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多中心随机 2 期 DIRECT 试验中,禁食模拟饮食作为乳腺癌新辅助化疗的辅助治疗。

Fasting mimicking diet as an adjunct to neoadjuvant chemotherapy for breast cancer in the multicentre randomized phase 2 DIRECT trial.

机构信息

Department of Medical Oncology, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The Netherlands.

Department of Pathology, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The Netherlands.

出版信息

Nat Commun. 2020 Jun 23;11(1):3083. doi: 10.1038/s41467-020-16138-3.

Abstract

Short-term fasting protects tumor-bearing mice against the toxic effects of chemotherapy while enhancing therapeutic efficacy. We randomized 131 patients with HER2-negative stage II/III breast cancer, without diabetes and a BMI over 18 kg m, to receive either a fasting mimicking diet (FMD) or their regular diet for 3 days prior to and during neoadjuvant chemotherapy. Here we show that there was no difference in toxicity between both groups, despite the fact that dexamethasone was omitted in the FMD group. A radiologically complete or partial response occurs more often in patients using the FMD (OR 3.168, P = 0.039). Moreover, per-protocol analysis reveals that the Miller&Payne 4/5 pathological response, indicating 90-100% tumor-cell loss, is more likely to occur in patients using the FMD (OR 4.109, P = 0.016). Also, the FMD significantly curtails chemotherapy-induced DNA damage in T-lymphocytes. These positive findings encourage further exploration of the benefits of fasting/FMD in cancer therapy. Trial number: NCT02126449.

摘要

短期禁食可保护荷瘤小鼠免受化疗的毒性作用,同时增强治疗效果。我们将 131 名 HER2 阴性 II/III 期乳腺癌患者、无糖尿病和 BMI 超过 18kg/m²的患者随机分为禁食模拟饮食(FMD)组或常规饮食组,在新辅助化疗前 3 天和化疗期间接受治疗。我们发现,尽管 FMD 组中省略了地塞米松,但两组之间的毒性没有差异。使用 FMD 的患者发生完全或部分缓解的比例更高(OR 3.168,P=0.039)。此外,根据方案分析,FMD 组患者更有可能出现 Miller&Payne 4/5 病理反应(表示 90-100%的肿瘤细胞丢失)(OR 4.109,P=0.016)。此外,FMD 显著减少了化疗诱导的 T 淋巴细胞中的 DNA 损伤。这些积极的发现鼓励进一步探索禁食/FMD 在癌症治疗中的益处。试验编号:NCT02126449。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e10d/7311547/7df3405b1823/41467_2020_16138_Fig1_HTML.jpg

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