乳腺癌
微波消融
阶段(地层学)
机会之窗
医学
窗口(计算)
肿瘤科
烧蚀
癌症
外科
内科学
生物
计算机科学
古生物学
实时计算
操作系统
作者
Hong Pan,Muxin Yu,Xinyu Tang,Xiao‐Ming Mao,Ming Liu,Kai Zhang,Chao-Nan Qian,Wang Ji,Hui Xie,Wen Qiu,Qiang Ding,Shui Wang,Wenbin Zhou
出处
期刊:Med
[Elsevier]
日期:2024-04-01
卷期号:5 (4): 291-310.e5
被引量:4
标识
DOI:10.1016/j.medj.2024.01.015
摘要
BackgroundImmune checkpoint blockade has shown low response rates for advanced breast cancer, and combination strategies are needed. Microwave ablation (MWA) may be a trigger of antitumor immunity. This window-of-opportunity trial (ClinicalTrials.gov: NCT04805736) was conducted to determine the safety and feasibility of preoperative camrelizumab (an anti-PD-1 antibody) combined with MWA in the treatment of early-stage breast cancer.MethodsSixty participants were randomized to preoperatively receive single-dose camrelizumab alone (n = 20), MWA alone (n = 20), or camrelizumab+MWA (n = 20). A random number table was used to allocate interventions. The primary outcome was the safety and feasibility of MWA combined with camrelizumab.FindingsCamrelizumab and MWA were well tolerated alone and in combination without delays in prescheduled surgery. No treatment-related grade III/IV adverse events were observed. Different from in the single-dose camrelizumab or MWA group, participants showed stable counts of blood cells after combination therapy. After combination therapy, peripheral CD8+ T cells showed enhanced cytotoxic and effect-memory functions. Clonal expansional CD8+ T cells showed higher cytotoxic activity and effector memory- and tumor-specific signatures than emergent clones after combination therapy. Enhanced interactions between clonal expansional CD8+ T cells and monocytes were observed, suggesting that monocytes contributed to the enhanced functions of clonal expansional CD8+ T cells. Major histocompatibility complex (MHC) class I-related pathways and interferon signaling pathways were activated in monocytes by combination therapy.ConclusionsCamrelizumab combined with MWA was feasible for early-stage breast cancer. Peripheral CD8+ T cells were activated after combination therapy, dependent on monocytes with activated MHC class I pathways.FundingThis study was supported by the Natural Science Foundation of Jiangsu Province (BK20230017).
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