CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Tumor Hypoxia and CD8(+) T-Cell Infiltration in Patients With Advanced Laryngeal Cancer.
Tumor Hypoxia and CD8(+) T-Cell Infiltration in Patients With Advanced Laryngeal Cancer.
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CAIX 染色与接受 bioselection 的晚期喉鳞状细胞癌患者中 CD8⁺ T 细胞浸润减少相关。
在采用生物学选择策略接受根治性治疗的晚期喉鳞状细胞癌患者队列中,评估肿瘤碳酸酐酶IX(CAIX)染色(作为肿瘤缺氧标志物)与CD8+ T细胞浸润之间的相关性。研究设计:回顾性队列研究。研究地点:三级医疗中心。
纳入按照生物学选择治疗模式接受治疗的III至IV期喉鳞状细胞癌患者。对CD8+ T细胞和CAIX进行免疫组织化学染色。采用非参数检验和Kaplan-Meier生存分析,比较CAIX状态与临床病理变量及CD8+ T细胞浸润的关系,并评估CAIX以及CAIX与TIL(肿瘤浸润淋巴细胞)联合分组对生存的影响。
队列共纳入92例患者,其中68例(73.9%)为声门上型肿瘤。不同肿瘤亚部位、分期及诱导化疗应答患者之间的CAIX染色无差异(均P>0.05)。13例肿瘤(14.1%)CAIX阳性,其CD8+ T细胞浸润显著低于CAIX阴性肿瘤[18(0–62)对32(0–399),P=0.028]。CAIX/TIL联合分组与应答可能性显著相关(CAIX阴性/TIL高者应答可能性较低);在应答者中,该分组还能预测更大程度的肿瘤缩小(>80%)。
接受生物学选择治疗的晚期喉鳞癌患者中,CAIX染色与CD8+ T细胞浸润减少相关。CAIX/TIL联合分组与诱导治疗的应答可能性及应答程度相关。CAIX状态及其他免疫与缺氧联合特征作为诱导治疗应答和生存生物标志物的效用,仍需前瞻性评估。
We assessed correlations between tumor carbonic anhydrase IX (CAIX) staining, as a marker of tumor hypoxia, and CD8 + T-cell infiltration in a cohort of patients with advanced laryngeal squamous cell carcinoma undergoing a bioselection approach for definitive treatment. STUDY DESIGN: Retrospective cohort study. SETTING: Tertiary care hospital.
Patients with stage III to IV laryngeal squamous cell carcinoma treated under a bioselection paradigm were included. Immunohistochemistry for CD8 + T-cells and CAIX was performed. Nonparametric tests and Kaplan-Meier survival analyses were used to compare tumor CAIX status by clinicopathologic variables and CD8 + T-cell infiltration and to evaluate the role of CAIX and combination CAIX/tumor infiltrating lymphocytes (TIL) category on survival.
Our cohort included 92 patients (n = 68 [73.9%] supraglottic). No difference in CAIX staining was seen by tumor subsite, stage, and response to induction chemotherapy (all P > .05). Thirteen (14.1%) tumors were CAIX-positive and showed significantly lower CD8 + T-cell infiltration than CAIX-negative tumors (18 [0-62] vs 32 [0-399], P = .028). Combination CAIX/TIL category was significantly associated with the likelihood of response (CAIX-/TIL[high] were less likely to respond) and in the group of responders, was predictive of a higher degree of tumor shrinkage (>80%).
CAIX staining correlates with reduced CD8 + T-cell infiltration in patients with advanced laryngeal squamous cell carcinoma undergoing bioselection. The combination CAIX/TIL category is associated with the likelihood and degree of response to induction. The utility of CAIX status and other combination immune and hypoxia signatures as a biomarker of induction response and survival merits prospective evaluation.
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