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.
过继性自然杀伤(NK)细胞疗法是治疗三阴性乳腺癌的一种有前景的策略,但其疗效往往受到瘤内持久性差以及在免疫抑制性肿瘤微环境中功能耗竭的限制。
英文原题:Evaluation of tumor infiltrating lymphocytes as a prognostic biomarker in patients with ductal carcinoma in situ of the breast.
Evaluation of tumor infiltrating lymphocytes as a prognostic biomarker in patients with ductal carcinoma in situ of the breast.
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在我们的队列中,高比例的 TILs(17%)和粉刺样坏死的存在与 DCIS 复发独立相关。
评估导管原位癌(DCIS)样本中TIL(肿瘤浸润淋巴细胞)(TILs)与疾病复发之间的关联。
这项回顾性队列研究纳入了2007年1月至2020年12月期间接受治疗的18岁及以上女性。排除男性患者、根据手术标本解剖病理学检查诊断为浸润性或微浸润性疾病的个体,以及有任何人其他癌症个人史的患者。此外,评估了“接触性TILs”(与肿瘤细胞直接接触的淋巴细胞)和导管周围促纤维增生作为代表免疫微环境的补充方法。主要结局是基于TIL定量并针对潜在混杂因素进行调整后的无复发生存期。病理学家在肿瘤代表性最高的样本中评估TILs,并以百分比进行量化。使用Kaplan Meier曲线、log-rank检验和Cox回归模型评估生存。
共191例患者符合纳入标准。平均随访时间为77.2个月,复发率为9.2%。TILs 17%的患者复发风险更高(HR 2.97,95% CI 1.17-7.51;p = 0.02)。此外,局灶性坏死(HR 6.4,95% CI 1.39-34.71;p = 0.018)或粉刺样坏死(HR 4.53,95% CI 1.34-15.28;p = 0.015)与复发风险增加相关。根据多因素模型,粉刺样坏死和TILs 17%与复发显著相关(分别为p = 0.034和p = 0.035)。关于“接触性TILs”和管周促结缔组织增生反应的评估,在分析其与疾病复发的关联时未发现统计学显著性。
To assess the association between tumor-infiltrating lymphocytes (TILs) in ductal carcinoma in situ (DCIS) samples and disease recurrence.
This retrospective cohort study included women aged 18 years and older who underwent treatment between January 2007 and December 2020. Male patients, individuals diagnosed with invasive or microinvasive disease based on anatomopathological examination of surgical specimens, and those with a personal history of any other cancers were excluded. Additionally, the presence of "touching TILs" (lymphocytes in direct contact with tumor cells) and periductal desmoplasia were evaluated as complementary methods to represent the immunological microenvironment. The primary outcome was relapse-free survival based on TIL quantification adjusted for potential confounders. Pathologists assessed TILs in the sample with the highest tumor representation and quantified them as a percentage. Survival was evaluated using Kaplan Meier curves, log-rank tests, and Cox regression models.
A total of 191 patients met the eligibility criteria. The mean follow-up duration was 77.2 months, with a recurrence rate of 9.2%. Patients with TILs 17% had a greater risk of recurrence (HR 2.97, 95% CI 1.17-7.51; p = 0.02). Additionally, focal necrosis (HR 6.4, 95% CI 1.39-34.71; p = 0.018) or comedonecrosis (HR 4.53, 95% CI 1.34-15.28; p = 0.015) were associated with increased recurrence risk. According to the multivariate model, comedonecrosis and TILs 17% were significantly associated with recurrence (p = 0.034 and p = 0.035, respectively). Regarding the evaluations of "touching TILs" and periductal desmoplasia, no statistical significance was found when assessing their association with disease recurrence.
In our cohort, a high percentage of TILs ( 17%) and the presence of comedonecrosis were independently associated with DCIS recurrence.
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