Adjuvant immunotherapy for melanoma patients: progress and opportunities

被引:2
|
作者
Sussman, T. A. [1 ,2 ,3 ]
Ott, P. A. [1 ,2 ,3 ,4 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA USA
[3] Harvard Med Sch, Boston, MA USA
[4] Dana Farber Canc Inst, DA-02126, 450 Brookline Ave, Boston, MA 02115 USA
关键词
melanoma; PD-1; inhibition; T cells; adjuvant; neoadjuvant; immunotherapy; STAGE-III MELANOMA; DOUBLE-BLIND; IPILIMUMAB; NIVOLUMAB; THERAPY; SURVIVAL; PLACEBO; CANCER; TRIAL;
D O I
10.1016/j.esmoop.2024.102962
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The majority of patients who are diagnosed with cutaneous melanoma are candidates for surgical resection and thus curable from their disease. However, the risk for a recurrence is high for many patients, including those with lymph node-negative melanoma, thus necessitating additional therapies beyond surgery. With the advent of antiprogrammed cell death protein 1 (PD-1)-based immunotherapies, which are vastly more effective compared to previous standard-of-care treatments in the advanced setting, the landscape of adjuvant therapy has fundamentally changed in recent years. Anti-PD-1-based immune checkpoint inhibition therapy is now the standard of care for many patients with stage IIB or higher melanoma. Neoadjuvant approaches have demonstrated superior outcomes compared to adjuvant-alone therapy. However, a number of questions remain including treatment combinations such as combined anti-PD-1 + lymphocyte activation gene-3, optimal sequencing of therapies, and the use of predictive markers to further improve outcomes for patients with high-risk melanoma.
引用
收藏
页数:8
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