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:Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Outcomes in histopathologic subgroups from the randomized, double-blind, phase 3 KEYNOTE-716 trial.
Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Outcomes in histopathologic subgroups from the randomized, double-blind, phase 3 KEYNOTE-716 trial.
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在这项事后分析中,无论组织病理学特征如何,pembrolizumab 的获益与总体研究人群基本一致。这些结果支持在已切除的 IIB 或 IIC 期黑色素瘤患者中使用辅助 pembrolizumab。
在针对已切除的IIB或IIC期黑色素瘤的3期KEYNOTE-716研究中,辅助帕博利珠单抗相比安慰剂显著改善了无复发生存期(RFS)和无远处转移生存期(DMFS)。在预设的第三次中期分析(数据截止日期为2022年1月4日)中,总体人群中RFS的HR为0.64(95% CI,0.50至0.84),DMFS的HR为0.64(95% CI,0.47至0.88)。我们按组织病理学特征定义的亚型进行了疗效的事后分析。
年龄≥12岁、新诊断且已切除的IIB或IIC期黑色素瘤患者被随机分配(1:1)接受帕博利珠单抗200 mg每3周一次(儿童患者为2 mg/kg,最高200 mg)或安慰剂。主要终点为研究者评估的RFS;研究者评估的DMFS为次要终点。关注的亚组包括黑色素瘤亚型(结节型 vs 非结节型)、肿瘤厚度(≤4 mm vs >4 mm)、是否存在溃疡(是 vs 否)、核分裂率(<5每mm²(中位数) vs ≥5每mm²),以及是否存在TIL(肿瘤浸润淋巴细胞)(TIL;无 vs 有)。
2018年9月23日至2020年11月4日期间,976例患者被分配至pembrolizumab组(n=487)或安慰剂组(n=489)。中位随访时间为27.4个月(范围,14.0-39.4)。RFS的HR(95% CI)在结节型黑色素瘤中为0.54(0.37至0.79),在非结节型黑色素瘤中为0.77(0.53至1.11);厚度≤4 mm为0.57(0.37至0.89),>4 mm为0.69(0.50至0.96);有溃疡为0.66(0.50至0.89),无溃疡为0.57(0.32至1.03);核分裂率<5每mm²为0.57(0.35至0.92),≥5每mm²为0.57(0.40至0.80);TILs缺失为0.89(0.52至1.54),TILs存在为0.51(0.34至0.76)。DMFS结果相似。在Cox多变量分析中,治疗组、肿瘤厚度和核分裂率是RFS的显著独立因素,治疗组和核分裂率是DMFS的显著独立因素。
Adjuvant pembrolizumab significantly improved recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) versus placebo in the phase 3 KEYNOTE-716 study of resected stage IIB or IIC melanoma. At the prespecified third interim analysis (data cut-off, January 4, 2022), the HR for RFS in the overall population was 0.64 (95% CI, 0.50 to 0.84) and the HR for DMFS was 0.64 (95% CI, 0.47 to 0.88). We present a post hoc analysis of efficacy by subtypes defined by histopathologic characteristics.
Patients aged ≥12 years with newly diagnosed, resected stage IIB or IIC melanoma were randomly assigned (1:1) to pembrolizumab 200 mg every 3 weeks (2 mg/kg up to 200 mg for pediatric patients) or placebo. The primary end point was RFS per investigator review; DMFS per investigator review was secondary. Subgroups of interest were melanoma subtype (nodular vs non-nodular), tumor thickness (≤4 mm vs >4 mm), presence of ulceration (yes vs no), mitotic rate (<5 per mm 2 (median) vs ≥5 per mm 2 ), and presence of tumor-infiltrating lymphocytes (TILs; absent vs present).
Between September 23, 2018, and November 4, 2020, 976 patients were assigned to pembrolizumab (n=487) or placebo (n=489). Median follow-up was 27.4 months (range, 14.0-39.4). The HR (95% CI) for RFS was 0.54 (0.37 to 0.79) for nodular and 0.77 (0.53 to 1.11) for non-nodular melanoma; 0.57 (0.37 to 0.89) for thickness ≤4 mm and 0.69 (0.50 to 0.96) for >4 mm; 0.66 (0.50 to 0.89) for ulceration and 0.57 (0.32 to 1.03) for no ulceration; 0.57 (0.35 to 0.92) for mitotic rate <5 per mm 2 and 0.57 (0.40 to 0.80) for ≥5 per mm 2 ; and 0.89 (0.52 to 1.54) for TILs absent and 0.51 (0.34 to 0.76) for TILs present. DMFS results were similar. In a Cox multivariate analysis, treatment arm, tumor thickness, and mitotic rate were significant independent factors for RFS, and treatment arm and mitotic rate were significant independent factors for DMFS.
In this post hoc analysis, the benefit of pembrolizumab was largely consistent with the overall study population regardless of histopathologic characteristics. These results support the use of adjuvant pembrolizumab in patients with resected stage IIB or IIC melanoma. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov, NCT03553836.
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