作者: Amber L. Shada , Kerrington R. Molhoek , Craig L. Slingluff
DOI: 10.1097/PPO.0B013E3181EB3393
关键词: Immune system 、 Immunotherapy 、 Drug 、 Immunology 、 Melanoma 、 Alpha interferon 、 Cancer research 、 Signal Transduction Inhibition 、 Signal transduction 、 Targeted therapy 、 Medicine 、 Oncology
摘要: Food and Drug Administration-approved treatment for metastatic melanoma, including interferon alpha interleukin-2, offer a modest benefit. Immunotherapy, although has not enjoyed high overall response rates, is capable of providing durable responses in subset patients. In recent years, new molecular-targeted therapies have become available promise clinical benefit, low durability response. It yet clear how best to integrate these 2 novel modalities that target the immune melanoma (immune therapy) or molecular signaling pathways cells (targeted therapy). Many signal transduction are important both tumor cell T-cell proliferation survival, which generate risk combining targeted therapy immunotherapy. This review focuses on role immunotherapy discusses combine rationally increased duration