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恩扎妥林(LY317615)联合贝伐单抗治疗复发性恶性胶质瘤成人患者的II期试验。

A phase II trial of enzastaurin (LY317615) in combination with bevacizumab in adults with recurrent malignant gliomas.

作者信息

Odia Yazmin, Iwamoto Fabio M, Moustakas Argirios, Fraum Tyler J, Salgado Carlos A, Li Aiguo, Kreisl Teri N, Sul Joohee, Butman John A, Fine Howard A

机构信息

Neuro-Oncology Division, Neurological Institute of New York, Columbia University College of Physicians and Surgeons, 710 West 168th Street, 9th Floor, NI 9-017, New York, NY, 10032, USA.

University of Vermont Medical Center, 89 South Williams Street, Burlington, VT, 05401, USA.

出版信息

J Neurooncol. 2016 Mar;127(1):127-35. doi: 10.1007/s11060-015-2020-x. Epub 2015 Dec 7.

Abstract

We evaluated the efficacy of combination enzastaurin (LY317615) and bevacizumab for recurrent malignant gliomas and explored serologic correlates. We enrolled 81 patients with glioblastomas (GBM, n = 40) and anaplastic gliomas (AG, n = 41). Patients received enzastaurin as a loading dose of 1125 mg, followed by 500 or 875 mg daily for patients on non-enzyme-inducing or enzyme-inducing antiepileptics, respectively. Patients received bevacizumab 10 mg/kg intravenously biweekly. Clinical evaluations were repeated every 4 weeks. Magnetic resonance imaging was obtained at baseline and every 8 weeks from treatment onset. Phosphorylated glycogen synthase kinase (GSK)-3 levels from peripheral blood mononuclear cells (PBMCs) were checked with each MRI. Median overall survival was 7.5 and 12.4 months for glioblastomas and anaplastic glioma cohorts, with median progression-free survivals of 2.0 and 4.4 months, respectively. Of GBM patients, 3/40 (7.5 %) were not evaluable, while 8/37 (22 %) had partial or complete response and 20/37 (54 %) had stable disease for 2+ months. Of the 39 evaluable AG patients, 18 (46 %) had an objective response, and 16 (41 %) had stable disease for 2+ months. The most common grade 3+ toxicities were lymphopenia (15 %), hypophosphatemia (8.8 %) and thrombotic events (7.5 %). Two (2.5 %) GBM patients died suddenly; another death (1.3 %) occurred from intractable seizures. Phosphorylated GSK-3 levels from PBMCs did not correlate with treatment response. A minimally important improvement in health-related quality of life was self-reported in 7-9/24 (29.2-37.5 %). Early response based on Levin criteria was significantly associated with significantly longer progression free survival for glioblastomas. Enzastaurin (LY317615) in combination with bevacizumab for recurrent malignant gliomas is well-tolerated, with response and progression-free survival similar to bevacizumab monotherapy.

摘要

我们评估了恩杂他滨(LY317615)与贝伐单抗联合用药对复发性恶性胶质瘤的疗效,并探索了血清学相关因素。我们纳入了81例胶质母细胞瘤(GBM,n = 40)和间变性胶质瘤(AG,n = 41)患者。患者接受1125 mg的恩杂他滨负荷剂量,随后对于未使用酶诱导型或酶诱导型抗癫痫药物的患者,分别每日给予500或875 mg。患者每两周静脉注射10 mg/kg贝伐单抗。每4周重复进行临床评估。在基线时以及从治疗开始每8周进行一次磁共振成像检查。每次磁共振成像检查时均检测外周血单核细胞(PBMC)中的磷酸化糖原合酶激酶(GSK)-3水平。胶质母细胞瘤和间变性胶质瘤队列的中位总生存期分别为7.5个月和12.4个月,中位无进展生存期分别为2.0个月和4.4个月。在GBM患者中,3/40(7.5%)不可评估,而8/37(22%)有部分或完全缓解,20/37(54%)疾病稳定2个月以上。在39例可评估的AG患者中,18例(46%)有客观缓解,16例(41%)疾病稳定2个月以上。最常见的3级及以上毒性反应为淋巴细胞减少(15%)、低磷血症(8.8%)和血栓形成事件(7.5%)。2例(2.5%)GBM患者突然死亡;另1例死亡(1.3%)因难治性癫痫发作。PBMC中的磷酸化GSK-3水平与治疗反应无关。24例患者中有7 - 9例(29.2 - 37.5%)自我报告健康相关生活质量有最小重要改善。基于Levin标准的早期反应与胶质母细胞瘤显著更长的无进展生存期显著相关。恩杂他滨(LY317615)与贝伐单抗联合用于复发性恶性胶质瘤耐受性良好,反应和无进展生存期与贝伐单抗单药治疗相似。

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