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:Incorporating weekly carboplatin in anthracycline and paclitaxel-containing neoadjuvant chemotherapy for triple-negative breast cancer: propensity-score matching analysis and TIL evaluation.
Incorporating weekly carboplatin in anthracycline and paclitaxel-containing neoadjuvant chemotherapy for triple-negative breast cancer: propensity-score matching analysis and TIL evaluation.
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我们在接受 A-T NACT 的 TNBC 患者临床实践环境中证实,加入每周 Cb 显著改善了 pCR。此外,A-T +/- Cb 增强了从基线到 RD 的免疫浸润。最后,我们报告了 NACT 暴露后 TIL 增加具有积极的独立预后作用。
在临床实践环境中,迫切需要生成数据以捕捉将卡铂(Cb)纳入三阴性乳腺癌(TNBC)新辅助化疗(NACT)的风险-获益比。TIL(肿瘤浸润淋巴细胞)(TILs)在接受NACT的TNBC中已确立作用,然而,在接受当前标准治疗的患者中,NACT暴露下TIL动态的作用在很大程度上尚未被探索。
连续入组了三家机构接受蒽环类-紫杉类[A-T]±Cb NACT的TNBC患者。在NACT前和残留病灶(RD)标本上评估了基质TILs。在临床队列中,使用倾向性评分匹配来控制选择偏倚。
共纳入247例患者(A-T = 40.5%,A-TCb = 59.5%)。经倾向性评分匹配后,A-TCb 相比 A-T 的 pCR 显著更高(51.9% vs 34.2%,多因素分析:OR = 2.40,P = 0.01)。未观察到3级血液学毒性方面的差异。在总体人群及 A-T/A-TCb 各亚组中,TILs 从基线到 RD 均有所增加。TIL 从基线到 RD 的增加与远处无病生存期呈正向且独立相关(多因素分析:HR = 0.43,P = 0.05)。
The generation of data capturing the risk-benefit ratio of incorporating carboplatin (Cb) to neoadjuvant chemotherapy (NACT) for triple-negative breast cancer (TNBC) in a clinical practice setting is urgently needed. Tumour-infiltrating lymphocytes (TILs) have an established role in TNBC receiving NACT, however, the role of TIL dynamics under NACT exposure in patients receiving the current standard of care is largely uncharted.
Consecutive TNBC patients receiving anthracycline-taxane [A-T] +/- Cb NACT at three Institutions were enrolled. Stromal-TILs were evaluated on pre-NACT and residual disease (RD) specimens. In the clinical cohort, propensity-score-matching was used to control selection bias.
In total, 247 patients were included (A-T = 40.5%, A-TCb = 59.5%). After propensity-score-matching, pCR was significantly higher for A-TCb vs A-T (51.9% vs 34.2%, multivariate: OR = 2.40, P = 0.01). No differences in grade 3 haematological toxicities were observed. TILs increased from baseline to RD in the overall population and across A-T/A-TCb subgroups. TIL increase from baseline to RD was positively and independently associated with distant disease-free survival (multivariate: HR = 0.43, P = 0.05).
We confirmed in a clinical practice setting of TNBC patients receiving A-T NACT that the incorporation of weekly Cb significantly improved pCR. In addition, A-T +/- Cb enhanced immune infiltration from baseline to RD. Finally, we reported a positive independent prognostic role of TIL increase after NACT exposure.
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