Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
J Dermatol. 2018 Sep;45(9):1105-1108. doi: 10.1111/1346-8138.14508. Epub 2018 Jun 20.
Although therapies for advanced melanoma have been greatly improved by the development of immune checkpoint inhibitors and BRAF/mitogen-activated protein kinase kinase inhibitors, there are still many concerns about the administration of these novel drugs. Therefore, to combine these therapies sequentially at appropriate time points of the disease is important. In this report, we report two cases in which dabrafenib and trametinib therapy for advanced melanoma failed but were successfully controlled by nivolumab monotherapy, and investigated the sera sCD163, CCL22 and CXCL10 as biomarkers for tumor progression. Interestingly, the sera levels of sCD163, CXCL10 and CCL22, both of which are produced by activated tumor-associated macrophages, were increased in parallel with the tumor progression in each case. Because this report presents only two cases, further data will need to be accumulated to provide more fundamental insights into the usefulness of these biomarkers for predicting disease progression in melanoma.
虽然免疫检查点抑制剂和 BRAF/丝裂原活化蛋白激酶激酶抑制剂的发展极大地改善了晚期黑色素瘤的治疗方法,但对于这些新型药物的应用仍存在许多顾虑。因此,在疾病的适当时间点将这些治疗方法序贯联合应用非常重要。在本报告中,我们报告了两例晚期黑色素瘤患者接受 dabrafenib 和 trametinib 治疗失败,但接受 nivolumab 单药治疗后成功得到控制的病例,并研究了血清 sCD163、CCL22 和 CXCL10 作为肿瘤进展的生物标志物。有趣的是,与每个病例的肿瘤进展平行的是,由激活的肿瘤相关巨噬细胞产生的血清 sCD163、CXCL10 和 CCL22 水平均升高。由于本报告仅涉及两例病例,需要进一步积累数据,以更深入地了解这些生物标志物在预测黑色素瘤疾病进展方面的有用性。