Baldwin Paige, Likhotvorik Rostislav, Baig Nabeela, Cropper Jodie, Carlson Ruth, Kurmasheva Raushan, Sridhar Srinivas
Department of Bioengineering, Northeastern University, Boston, MA, United States.
Greehey Children's Cancer Research Institute, San Antonio, TX, United States.
Front Oncol. 2019 Dec 17;9:1416. doi: 10.3389/fonc.2019.01416. eCollection 2019.
The Pediatric Preclinical Testing Program previously identified the PARP inhibitor talazoparib (TLZ) as a means to potentiate temozolomide (TMZ) activity for the treatment of Ewing sarcoma. However, the combination of TLZ and TMZ has been toxic in both preclinical and clinical testing, necessitating TMZ dose reduction to ~15% of the single agent maximum tolerated dose. We have synthesized a nanoparticle formulation of talazoparib (NanoTLZ) to be administered intravenously in an effort to modulate the toxicity profile of this combination treatment. Results in Ewing sarcoma xenograft models are presented to demonstrate the utility of this delivery method both alone and in combination with TMZ. NanoTLZ reduced gross toxicity and had a higher maximum tolerated dose than oral TLZ. The dose of TMZ did not have to be reduced when combined with NanoTLZ as was required when combined with oral TLZ. This indicated the NanoTLZ delivery system may be advantageous in decreasing the systemic toxicity associated with the combination of oral TLZ and TMZ.
儿科临床前测试项目先前已确定聚(ADP - 核糖)聚合酶(PARP)抑制剂他拉唑帕尼(TLZ)可增强替莫唑胺(TMZ)治疗尤因肉瘤的活性。然而,在临床前和临床试验中,TLZ与TMZ的联合使用均具有毒性,这就需要将TMZ剂量降至单药最大耐受剂量的约15%。我们合成了他拉唑帕尼纳米颗粒制剂(NanoTLZ)用于静脉给药,以调节这种联合治疗的毒性特征。本文展示了尤因肉瘤异种移植模型的结果,以证明这种给药方法单独使用以及与TMZ联合使用的效用。NanoTLZ降低了总体毒性,并且比口服TLZ具有更高的最大耐受剂量。与口服TLZ联合使用时不同,与NanoTLZ联合使用时无需降低TMZ的剂量。这表明NanoTLZ给药系统在降低与口服TLZ和TMZ联合使用相关的全身毒性方面可能具有优势。