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恩扎妥滨联合替莫唑胺与放疗治疗多形性胶质母细胞瘤:一项 I 期研究。

Enzastaurin plus temozolomide with radiation therapy in glioblastoma multiforme: a phase I study.

机构信息

Department of Neurological Surgery, University of California San Francisco, 400 Parnassus Avenue, A808, San Francisco, CA 94143-0350, USA.

出版信息

Neuro Oncol. 2010 Jun;12(6):608-13. doi: 10.1093/neuonc/nop070. Epub 2010 Feb 15.

Abstract

We conducted a phase I study to determine the safety and recommended phase II dose of enzastaurin (oral inhibitor of the protein kinase C-beta [PKCbeta] and the PI3K/AKT pathways) when given in combination with radiation therapy (RT) plus temozolomide to patients with newly diagnosed glioblastoma multiforme or gliosarcoma. Patients with Karnofsky performance status > or =60 and no enzyme-inducing anti-epileptic drugs received RT (60 Gy) over 6 weeks, concurrently with temozolomide (75 mg/m(2) daily) followed by adjuvant temozolomide (200 mg/m(2)) for 5 days/28-d cycle. Enzastaurin was given once daily during RT and adjuvantly with temozolomide; the starting dose of 250 mg/d was escalated to 500 mg/d if < or =1/6 patients had dose-limiting toxicity (DLT) during RT and the first adjuvant cycle. Patients continued treatment for 12 adjuvant cycles unless disease progression or unacceptable toxicity occurred. Twelve patients enrolled. There was no DLT in the first 6 patients treated with 250 mg enzastaurin. At 500 mg, 2 of 6 patients experienced a DLT (1 Grade 4 and 1 Grade 3 thrombocytopenia). The patient with Grade 3 DLT recovered to Grade <1 within 28 days and adjuvant temozolomide and enzastaurin was reinitiated with dose reductions. The other patient recovered to Grade <1 toxicity after 28 days and did not restart treatment. Enzastaurin 250 mg/d given concomitantly with RT and temozolomide and adjuvantly with temozolomide was well tolerated and is the recommended phase II dose. The proceeding phase II trial has finished accrual and results will be reported in 2009.

摘要

我们进行了一项 I 期研究,以确定在联合放疗(RT)和替莫唑胺治疗新诊断的胶质母细胞瘤或多形性成胶质细胞瘤或肉瘤患者时,恩扎司琼(蛋白激酶 C-β [PKCβ]和 PI3K/AKT 通路的口服抑制剂)的安全性和推荐的 II 期剂量。卡诺夫斯基表现状态 > 或 =60,且没有诱导酶的抗癫痫药物的患者接受 RT(60 Gy)6 周,同时给予替莫唑胺(75 mg/m2)每日一次,随后接受辅助性替莫唑胺(200 mg/m2)5 天/28 天周期。恩扎司琼在 RT 期间每日一次给药,并在辅助性替莫唑胺治疗时给药;如果在 RT 和第一个辅助周期中 < 或 =1/6 名患者出现剂量限制毒性(DLT),则将起始剂量 250 mg/d 升高至 500 mg/d。患者继续接受治疗 12 个辅助周期,除非疾病进展或出现不可接受的毒性。12 名患者入组。前 6 名接受 250 mg 恩扎司琼治疗的患者中没有 DLT。在 500 mg 时,6 名患者中有 2 名发生 DLT(1 级 4 级和 1 级 3 级血小板减少症)。3 级 DLT 患者在 28 天内恢复至 <1 级,并重新开始辅助性替莫唑胺和恩扎司琼治疗,剂量减少。另一名患者在 28 天后恢复至 <1 级毒性,未重新开始治疗。恩扎司琼 250 mg/d 与 RT 和替莫唑胺同时给药,并与替莫唑胺辅助给药,耐受性良好,是推荐的 II 期剂量。随后的 II 期试验已完成入组,结果将于 2009 年公布。

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