基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:High tumor expression of CTLA4 identifies lymph node-negative basal-like breast cancer patients with excellent prognosis.
High tumor expression of CTLA4 identifies lymph node-negative basal-like breast cancer patients with excellent prognosis.
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CTLA4 的原发肿瘤高表达表明患者预后良好,对这些患者来说标准化疗可能会降低或省略。大多数乳腺癌患者在初次手术和放射治疗后即可治愈。然而,基底样乳腺癌约占病例的 15%,具有很高的早期复发和死亡风险。因此,几乎所有基底样乳腺癌患者在手术前后都会接受额外的治疗,包括化疗和免疫治疗。这种治疗降低了复发风险,但会引起相当大的短期和长期副作用。在目前的研究中,我们发现肿瘤中免疫相关基因 CTLA4 水平高的患者预后良好,可能是因为免疫系统有助于对抗癌症。
肿瘤免疫细胞浸润是三阴性乳腺癌的有利预后因素。大多数三阴性肿瘤属于侵袭性基底细胞样亚型。我们假设免疫基因表达可能会识别出可以降低辅助化疗的低风险患者。
对 45 名患有基底样疾病且无淋巴结转移的患者(Oslo1 队列)的肿瘤活检样本中 753 个免疫相关基因的表达进行了分析,并评估了预后价值。研究结果在两个独立队列中得到了验证。 Oslo1 活检还分析了TIL(肿瘤浸润淋巴细胞)和三级淋巴结构 (TLS)。
在这里,我们表明 CTLA4 的高表达(高于 63%)与 Oslo1 队列中的良好预后相关。 CTLA4 高组中没有患者出现疾病复发(中位随访 7.4 年)或乳腺癌相关死亡(中位随访 17.7 年)。对 SCAN-B(n = 233;CTLA4 高组中 97% 无远处复发)和 METABRIC 队列(n = 155;CTLA4 高组中 93% 疾病特异性生存率)的分析验证了这一发现,这也适用于未接受化疗的患者。 CTLA4 表达与 TIL 评分和 TLS 水平相关(Oslo1 队列),但没有 TIL 低/CTLA4 高患者死于乳腺癌,这表明 CTLA4 读数可识别 TIL 评估未捕获的低风险患者。
Tumor immune cell infiltration is a favorable prognostic factor in triple-negative breast cancer. Most triple-negative tumors belong to the aggressive basal-like subtype. We hypothesized that immune gene expression may identify low-risk patients for whom adjuvant chemotherapy can be de-escalated.
The expression of 753 immune-related genes was analyzed in tumor biopsies from 45 patients with basal-like disease and no lymph node metastases (Oslo1 cohort) and evaluated for prognostic value. Findings were validated in two independent cohorts. Oslo1 biopsies were also analyzed for tumor-infiltrating lymphocytes (TIL) and tertiary lymphoid structures (TLS).
Here we show that a high expression of CTLA4 (above 63 rd percentile) is associated with an excellent prognosis in the Oslo1 cohort. None of the patients in the CTLA4 high group suffered disease recurrence (median follow-up 7.4 years) or breast cancer-related death (median follow-up 17.7 years). Analysis of the SCAN-B (n = 233; 97% without distant recurrence in CTLA4 high group) and METABRIC cohorts (n = 155; 93% disease-specific survival in CTLA4 high group) validates this finding, which also applies to patients who did not receive chemotherapy. CTLA4 expression correlates with TIL score and TLS levels (Oslo1 cohort), but no TIL low /CTLA4 high patients died from breast cancer, suggesting that the CTLA4 readout identifies low-risk patients not captured by TIL assessment.
A high primary tumor expression of CTLA4 identifies patients with an excellent prognosis, for whom standard chemotherapy may be de-escalated or omitted. Most breast cancer patients are cured after the initial surgery and radiotherapy. However, basal-like breast cancer, which makes up about 15% of cases, carries a high risk of early recurrence and death. Nearly all patients with basal-like breast cancer therefore receive additional treatment before and after surgery, including chemotherapy and immunotherapy. This treatment reduces the risk of recurrence but causes considerable short- and long-term side effects. In the current study, we found that patients with high levels of the immune-related gene CTLA4 in tumor had an excellent prognosis, likely because the immune system aids in fighting the cancer. Our findings suggest that the additional treatments given to some patients may safely be omitted or reduced, which could improve the quality of life of cancer survivors.
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