Brem H, Gabikian P
Johns Hopkins University School of Medicine Department of Neurological Surgery, 725 N. Wolfe Street, Baltimore, MD 21205, USA.
J Control Release. 2001 Jul 6;74(1-3):63-7. doi: 10.1016/s0168-3659(01)00311-x.
We have developed a systematic approach for the discovery and evaluation of local treatment strategies for brain tumors using polymers. We demonstrated the feasibility of polymer-mediated drug delivery by using the standard chemotherapeutic agent 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) and showed that local treatment of gliomas by this method is effective in animal models of intracranial tumors. This led to clinical trials for glioma patients, and subsequent approval of Gliadel [(3.8% BCNU): p(CPP:SA)] by the FDA and other worldwide regulatory agencies. Twenty-two additional clinical trials are currently underway evaluating other issues related to the BCNU polymer, such as dosage, combination with systemic treatments, and combination with various forms of radiation and resistance modifiers. These trials are a result of laboratory investigations using brain tumor models; based on these models, other research groups have initiated clinical trials with novel combinations of different drugs and new polymers for both intracranial tumors (5-fluorouracil delivered via poly(D-L lactide-co-glycolide) polymer) and for tumors outside the brain (paclitaxel in PPE microspheres for ovarian cancer). Since only 1/3 of patients with glioblastoma multiforme (GBM) are sensitive to BCNU, the need to search for additional drugs continues. Although we are attacking major resistance mechanisms, there still will be tumors that do not respond to BCNU therapy but are sensitive to agents with different mechanisms of action, such as taxanes, camptothecin, platinum drugs, and antiangiogenic agents. Thus, it is necessary to explore multiple single agents and ultimately to combine the most effective agents for the clinical treatment of GBM. Furthermore, multimodal approaches combining radiotherapy with microsphere delivery of cytokines and antiangiogenic agents have demonstrated encouraging results.
我们已经开发出一种系统方法,用于发现和评估使用聚合物对脑肿瘤进行局部治疗的策略。我们通过使用标准化疗药物1,3-双(2-氯乙基)-1-亚硝基脲(BCNU)证明了聚合物介导的药物递送的可行性,并表明通过这种方法对胶质瘤进行局部治疗在颅内肿瘤动物模型中是有效的。这导致了针对胶质瘤患者的临床试验,随后Gliadel [(3.8% BCNU):p(CPP:SA)] 获得了美国食品药品监督管理局(FDA)和其他全球监管机构的批准。目前还有另外22项临床试验正在进行,评估与BCNU聚合物相关的其他问题,如剂量、与全身治疗的联合、与各种形式的放疗和耐药性调节剂的联合。这些试验是使用脑肿瘤模型进行实验室研究的结果;基于这些模型,其他研究小组已经启动了针对颅内肿瘤(通过聚(D-L丙交酯-共-乙交酯)聚合物递送5-氟尿嘧啶)和脑外肿瘤(用于卵巢癌的PPE微球中的紫杉醇)的不同药物和新型聚合物新组合的临床试验。由于只有1/3的多形性胶质母细胞瘤(GBM)患者对BCNU敏感,因此继续寻找其他药物的需求仍然存在。尽管我们正在攻克主要的耐药机制,但仍会有一些肿瘤对BCNU治疗无反应,但对具有不同作用机制的药物敏感,如紫杉烷类、喜树碱、铂类药物和抗血管生成药物。因此,有必要探索多种单一药物,并最终将最有效的药物联合起来用于GBM的临床治疗。此外,将放疗与细胞因子和抗血管生成药物的微球递送相结合的多模式方法已经取得了令人鼓舞的结果。