Mayo Clinic, Rochester, Minnesota, USA
Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.
Oncologist. 2017 Sep;22(9):1026-e93. doi: 10.1634/theoncologist.2017-0060. Epub 2017 Jul 5.
Percutaneous thermal ablation combined with in situ granulocyte-macrophage colony-stimulating factor cytokine therapy was technically feasible and well tolerated.No significant clinical or immunologic responses were seen.
Melanoma tumor-derived heat-shock proteins (HSPs) and HSP-peptide complexes can elicit protective antitumor responses. The granulocyte-macrophage colony-stimulating factor (GM-CSF) chemokine can also promote uptake and processing by professional antigen presenting cells (APCs). On this basis, we designed a pilot study of percutaneous thermal ablation as a means to induce heat-shock protein vaccination plus GM-CSF to determine safety and preliminary antitumor activity of this combination.
This study was designed to assess overall safety of percutaneous ablation combined with GM-CSF for unresectable, metastatic melanoma including uveal and mucosal types. All patients received heat-shock therapy (42°C for 30 minutes), then received one of three treatments: (a) intralesional GM-CSF (500 mcg standard dose); (b) radiofrequency ablation (RFA) + GM-CSF; or (c) cryoablation plus GM-CSF. The primary endpoint of the study was the induction of endogenous HSP70 and melanoma-specific cytotoxic T lymphocytes (CTL).
Nine patients (three per study arm) were enrolled. No dose-limiting toxicity was observed as specified per protocol. All patients developed progressive disease and went on to receive alternative therapy. Median overall survival (OS) was 8.2 months (95% confidence interval [CI] 2-17.2). The study was not powered to detect a difference in clinical outcome among treatment groups.
Percutaneous thermal ablation plus GM-CSF was well tolerated, technically feasible, and demonstrated an acceptable adverse event profile comparable to conventional RFA and cryoablation. While HSP70 was induced following therapy, the degree of HSP70 elevation was not associated with clinical outcome or induced CTL responses. While percutaneous thermal ablation plus GM-CSF combinations including checkpoint inhibitors could be considered in future studies, the use of GM-CSF remains experimental and for use in the context of clinical trials.
经皮热消融联合原位粒细胞-巨噬细胞集落刺激因子细胞因子治疗在技术上是可行的,且患者耐受性良好。未观察到明显的临床或免疫反应。
黑色素瘤肿瘤来源的热休克蛋白(HSPs)和 HSP-肽复合物可以引发保护性抗肿瘤反应。粒细胞-巨噬细胞集落刺激因子(GM-CSF)趋化因子也可以促进专业抗原呈递细胞(APCs)的摄取和处理。在此基础上,我们设计了一项经皮热消融作为诱导热休克蛋白疫苗接种加 GM-CSF 的初步研究,以确定这种联合治疗的安全性和初步抗肿瘤活性。
本研究旨在评估不可切除转移性黑色素瘤(包括葡萄膜和黏膜类型)患者经皮消融联合 GM-CSF 的总体安全性。所有患者均接受热休克治疗(42°C 30 分钟),然后接受以下三种治疗之一:(a)瘤内 GM-CSF(500mcg 标准剂量);(b)射频消融(RFA)+GM-CSF;或(c)冷冻消融加 GM-CSF。该研究的主要终点是诱导内源性 HSP70 和黑色素瘤特异性细胞毒性 T 淋巴细胞(CTL)。
共纳入 9 名患者(每个研究组 3 名)。按照方案规定,未观察到剂量限制性毒性。所有患者均出现进行性疾病,并接受了替代治疗。中位总生存期(OS)为 8.2 个月(95%置信区间 [CI] 2-17.2)。该研究没有足够的效力来检测治疗组之间临床结果的差异。
经皮热消融联合 GM-CSF 具有良好的耐受性、技术可行性,且表现出可接受的不良事件谱,与常规 RFA 和冷冻消融相当。尽管治疗后诱导了 HSP70,但 HSP70 的升高程度与临床结果或诱导的 CTL 反应无关。虽然包括检查点抑制剂在内的经皮热消融联合 GM-CSF 组合可在未来的研究中考虑,但 GM-CSF 的使用仍然是实验性的,仅在临床试验的背景下使用。