下一代肿瘤不可知靶点即将出现
Next-generation tumor-agnostic targets on the horizon.
肿瘤不可知药物开发将肿瘤学重新聚焦于共享的分子依赖性而非组织来源,从而能够针对跨肿瘤的罕见可操作驱动因素进行高效开发。
英文原题:Case Report: Prognostic evaluation of immunotherapy in two patients with SMARCA4-UT using TCR as a new marker.
胸部SMARCA4缺陷型未分化肿瘤(SMARCA4-UT)是新近分类的非小细胞肺癌(NSCLC)亚组,较为罕见且与不良预后相关。
胸部SMARCA4缺陷型未分化肿瘤(SMARCA4-UT)是新近分类的非小细胞肺癌(NSCLC)亚型,较为罕见且预后不佳。关于其治疗选择和预后评估,目前缺乏有力研究。通常,SMARCA4相关NSCLC患者的一线治疗与软组织肉瘤(STS)类似。STS对化疗部分不敏感,且缺乏特异性靶向治疗。因此,免疫治疗日益被用于一线治疗。本文介绍了两例SMARCA4患者接受化疗联合免疫治疗的过程,并采用T细胞受体测序(TCR-seq)技术。从免疫微环境角度出发,作者提出TCR这一新的潜在标志物,可能用于评估SMARCA4患者免疫治疗的预后,并从组织免疫和外周免疫两个方面提供理论依据。
Thoracic SMARCA4-deficient undifferentiated tumour(SMARCA4-UT) is a newly classified subgroup of non-small cell lung cancer (NSCLC) that is rare and associated with a poor prognosis. There is a paucity of robust research regarding its treatment options and prognostic assessment. Generally, the first-line treatments for NSCLC patients with SMARCA4 are similar to those for soft tissue sarcoma (STS). STS is partially insensitive to chemotherapy and lacks specific targeted therapeutic interventions. Consequently, the immunotherapy is increasingly applied as the first-line treatment. This paper described the treatment process of two SMARCA4 patients receiving a combination of chemotherapy and immunotherapy, employing T-cell Receptor-sequencing technology(TCR). From the perspective of the immune microenvironment, we propose a novel potential marker-TCR-that may serve as an indicator for prognostic evaluation of immunotherapy in SMARCA4 patients, thereby providing a theoretical foundation from the perspectives of tissue and peripheral immunity.
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