期刊
NATURE REVIEWS CLINICAL ONCOLOGY
卷 17, 期 11, 页码 707-715出版社
NATURE RESEARCH
DOI: 10.1038/s41571-020-0399-6
关键词
-
类别
资金
- Abbvie
- Amgen
- AstraZeneca
- Biogen
- Blueprint Medicines
- BMS
- Celgene
- Eli Lilly
- GSK
- Ignyta
- Ipsen
- Merck
- MSD
- Nektar
- Onxeo
- Pfizer
- Pharma Mar
- Sanofi
- Spectrum Pharmaceuticals
- Takeda
- Tiziana Pharm
The availability and subsequent successes of immune-checkpoint inhibitors (ICIs) in patients with metastatic melanoma, and to a lesser extent in those with several other forms of cancer, have made long-term treatment-free remissions a realistic possibility for a subset of patients. In this Perspective, the authors describe available data on long-term remission from patients with melanoma and other solid tumours and provide early recommendations regarding the circumstances in which ICIs can be safely discontinued. The optimal duration of therapy in patients receiving immune-checkpoint inhibitors (ICIs) is a new but crucial question that has arisen owing to the observation of durable remissions in >85% of patients with metastatic melanoma who stop receiving an anti-PD-1 antibody after a complete response (CR). Long-term treatment-free remissions have also been seen, albeit much less frequently, in patients receiving ICIs for other forms of cancer who have a CR. Despite these promising observations, the optimal duration of treatment with ICIs remains unknown and requires further investigation in randomized controlled trials. In the absence of prospective data, some general criteria to guide the safe cessation of ICIs can be proposed, at least for patients with melanoma, in whom ICI cessation after a confirmed CR and at least 6 months of treatment is generally deemed safe. In this Perspective, we describe the available data on ICI interruption in patients with melanoma and in those with various other cancers. We also address the patient management implications of stopping ICI therapy.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据