免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Poorer survival outcomes in patients with multiple versus single primary melanoma.
Poorer survival outcomes in patients with multiple versus single primary melanoma.
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与 SPM 患者相比,MPM 患者的 RFS 和 OS 更差。
既往关于多原发黑色素瘤(MPM)和单原发黑色素瘤(SPM)患者总生存期(OS)的报告结果不一致,因此作者利用其UPCI-96-99数据库,评估所在中心这两组患者的OS是否存在差异。次要目标是评估无复发生存期(RFS)差异。部分患者还进行了外周血单个核细胞(PBMC)转录组分析,以评估与疾病相关的候选基因。
本回顾性病例对照研究按1:1比例纳入MPM患者及按年龄、性别和分期匹配的SPM对照。采用Cox回归模型评估MPM对死亡和复发的影响。采用NanoString泛癌免疫谱分析评估患者外周血免疫状态。
共评估320例患者,平均年龄47岁,男性占43.8%。MPM患者RFS和OS均较差(P分别为0.023和0.0019)。在校正年龄、性别和分期后,MPM与死亡风险增加相关(风险比[HR]=4.52,P=0.0006),也与疾病复发风险增加相关(HR=2.17,P=0.004)。MPM患者首次黑色素瘤与SPM患者的TIL(肿瘤浸润淋巴细胞)程度不同。MPM患者分离的PBMC中CXCL6和FOXJ1表达升高。
与SPM患者相比,MPM患者RFS和OS更差。MPM患者还存在免疫学差异,包括TIL含量以及PBMC中的CXCL6/FOXJ1表达变化,值得进一步研究。
Given equivocal results related to overall survival (OS) for patients with multiple primary melanomas (MPMs) compared with those with single primary melanomas (SPMs) in previous reports, the authors sought to determine whether OS differs between these 2 cohorts in their center using their UPCI-96-99 database. Secondary aims were to assess the differences in recurrence-free survival (RFS). In a subset of patients, transcriptomic profiling of peripheral blood mononuclear cells (PBMCs) was performed to assess disease-associated genes of interest.
This retrospective case-controlled study included patients with MPMs and age-, sex-, and stage-matched controls with SPMs at a 1:1 ratio. Cox regression models were used to evaluate the effect of the presence of MPMs on death and recurrence. NanoString PanCancer Immune Profiling was used to assess peripheral blood immune status in patients.
In total, 320 patients were evaluated. The mean patient age was 47 years; 43.8% were male. Patients with MPMs had worse RFS and OS (P = .023 and P = .0019, respectively). The presence of MPMs was associated with an increased risk of death (hazard ratio [HR], 4.52, P = .0006), and increased risk of disease recurrence (HR, 2.17; P = .004) after adjusting for age, sex, and stage. The degree of tumor-infiltrating lymphocytes (TILs) was different between the first melanoma of MPMs and SPMs. Expression of CXCL6 and FOXJ1 was increased in PBMCs isolated from patients with MPMs.
Patients with MPMs had worse RFS and OS compared with patients with SPMs. Immunologic differences were also observed, including TIL content and expression of CXCL6/FOXJ1 in PBMCs of patients with MPMs, which warrant further investigation.
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