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