Vera-Aguilera Jesus, Bedikian Agop Y, Bassett Roland L, Hwu Wen-Jen, Kim Kevin B, Qin Yong, Cain Suzanne, Washington Edwina W, Davies Michael A, Patel Sunil M, Homsi Jade, Papadopoulos Nicholas E, Hwu Patrick, Patel Sapna P
Departments of *Melanoma Medical Oncology †Biostatistics ‡General Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Am J Clin Oncol. 2018 Nov;41(11):1132-1136. doi: 10.1097/COC.0000000000000436.
Hepatic arterial infusion (HAI) of cytotoxic chemotherapy is a strategy to deliver high dose of anticancer therapy to liver metastases that derive their blood supply from the hepatic artery. Metastatic melanoma (MM) has a high incidence of liver metastases, with uveal subtype in particular exhibiting a predilection for liver dissemination. Nanoparticle albumin-bound paclitaxel (nab-paclitaxel) has demonstrated efficacy in MM and first-pass hepatic metabolism. Therefore, we hypothesized that HAI of nab-paclitaxel would deliver an effective dose of drug to the end organ of interest, with minimal systemic exposure.
We performed a single-institution open-label phase I/II study of HAI of nab-paclitaxel in MM patients with liver metastasis. Patients received treatment every 21 days at 4 different dose levels. The primary objective of the phase I portion of the study was safety and determination of the maximum-tolerated dose. The primary objective of the phase II portion of the study was overall response rate per Response Evaluation Criteria In Solid Tumors (RECIST) 1.0.
A total of 30 patients were treated between 2009 and 2013, 16 of whom had uveal melanoma. The maximum-tolerated dose was 220 mg/m and 19 patients were treated at this dose. There was 1 patient (5%) with a partial response at this dose, and 8 patients (42%) with stable disease at this dose.
HAI nab-paclitaxel demonstrates rare objective responses in melanoma patients with liver metastases. This treatment should be studied in combination with checkpoint blockade or other novel treatments to enhance meaningful responses but should not be considered effective monotherapy.
肝动脉灌注(HAI)细胞毒性化疗是一种向源自肝动脉供血的肝转移瘤输送高剂量抗癌治疗的策略。转移性黑色素瘤(MM)肝转移发生率高,尤其是葡萄膜亚型特别容易发生肝转移。纳米白蛋白结合型紫杉醇(nab-紫杉醇)已在MM及首过肝代谢方面显示出疗效。因此,我们推测HAI应用nab-紫杉醇可将有效剂量的药物输送至感兴趣的终末器官,同时使全身暴露降至最低。
我们在有肝转移的MM患者中开展了一项单机构开放标签的nab-紫杉醇HAI I/II期研究。患者每21天接受一次治疗,共4个不同剂量水平。该研究I期部分的主要目的是安全性及确定最大耐受剂量。该研究II期部分的主要目的是根据实体瘤疗效评价标准(RECIST)1.0评估的总缓解率。
2009年至2013年间共治疗了30例患者,其中16例为葡萄膜黑色素瘤。最大耐受剂量为220mg/m²,19例患者接受了该剂量治疗。该剂量下有1例患者(5%)出现部分缓解,8例患者(42%)病情稳定。
HAI应用nab-紫杉醇在有肝转移的黑色素瘤患者中显示出罕见的客观缓解。该治疗应与检查点阻断或其他新疗法联合研究以增强有意义的缓解,但不应被视为有效的单一疗法。