Advances in immunotherapy for melanoma

被引:0
作者
Jason M. Redman
Geoffrey T. Gibney
Michael B. Atkins
机构
[1] Georgetown Lombardi Comprehensive Cancer Center 3970 Reservoir Road,Department of Medicine
[2] NW Research Building,undefined
[3] Room E501,undefined
[4] Georgetown University Medical Center,undefined
来源
BMC Medicine | / 14卷
关键词
Anti-PD-1; Immunotherapy; Ipilimumab; Melanoma; Nivolumab; Pembrolizumab;
D O I
暂无
中图分类号
学科分类号
摘要
In recent years, the introduction and Federal Drug Administration approval of immune checkpoint inhibitor antibodies has dramatically improved the clinical outcomes for patients with advanced melanoma. These antagonist monoclonal antibodies are capable of unleashing dormant or exhausted antitumor immunity, which has led to durable complete and partial responses in a large number of patients. Ipilimumab targets the cytotoxic T lymphocyte-associated protein 4 (CTLA-4) receptor. Nivolumab and pembrolizumab target programmed cell death protein 1 (PD-1) receptors and have proven to be superior to ipilimumab alone. The combination of ipilimumab and nivolumab has yielded higher response rates, greater tumor shrinkage, and longer progression-free survival than either monotherapy alone. As other promising immunotherapies for melanoma proceed through clinical trials, future goals include defining the role of immune checkpoint inhibitors as adjuvant therapy, identifying optimal combination strategies, and developing reliable predictive biomarkers to guide treatment selection for individual patients.
引用
收藏
相关论文
共 380 条
  • [1] Garbe C(2011)Systematic review of medical treatment in melanoma: current status and future prospects Oncologist 16 5-24
  • [2] Eigentler TK(2000)Randomized phase III study of temozolomide versus dacarbazine in the treatment of patients with advanced metastatic malignant melanoma J Clin Oncol 18 158-66
  • [3] Keilholz U(1985)Observations on the systemic administration of autologous lymphokine-activated killer cells and recombinant interleukin-2 to patients with metastatic cancer N Engl J Med 313 1485-92
  • [4] Hauschild A(1992)Image analysis of stage 1 melanoma (1.00-2.50 mm): lymphocytic infiltrates related to metastasis and survival J Cutan Pathol 19 390-397
  • [5] Kirkwood JM(1983)Factors associated with death from melanoma from 2 to 5 years following diagnosis in clinical stage I patients J Invest Dermatol 80 Suppl 53s-55s
  • [6] Middleton MR(1999)High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993 J Clin Oncol 17 2105-16
  • [7] Grob JJ(2006)Tumor progression despite massive influx of activated CD8(+) T cells in a patient with malignant melanoma ascites Cancer Immunol Immunother 55 1185-97
  • [8] Aaronson N(2013)Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells Sci Transl Med 5 200ra116-5
  • [9] Fierlbeck G(2003)B7-H1 blockade augments adoptive T-cell immunotherapy for squamous cell carcinoma Cancer Res 63 6501-34
  • [10] Tilgen W(2007)Programmed death-1 blockade enhances expansion and functional capacity of human melanoma antigen-specific CTLs Int Immunol 19 1223-46