Jaeckle Kurt A, Batchelor Tracy, O'Day Steven J, Phuphanich Surasak, New Pamela, Lesser Glenn, Cohn Allen, Gilbert Mark, Aiken Robert, Heros Deborah, Rogers Lisa, Wong Eric, Fulton Dorcas, Gutheil John C, Baidas Said, Kennedy Julia M, Mason Warren, Moots Paul, Russell Christy, Swinnen Lode J, Howell Stephen B
Mayo Clinic, Jacksonville, FL, USA.
J Neurooncol. 2002 May;57(3):231-9. doi: 10.1023/a:1015752331041.
Drugs currently available for intrathecal administration are cleared rapidly from the CSF. DepoCyt is a slow-release formulation of cytarabine that maintains cytotoxic concentrations of free cytarabine in the CSF for >14 days following a single injection. DepoCyt was administered to 110 patients with a diagnosis of neoplastic meningitis based on either a positive CSF cytology (76) or neurologic and CT or MRI scan findings sufficient to document neoplastic meningitis (34). Patients were treated with DepoCyt 50mg every 2 weeks for 1 month of induction therapy by either lumbar puncture (LP) or intraventricular (IVT) injection. Patients without neurologic progression were candidates to receive an additional 3 months of consolidation therapy. All patients received dexamethasone 4 mg BID on days 1-5 of each cycle. Median time to neurologic progression was 55 days; median overall survival was 95 days. Among the 76 patients with a positive CSF cytology at baseline, 70 were evaluable for response, and of this group 19 (27%) attained the criteria for response (cytologic response in the absence of neurologic progression). The most important adverse events were headache and arachnoiditis. When drug-related, these were largely low grade, transient, and reversible. Drug-related grade 3 headache occurred on 4% of cycles; grade 3 or 4 arachnoiditis occurred on 6% of cycles. No cumulative toxicity was observed. DepoCyt injected once every 2 weeks produced a response-rate comparable to that previously reported for methotrexate given twice a week. The once in every 2-week-dosing interval offers an advantage over conventional schedules (2-3 doses/week) used for other agents available for intrathecal injection.
目前可用于鞘内给药的药物会迅速从脑脊液中清除。DepoCyt是阿糖胞苷的缓释制剂,单次注射后可在脑脊液中维持游离阿糖胞苷的细胞毒性浓度超过14天。110例诊断为肿瘤性脑膜炎的患者接受了DepoCyt治疗,这些患者基于脑脊液细胞学检查阳性(76例)或足以确诊肿瘤性脑膜炎的神经学及CT或MRI扫描结果(34例)。患者通过腰椎穿刺(LP)或脑室内(IVT)注射,每2周接受50mg DepoCyt治疗,进行为期1个月的诱导治疗。无神经学进展的患者有资格接受额外3个月的巩固治疗。所有患者在每个周期的第1 - 5天接受地塞米松4mg,每日两次。至神经学进展的中位时间为55天;中位总生存期为95天。在基线时脑脊液细胞学检查阳性的76例患者中,70例可评估反应,其中19例(27%)达到反应标准(在无神经学进展的情况下出现细胞学反应)。最重要的不良事件是头痛和蛛网膜炎。与药物相关时,这些大多为低级别、短暂且可逆的。与药物相关的3级头痛在4%的周期中出现;3级或4级蛛网膜炎在6%的周期中出现。未观察到累积毒性。每2周注射一次DepoCyt产生的反应率与先前报道的每周两次给予甲氨蝶呤的反应率相当。每2周一次的给药间隔比用于其他鞘内注射可用药物的传统给药方案(每周2 - 3剂)具有优势。