CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neoadjuvant chemotherapy enhances tumor-specific T cell immunity in patients with HPV-associated oropharyngeal cancer.
Neoadjuvant chemotherapy enhances tumor-specific T cell immunity in patients with HPV-associated oropharyngeal cancer.
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NAC 在新诊断的 HPV 相关 OPSCC 患者中诱导 HPV 特异性肿瘤 T 细胞反应;而 NAC 后未出现增加可能与复发风险相关。
新诊断的HPV相关口咽鳞状细胞癌(OPSCC)患者接受新辅助化疗(NAC)治疗,可获得较高的5年无复发生存率,且需要辅助治疗的患者较少。我们假设NAC增强了原发肿瘤的HPV特异性T细胞反应。
新辅助化疗前后TIL(肿瘤浸润淋巴细胞)(TILs)中的HPV特异性反应通过自体共培养试验测定。
在10例经PCR验证为HPV16阳性肿瘤的患者中,有8例(80%)在NAC后观察到比NAC前更强的HPV16特异性TIL反应,有时为多克隆反应。HPV特异性TIL反应的净负向变化与疾病复发之间存在显著关联(p = 0.04,Mann-Whitney检验),而手术时的病理完全缓解与复发无关。
Treatment of patients with newly diagnosed HPV-associated oropharyngeal squamous cell carcinoma (OPSCC) with neoadjuvant chemotherapy (NAC) results in a high rate of 5-year recurrence free survival with few patients requiring adjuvant treatment. We hypothesized that NAC enhances primary tumor HPV-specific T cell responses.
HPV-specific responses in tumor infiltrating lymphocytes (TILs) before and after NAC were determined using autologous co-culture assays.
Greater HPV16-specific TIL responses, sometimes polyclonal, were observed after NAC compared to before in 8 of 10 patients (80%) with PCR-verified HPV16-positive tumors. A significant association was observed between net-negative change in HPV-specific TIL response and disease relapse (p = 0.04, Mann-Whitney test), whereas pathologic complete response at time of surgery did not correlate with recurrence.
NAC induces HPV-specific tumor T cell responses in patients with newly diagnosed HPV-associated OPSCC; whereas lack of an increase following NAC may associate with risk of relapse.
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