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:Tumor infiltrating lymphocytes in primary melanoma are associated with a better prognosis.
Tumor infiltrating lymphocytes in primary melanoma are associated with a better prognosis.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
TIL 对黑色素瘤的生存具有强烈预测作用,在决定某些患者辅助治疗的风险是否大于获益时,可能有助于风险分层。
TIL(肿瘤浸润淋巴细胞)与黑色素瘤生存之间的关系尚不明确。我们开展了一项大型多中心研究,评估TIL与生存之间的关联。
前哨淋巴结工作组数据库查询了1993年至2024年间具有已知TIL和生存数据的病例。TIL以二分法分析,并分层为非活跃、活跃和缺失。临床病理因素与黑色素瘤特异性生存期(MSS)、总生存期(OS)和无复发生存期(RFS)相关。
在4957例患者中,3980例(80.2%)存在TIL。TIL对MSS(p = 0.0033)、OS(p = 0.0053)和RFS(p = 0.0011)具有预后意义。在分层分析中,brisk TIL与MSS、OS和RFS的关联比non-brisk TIL更强(所有p < 0.04)。在前哨淋巴结阳性的患者中,TIL对MSS、OS和RFS具有预后意义(所有p < 0.03)。
The relationship between tumor infiltrating lymphocytes (TIL) and survival in melanoma is poorly understood. We present a large multicenter study assessing the association between TIL and survival.
The Sentinel Lymph Node Working Group database was queried from 1993 to 2024 for cases with known TIL and survival data. TIL was analyzed dichotomously and stratified as non-brisk, brisk, and absent. Clinicopathologic factors were correlated with melanoma-specific survival (MSS), overall survival (OS), and recurrence-free survival (RFS).
Among 4957 patients, TIL was present in 3980 (80.2 %) of patients. TIL was prognostic of MSS (p = 0.0033), OS (p = 0.0053), and RFS (p = 0.0011). In the stratified analysis, brisk TIL was more strongly associated with MSS, OS, and RFS than non-brisk TIL (all p < 0.04). Among patients with a positive sentinel lymph node, TIL was prognostic of MSS, OS, and RFS (all p < 0.03).
TIL is strongly predictive of survival in melanoma and may be useful in risk stratification when deciding whether risks of adjuvant therapy outweigh benefits for certain patients.
MEMBER ACCOUNT
登录成功会直接打开下一页。