Trojaniello Claudia, Luke Jason J, Ascierto Paolo A
Unit of Melanoma, Cancer Immunotherapy and Development Therapeutics, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.
Cancer Immunotherapeutics Center, University of Pittsburgh Medical Center and Hillman Cancer Center, Pittsburgh, PA, United States.
Front Oncol. 2021 Jun 10;11:670726. doi: 10.3389/fonc.2021.670726. eCollection 2021.
Melanoma is the most fatal skin cancer. In the early stages, it can be safely treated with surgery alone. However, since 2011, there has been an important revolution in the treatment of melanoma with new effective treatments. Targeted therapy and immunotherapy with checkpoint inhibitors have changed the history of this disease. To date, more than half of advanced melanoma patients are alive at 5 years; despite this breakthrough, approximately half of the patients still do not respond to treatment. For these reasons, new therapeutic strategies are required to expand the number of patients who can benefit from immunotherapy or combination with targeted therapy. Current research aims at preventing primary and acquired resistance, which are both responsible for treatment failure in about 50% of patients. This could increase the effectiveness of available drugs and allow for the evaluation of new combinations and new targets. The main pathways and molecules under study are the IDO inhibitor, TLR9 agonist, STING, LAG-3, TIM-3, HDAC inhibitors, pegylated IL-2 (NKTR-214), GITR, and adenosine pathway inhibitors, among others (there are currently about 3000 trials that are evaluating immunotherapeutic combinations in different tumors). Other promising strategies are cancer vaccines and oncolytic viruses. Another approach is to isolate and remove immune cells (DCs, T cells, and NK cells) from the patient's blood or tumor infiltrates, add specific gene fragments, expand them in culture with growth factors, and re-inoculate into the same patient. TILs, TCR gene transfer, and CAR-T therapy follow this approach. In this article, we give an overview over the current status of melanoma therapies, the clinical rationale for choosing treatments, and the new immunotherapy approaches.
黑色素瘤是最致命的皮肤癌。在早期阶段,仅通过手术就能安全地进行治疗。然而,自2011年以来,随着新的有效治疗方法的出现,黑色素瘤的治疗发生了重大变革。靶向治疗和免疫检查点抑制剂免疫疗法改变了这种疾病的治疗史。迄今为止,超过一半的晚期黑色素瘤患者能存活5年;尽管有这一突破,但仍有大约一半的患者对治疗没有反应。出于这些原因,需要新的治疗策略来扩大能够从免疫疗法或与靶向治疗联合中获益的患者数量。当前的研究旨在预防原发性和获得性耐药,这两者约占50%患者治疗失败的原因。这可能会提高现有药物的疗效,并有助于评估新的联合用药和新的靶点。正在研究的主要途径和分子包括吲哚胺2,3-双加氧酶(IDO)抑制剂、Toll样受体9(TLR9)激动剂、干扰素基因刺激蛋白(STING)、淋巴细胞激活基因3(LAG-3)、T细胞免疫球蛋白和粘蛋白域蛋白3(TIM-3)、组蛋白去乙酰化酶(HDAC)抑制剂、聚乙二醇化白细胞介素-2(NKTR-214)、糖皮质激素诱导的肿瘤坏死因子受体(GITR)以及腺苷途径抑制剂等(目前约有3000项试验正在评估不同肿瘤中的免疫治疗联合用药)。其他有前景的策略包括癌症疫苗和溶瘤病毒。另一种方法是从患者的血液或肿瘤浸润物中分离并去除免疫细胞(树突状细胞、T细胞和自然杀伤细胞),添加特定的基因片段,用生长因子在培养中扩增它们,然后重新接种到同一患者体内。肿瘤浸润淋巴细胞(TILs)、T细胞受体(TCR)基因转移和嵌合抗原受体T细胞(CAR-T)疗法都遵循这种方法。在本文中,我们概述了黑色素瘤治疗的现状、选择治疗方法的临床依据以及新的免疫治疗方法。