HIT '91试验的方案患者。诱导化疗包括在第1 - 3天使用2个疗程的异环磷酰胺(3 g/m²/天)、在第4 - 6天使用依托泊苷(150 mg/m²/天)、在第15天和第22天使用甲氨蝶呤(5 g/m²)、在第29 - 31天使用顺铂(40 mg/m²/天)和阿糖胞苷(400 mg/m²/天)。在最后一剂顺铂/阿糖胞苷给药三周后开始第二个化疗疗程。最后一名进入该研究的患者接受了包含异环磷酰胺、顺铂和依托泊苷的改良疗法。同步地,在化疗开始后的中位12天,12/17名患者接受了脑部局部放疗(6000 - 7040 cGy),5/17名患者接受了全脑脊髓放疗(3520 cGy,肿瘤部位加量1400 - 2000 cGy)。在完成第二个化疗疗程后的4 - 6周,开始维持治疗,在第1天使用卡莫司汀(CCNU)(75 mg/m²)和卡铂(400 mg/m²),在第1、8、15天使用长春新碱(1.5 mg/m²)。这个疗程每六周重复八次。9/17名患者在中位随访25个月(范围5 - 50个月)时存活,其中4例完全缓解,2例部分缓解,1例疾病稳定持续42 +个月。两名最初疾病稳定的患者病情进展,但在诊断后31 +和41 +个月时仍存活。无进展生存期和总生存期的中位数分别为19个月和36个月。血液学毒性和甲氨蝶呤诱导的毒性严重,导致1例与治疗相关的死亡。然而,化疗同步放疗似乎是治疗预后不良脑肿瘤的一种有效方法,尽管在某些情况下毒性严重。