PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Postoperative dendritic cell vaccination in brain metastasis: A real-world retrospective cohort study evaluating survival and safety.
Postoperative dendritic cell vaccination in brain metastasis: A real-world retrospective cohort study evaluating survival and safety.
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脑转移(BM)与不良预后和治疗选择有限相关。树突状细胞(DC)疫苗免疫治疗是一种有前景的方法,可能克服血脑屏障的限制,同时产生肿瘤特异性免疫应答。
本研究评估术后DC疫苗接种在手术切除BM患者中的安全性和初步疗效。我们进行了一项回顾性分析,纳入17例(9例女性,8例男性;平均年龄:56.2岁)来自不同原发癌种的BM患者,他们在2019年至2022年间于单一机构接受了常规治疗加自体DC疫苗接种。肿瘤切除后,患者在6个月内接受放疗和/或全身治疗,同时接受DC疫苗接种(皮下注射2 × 108 DCs)。评估患者的不良事件、总生存期(OS),以及相对于基于诊断特异性分级预后评估(DS-GPA)的预后预期的生存情况。中位OS为18个月(95% CI:9-22),而单纯手术切除的历史中位数为14.5个月。接受≥ 6剂疫苗的患者中位OS为18个月(95% CI:9-24),而接受< 6剂的患者为17个月(95% CI:3-24)(Log-rank检验,P = .39)。在14例有可用DS-GPA评分的患者中,9例(64.3%)的生存时间长于其预测中位生存期。未观察到与疫苗相关的严重不良事件,反应仅限于1级注射部位反应和低热。这项真实世界分析表明,BM术后DC疫苗接种是安全的,并且与历史结局相比可能带来生存获益。尽管受样本量和回顾性设计的限制,我们的发现值得在前瞻性对照试验中进一步研究,以明确确立疗效及其在多模式治疗方法中的最佳整合。
Brain metastasis (BM) is associated with poor prognosis and limited therapeutic options. Immunotherapy with dendritic cell (DC) vaccination represents a promising approach by potentially overcoming blood-brain barrier limitations while generating tumor-specific immune responses.
This study evaluates the safety and preliminary efficacy of postoperative DC vaccination in patients with surgically resected BMs.
We conducted a retrospective analysis of 17 patients (9 women, 8 men; mean age: 56. 2 years) with BM from diverse primary cancers who received conventional treatment plus autologous DC vaccination between 2019 and 2022 at a single institution. Following tumor resection, patients received radiotherapy and/or systemic therapy alongside DC vaccination (2 × 108 DCs administered subcutaneously) over 6 months. Patients were assessed for adverse events, overall survival (OS), and survival relative to prognostic expectations based on diagnosis-specific graded prognostic assessment (DS-GPA). The median OS was 18 months (95% CI: 9-22), compared to historical median of 14. 5 months for surgical resection alone.
Patients receiving ≥ 6 vaccine doses demonstrated a median OS of 18 months (95% CI: 9-24) versus17 (95% CI: 3-24) for those receiving < 6 doses (Log-rank test, P = . 39). Among 14 patients with available DS-GPA scores, 9 (64. 3%) survived longer than their predicted median survival. No vaccine-related serious adverse events were observed, with reactions limited to grade 1 injection site reactions and low-grade fever.
This real-world analysis suggests that postoperative DC vaccination for BM is safe and may confer survival benefit compared to historical outcomes. While limited by sample size and retrospective design, our findings warrant further investigation in prospective controlled trials to definitively establish efficacy and optimal integration into multimodal treatment approaches.
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