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:Concurrent Neoadjuvant Chemotherapy and Radiation in Locally Advanced Breast Cancer: Impact on Locoregional Recurrence Rates.
Concurrent Neoadjuvant Chemotherapy and Radiation in Locally Advanced Breast Cancer: Impact on Locoregional Recurrence Rates.
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新辅助放化疗(NCRT)在乳腺癌中是一种未被充分利用的治疗方法,但可能通过影响肿瘤免疫微环境来改善预后。本研究的目的是评估NCRT对复发的影响以及TIL(肿瘤浸润淋巴细胞)(TILs)在治疗反应中的作用。
我们假设NCRT通过上调TILs来减少复发。局部晚期乳腺癌(LABC)患者接受NCRT治疗。任何分子亚型的IIB至III期患者均符合条件。通过倾向性评分将患者按年龄、分期和分子亚型与同期接受标准新辅助化疗(NCT)后辅助放疗的队列进行匹配。
本研究的目的是评估患者的病理完全缓解(pCR)、治疗前后TIL计数以及局部区域复发。中位随访时间为7.2年。30例NCRT患者成功按1:3匹配至90例NCT患者。NCRT队列无区域复发和局部区域复发(分别为 p = 0.036,风险比 HR [0.25],95% 置信区间 CI [0.06-0.94] 和 p = 0.013,HR [0.25],95% CI [0.08-0.76]),而NCT队列为17.8%。NCRT组的pCR显著更多,且治疗后pCR标本中TILs增加。NCRT可以改善LABC患者的预后,具有更高的pCR和显著更低的局部区域复发/更高的无复发生存率。需要进一步试验来评估NCRT在所有乳腺癌患者中的作用。
Neoadjuvant chemoradiation therapy (NCRT) is an underutilized treatment in breast cancer but may improve outcomes by impacting the tumor immune microenvironment. The aim of this study was to evaluate NCRT's impact on recurrence and the role of tumor-infiltrating lymphocytes (TILs) in treatment response.
We hypothesized that NCRT reduces recurrence by upregulating TILs. Patients with locally advanced breast cancer (LABC) were treated with NCRT. Stage IIB to III patients with any molecular subtypes were eligible. The patients were matched for age, stage, and molecular subtype by a propensity score to a concurrent cohort receiving standard neoadjuvant chemotherapy (NCT) followed by adjuvant radiation. The objective of this study was to assess the patients in terms of the pathological complete response (pCR), TIL counts prior to and following treatment, and locoregional recurrence.
The median follow-up was 7. 2 years. Thirty NCRT patients were successfully matched 1:3 to ninety NCT patients. The NCRT cohort had no regional and locoregional recurrences ( p = 0. 036, (hazard ratio) HR [0. 25], 95% confidence interval (CI) [0. 06-0. 94] and p = 0. 013, HR [0. 25], 95% CI [0. 08-0.
76], respectively), compared to 17. 8% of the NCT cohort. The NCRT group had significantly more pCRs, and TILs were increased in the post-treatment pCR specimens. NCRT can improve outcomes in LABC patients, with a higher pCR and significantly lower locoregional recurrence/higher recurrence-free survival.
Further trials are needed to evaluate the role of NCRT in all breast cancer patients.
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