University Cancer and Diagnostic Centers, Houston, Texas, USA.
University Cancer and Diagnostic Centers, Houston, Texas, USA,
Oncology. 2020;98(4):202-215. doi: 10.1159/000505487. Epub 2020 Feb 20.
Malignant melanoma represents the deadliest form of skin cancer with a high tendency to metastasize during the early course of the disease. Radiation therapy has long played a key role in the management of both local and metastatic melanoma. Although local radiation therapy exerts antitumor effects by damaging the cellular DNA, it also induces an important out-of-field (distant) effect known as the "abscopal effect" in nonirradiated sites. Radiation therapy-induced abscopal effects are believed to be mediated by activation and stimulation of the immune system.
To provide a detailed overview of the current state of knowledge and clinical experience of radiation therapy-induced abscopal effects in patients with malignant melanoma.
Using electronic databases such as MEDLINE via PubMed and Google Scholar, a systematic literature review was performed to find published clinical evidence for radiation therapy-induced abscopal effects in patients with malignant melanoma. The clinical data on radiation therapy-induced abscopal effects were reviewed and the outcomes summarized.
Clinical evidence of patients with malignant melanoma was gathered using databases from MEDLINE and those findings were summarized. Although the precise mechanism of the abscopal effect of radiation therapy is still not completely understood, evidence suggests that tumor cell destruction by radiation releases tumor antigens that stimulate the immune system of the host to activate the body's immune effector cells systemically and produce distant non-target antitumor effects. This forms a basis for using the radiation therapy with immunotherapy to augment the abscopal response rates.
Current clinical evidence suggests that there is a large potential to enhance the abscopal effect when radiation therapy is combined with immunotherapeutic agents for the treatment of malignant melanoma. Ongoing and planned clinical trials may provide us with a more in-depth understanding of how this combination therapy can be optimally utilized clinically to achieve improved survival outcomes among patients with malignant melanoma.
恶性黑色素瘤是皮肤癌中最致命的一种,在疾病早期有很高的转移倾向。放射治疗在局部和转移性黑色素瘤的治疗中一直起着关键作用。虽然局部放射治疗通过破坏细胞 DNA 发挥抗肿瘤作用,但它也会在未照射部位产生一种重要的场外(远处)效应,称为“远隔效应”。远隔效应被认为是通过激活和刺激免疫系统来介导的。
详细概述放射治疗诱导的恶性黑色素瘤患者远隔效应的现有知识和临床经验。
通过 MEDLINE 中的 PubMed 和 Google Scholar 等电子数据库进行系统文献回顾,以寻找发表的关于恶性黑色素瘤患者放射治疗诱导的远隔效应的临床证据。回顾放射治疗诱导的远隔效应的临床数据并总结结果。
使用来自 MEDLINE 的数据库收集了恶性黑色素瘤患者的临床证据,并对这些发现进行了总结。虽然放射治疗远隔效应的确切机制仍不完全清楚,但有证据表明,放射破坏肿瘤细胞会释放肿瘤抗原,刺激宿主的免疫系统,从而激活全身的免疫效应细胞,并产生远处非靶抗肿瘤效应。这为放射治疗联合免疫疗法增强远隔反应率提供了依据。
目前的临床证据表明,当放射治疗与免疫治疗药物联合用于治疗恶性黑色素瘤时,具有很大的增强远隔效应的潜力。正在进行和计划中的临床试验可能会为我们提供更深入的了解,了解如何在临床上最佳地利用这种联合治疗方法,以提高恶性黑色素瘤患者的生存结局。