Paclitaxel and Carboplatin in Combination with Low-intensity Pulsed Ultrasound for Glioblastoma

被引:5
作者
Habashy, Karl J. [1 ,2 ]
Dmello, Crismita [1 ,2 ]
Chen, Li [1 ,2 ]
Arrieta, Victor A. [1 ,2 ]
Kim, Kwang-Soo [1 ,2 ]
Gould, Andrew [1 ,2 ]
Youngblood, Mark W. [1 ,2 ]
Bouchoux, Guillaume [3 ]
Burdett, Kirsten B. [4 ]
Zhang, Hui [2 ,4 ]
Canney, Michael [3 ]
Stupp, Roger [1 ,2 ,5 ,6 ]
Sonabend, Adam M. [1 ,2 ,7 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Neurol Surg, Chicago, IL USA
[2] Northwestern Univ, Northwestern Med Lou & Jean Malnati Brain Tumor In, Feinberg Sch Med, Chicago, IL USA
[3] Carthera, Lyon, France
[4] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL USA
[5] Northwestern Univ Feinberg, Sch Med, Dept Neurol, Chicago, IL USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Hematol & Oncol, Chicago, IL USA
[7] Northwestern Univ, 676 N St Clair, Chicago, IL 60611 USA
关键词
BLOOD-BRAIN-BARRIER; ALBUMIN-BOUND PACLITAXEL; CANCER CELL-LINES; RECURRENT GLIOBLASTOMA; FOCUSED ULTRASOUND; OVARIAN-CANCER; BREAST-CANCER; CHEMOTHERAPY; DELIVERY; LUNG;
D O I
10.1158/1078-0432.CCR-23-2367
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We recently reported on clinical trials for patients with recurrent glioblastoma where low-intensity pulsed ultrasound and microbubbles (LIPU/MB) improved paclitaxel or carboplatin delivery into the brain. Here, we report variable local tumor control with paclitaxel at the maximal/target dose in our phase I trial (NCT04528680). To address this, we investigated the combination of paclitaxel with carboplatin in preclinical glioma models.Experimental Design: We performed MRI-based analysis to evaluate disease control in patients from our trial. We studied the cytotoxicity of paclitaxel and carboplatin against 11 human glioma lines as monotherapy and in combination at concentrations derived from human intraoperative studies. Synergy was assessed with the Loewe model and the survival benefit evaluated in two xenografts. We examined the effects on cell cycle progression, DNA damage, and apoptosis.Results: Patients treated with paclitaxel and LIPU/MB exhibited variable local tumor control, which correlated with overall survival. We observed limited cross-resistance to paclitaxel and carboplatin in glioma lines, with almost a third of them being exclusively susceptible to one drug. This combination led to susceptibility of 81% of lines and synergy in 55% of them. The combination proved more efficacious in two intracranial xenografts when administered with LIPU/MB, leading to complementary effects on cell cycle arrest.Conclusions: Combining paclitaxel and carboplatin in gliomas may be more efficacious than monotherapy, as in other cancers, due to synergy and independent susceptibility to each drug. These results form the basis for an ongoing phase II trial (NCT04528680) where we investigate this combination with LIPU/MB.
引用
收藏
页码:1619 / 1629
页数:11
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