Calaminus G, Bamberg M, Harms D, Jürgens H, Kortmann R D, Sörensen N, Wiestler O D, Göbel U
Department of Pediatric Hematology and Oncology Children's Hospital, Heinrich Heine University Medical Center, University of Düsseldorf, Düsseldorf, Germany.
Neuropediatrics. 2005 Apr;36(2):71-7. doi: 10.1055/s-2005-837582.
The aim of the present study was to evaluate survival and factors influencing long-term outcome of patients with AFP/beta-HCG secreting (non-seminomatous) central nervous system germ cell tumors (secCNSGCT), who were prospectively collected in the cooperative MAKEI (German: maligne Keimzelltumoren) 89 protocol.
Between January 1989 and January 1994, 28 patients with secCNS GCT were registered and treated according to the MAKEI 89 protocol. The protocol recommended, after a clinically or histologically proven diagnosis and cisplatin-based chemotherapy, a resection of residual tumor and craniospinal irradiation (30 Gy) with a tumor boost (20 Gy).
The estimated (Kaplan-Meier) event-free survival (EFS) of protocol patients is 0.57 +/- 0.09 (n = 28) and the relapse-free survival (RFS) is 0.67 +/- 0.10 (at five and ten years). With respect to long-term survival, the combination of marked neurological symptoms at diagnosis along with primary tumor resection seem to be the main negative prognostic risk factors (Fisher exact test p < 0.05). CNS dissemination at diagnosis can also be considered as a negative risk factor as 3 of 5 patients with primary dissemination died of the disease.
Cisplatin-based three agent chemotherapy followed by resection of the residual tumor and craniospinal irradiation (CSI) with tumor boost is a successful and well-tolerated treatment for secCNSGCTs. The possibility of a clinical diagnosis based on MRI and tumor markers together with the use of modern neurosurgical techniques gives us the chance to postpone or even avoid major surgery. This gives an additional chance to reduce acute morbidity and further decrease late effects.
本研究旨在评估分泌甲胎蛋白/β-人绒毛膜促性腺激素(非精原细胞瘤)的中枢神经系统生殖细胞肿瘤(secCNSGCT)患者的生存率及影响长期预后的因素,这些患者是按照合作的MAKEI(德语:恶性生殖细胞肿瘤)89方案前瞻性收集的。
1989年1月至1994年1月期间,28例secCNS GCT患者登记并按照MAKEI 89方案进行治疗。该方案建议,在临床或组织学确诊并进行以顺铂为基础的化疗后,切除残留肿瘤并进行全脑全脊髓照射(30 Gy)及肿瘤局部加量照射(20 Gy)。
该方案患者的估计(Kaplan-Meier法)无事件生存率(EFS)为0.57±0.09(n = 28),无复发生存率(RFS)在5年和10年时为0.67±0.10。关于长期生存,诊断时明显的神经系统症状与原发肿瘤切除的联合似乎是主要的不良预后危险因素(Fisher精确检验p < 0.05)。诊断时的中枢神经系统播散也可被视为不良危险因素,因为5例原发播散患者中有3例死于该疾病。
以顺铂为基础的三联化疗,随后切除残留肿瘤并进行全脑全脊髓照射(CSI)及肿瘤局部加量照射,是治疗secCNSGCTs的一种成功且耐受性良好的方法。基于MRI和肿瘤标志物进行临床诊断的可能性以及现代神经外科技术的应用,使我们有机会推迟甚至避免大型手术。这为降低急性发病率和进一步减少晚期效应提供了额外机会。