首页> 外文期刊>Cancer chemotherapy and pharmacology. >Plasma and cerebrospinal fluid pharmacokinetics of topotecan in a phase I trial of topotecan, tamoxifen, and carboplatin, in the treatment of recurrent or refractory brain or spinal cord tumors.
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Plasma and cerebrospinal fluid pharmacokinetics of topotecan in a phase I trial of topotecan, tamoxifen, and carboplatin, in the treatment of recurrent or refractory brain or spinal cord tumors.

机译:拓扑替康,他莫昔芬和卡铂的I期临床试验中,拓扑替康的血浆和脑脊液药代动力学用于治疗复发或难治性脑或脊髓肿瘤。

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PURPOSE: This study was designed to ascertain the dose-limiting toxicities (DLT) and maximally tolerated doses of the combination of fixed-dose tamoxifen and carboplatin, with escalating doses of topotecan, and to determine the pharmacokinetics of topotecan in the plasma and cerebrospinal fluid. METHODS: Tamoxifen 100 mg po bid, topotecan 0.25, 0.5, 0.75, or 1.0 mg/m(2)/d IV, administered as a 72 h continuous infusion on days 1-3, followed by carboplatin AUC = 3, IV on day 3. Cycles were repeated every 4 weeks. RESULTS: Seventeen patients received 39 cycles of treatment: median 2, (range 1-5). The tumors included glioblastoma (6), anaplastic astrocytoma (2), metastatic non-small cell (3), small cell lung (2), and one each with medulloblastoma, ependymoma, and metastatic breast or colon carcinoma. The median Karnofsky performance status was 70% (range 60-90%) and age: 52 (range 24-75). Eleven patients were female and six male. Toxicities included thrombocytopenia (2), neutropenia without fever lasting 6 days (1), DVT (2), and emesis (1). Topotecan levels, total and lactone, were measured prior to the end of infusion in plasma and cerebrospinal fluid (CSF). At 1.0 mg/m(2)/d, the median CSF/plasma ratio was 19.4% (range 15.1-59.1%). The total plasma topotecan in two pts with DLTs was 4.63 and 5.87 ng/ml, in three without DLTs at the same dose level the mean total plasma topotecan was 3.4 ng/ml (range 3.02-3.83). Plasma lactone levels were 33% of the total; CSF penetration was 20% of the total plasma levels. 4/8 pts with high-grade gliomas had stable disease (median: 3 cycles (range 2-5)). Two had minor responses. One patient with metastatic non-small cell and one with small cell lung cancer had objective PRs. CONCLUSIONS: The recommended phase II doses are: tamoxifen 100 mg po bid, topotecan 0.75 mg/m(2)/d IV continuous infusion for 72 h, followed by carboplatin AUC = 3 IV on day 3. Measurable topotecan levels, both total and lactone, are observed in the CSF.
机译:目的:本研究旨在确定固定剂量的他莫昔芬和卡铂联合递增剂量的拓扑替康的剂量极限毒性(DLT)和最大耐受剂量,并确定拓扑替康在血浆和脑脊髓液中的药代动力学。方法:他莫昔芬口服100 mg,拓扑替康0.25、0.5、0.75或1.0 mg / m(2)/ d IV,在第1-3天连续输注72小时,随后在一天中进行卡铂AUC = 3,IV 3.每4周重复一次周期。结果:17名患者接受了39个治疗周期:中位数2(范围1-5)。肿瘤包括胶质母细胞瘤(6),间变性星形细胞瘤(2),转移性非小细胞瘤(3),小细胞肺癌(2),以及每一个伴有髓母细胞瘤,室管膜瘤和转移性乳腺癌或结肠癌。卡诺夫斯基的中位表现状态为70%(范围60-90%),年龄:52(范围24-75)。十一名患者为女性,六名男性。毒性包括血小板减少症(2),持续6天无发热的嗜中性白血球减少症(1),DVT(2)和呕吐(1)。在输注血浆和脑脊髓液(CSF)之前,先测量总和内酯的拓扑替康水平。在1.0 mg / m(2)/ d时,CSF /血浆中位数比为19.4%(范围15.1-59.1%)。在两个具有DLT的患者中,总血浆拓扑替康的浓度分别为4.63和5.87 ng / ml,在三个不具有相同剂量水平的无DLT的患者中,其总血浆拓扑替康的平均含量为3.4 ng / ml(范围为3.02-3.83)。血浆内酯水平为总量的33%;脑脊液渗透率为总血浆水平的20%。患有高级别神经胶质瘤的患者中有4/8名患者病情稳定(中位数:3个周期(范围2-5))。两人反应不佳。转移性非小细胞患者1例,小细胞肺癌1例具有客观PR。结论:推荐的II期推荐剂量为:他莫昔芬口服100 mg,托泊替康0.75 mg / m(2)/ d,连续静脉输注72 h,然后在第3天卡铂AUC = 3 IV。可测的总拓扑替康水平在脑脊液中观察到内酯。

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