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

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          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 −2, 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.

          Abstract

          Preclinical evidence suggests that a fasting mimicking diet (FMD) can make cancer cells more vulnerable to chemotherapy, while protecting normal cells. In this randomized phase II clinical trial of 131 patients with HER2 negative early stage breast cancer, the authors demonstrate that FMD is safe and enhances the effects of neoadjuvant chemotherapy on radiological and pathological tumor response.

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          A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival.

          The clinical and complete pathological response of a primary breast cancer to chemotherapy has been shown to be an important prognostic for survival. However, the majority of patients do not experience a complete pathological response to primary chemotherapy and the significance of lesser degrees of histological response is uncertain and the prognostic significance is unknown. The purpose of this study was to evaluate a new histological grading system to assess response of breast cancers to primary chemotherapy and to determine if such a system has prognostic value.A consecutive series of 176 patients with large (> or =4cm) and locally advanced breast cancers were treated with multimodality therapy comprising primary chemotherapy, surgery, radiotherapy and tamoxifen. All underwent assessment of the primary breast tumour before and after completion of chemotherapy. Residual tumour was excised after completion of chemotherapy (mastectomy or wide local excision with axillary surgery). The removed tissue was assessed and response to chemotherapy graded using a five-point histological grading system based with the fundamental feature being a reduction in tumour cellularity; comparison being made with a pre-treatment core biopsy. All patients were followed up for 5 years or more. Pathological responses were compared to 5 year overall survival and disease-free survival using log rank tests. The overall 5-year survival for all patients was 71%, and 5 year disease free interval was 60%. There was a significant correlation between pathological response using this new grading system and both overall survival (P=0.02) and disease-free interval (P=0.04). In a multivariate analysis of known prognostic factors, the Miller/Payne grading system was an independent predictor of overall patient survival. This grading system, which assesses the histological response to primary chemotherapy, can predict overall survival and disease-free interval in patients with large and locally advanced breast cancers treated with such therapy. The relationship of degree of histological response to overall and disease-free survival has been shown in univariate and multivariate analyses and could potentially have an important role in the clinical management of patients with locally advanced breast cancer undergoing primary chemotherapy.
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            Nutritional regulation of the insulin-like growth factors.

            Nutrition is one of the main regulators of circulating IGF-I. In humans, serum IGF-I concentrations are markedly lowered by energy and/or protein deprivation. Both energy and proteins are critical in the regulation of serum IGF-I concentrations. Indeed, after fasting, optimal intake of both energy and protein is necessary for the rapid restoration of circulating IGF-I. We believe, however, that in adult humans energy may be somewhat more important than protein in this regard. While the lowest protein intake is able to increase IGF-I in the presence of adequate energy, there is a threshold energy requirement below which optimal protein intake fails to raise IGF-I after fasting. When energy intake is severely reduced, the carbohydrate content of the diet is a major determinant of responsiveness of IGF-I to GH. The essential amino acid content of the diet is also critical for the optimal restoration of IGF-I after fasting, when protein intake is reduced. The exquisite sensitivity of circulating IGF-I to nutrients, the nycthemeral stability of its concentrations and its relative short half-life constitute the basis for its use as a marker of both nutritional status and adequacy of nutritional rehabilitation. For these indications, IGF-I measurement is more sensitive and more specific than measurement of the other nutrient-related serum proteins (albumin, prealbumin, transferrin, retinol-binding protein). Animal models have been developed to investigate the mechanisms responsible for the nutritional regulation of IGF-I. There is no doubt that many mechanisms are involved (Fig. 12). Decline of serum IGF-I in dietary restriction is independent of the diet-induced alterations in pituitary GH secretion. The role of the liver GH receptors is dependent on the severity of the nutritional insult. In severe dietary restriction (fasting), a marked decrease of the number of somatogenic receptors supports the role of a receptor defect in the decline of circulating IGF-I. In contrast, in less severe forms of dietary restriction (protein restriction), the decline of IGF-I results from a postreceptor defect in the GH action at the hepatic level. Nutritional deprivation decreases hepatic IGF-I production by diminishing IGF-I gene expression. Decline in IGF-I gene expression is mainly caused by nutrient deficiency and less importantly by the nutritionally induced hormonal changes (insulin and T3). Diet restriction also increases the clearance and degradation of serum IGF-I through changes in the levels of circulating IGFBPs.(ABSTRACT TRUNCATED AT 400 WORDS)
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              A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival

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                Author and article information

                Contributors
                j.r.kroep@lumc.nl
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                23 June 2020
                23 June 2020
                2020
                : 11
                : 3083
                Affiliations
                [1 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Medical Oncology, , Leiden University Medical Center, ; P.O. Box 9600, 2300 RC Leiden, The Netherlands
                [2 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Pathology, , Leiden University Medical Center, ; P.O. Box 9600, 2300 RC Leiden, The Netherlands
                [3 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Human Genetics, , Leiden University Medical Center, ; P.O. Box 9600, 2300 RC Leiden, The Netherlands
                [4 ]ISNI 0000 0004 0419 3743, GRID grid.414846.b, Department of Medical Oncology, , Medical center Leeuwarden, ; P.O. Box 888, 8901 NR Leeuwarden, The Netherlands
                [5 ]GRID grid.413711.1, Department of Medical Oncology, , Amphia, ; P.O. Box 90157, 4800 RL Breda, The Netherlands
                [6 ]ISNI 0000 0004 0568 6689, GRID grid.413591.b, Department of Medical Oncology, , Haga hospital, ; P.O. Box 40551, 2504 LN Den Haag, The Netherlands
                [7 ]ISNI 0000 0004 0477 5022, GRID grid.416856.8, Department of Medical Oncology, , Viecuri, ; 5912BL Venlo, The Netherlands
                [8 ]ISNI 0000 0004 0396 5908, GRID grid.413649.d, Department of Medical Oncology, , Deventer hospital, ; P.O. Box 5001, 7416 SE Deventer, The Netherlands
                [9 ]Department of Medical Oncology, Noordwest hospital group, location Alkmaar, P.O. Box 501, 1815 JD Alkmaar, The Netherlands
                [10 ]ISNI 0000 0004 0398 026X, GRID grid.415351.7, Department of Medical Oncology, , Hospital Gelderse vallei, ; 6710 HN Ede, The Netherlands
                [11 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Surgery, , Leiden University Medical Center, ; P.O. Box 9600, 2300 RC Leiden, The Netherlands
                [12 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Medical Statistics and Bioinformatics, , Leiden University Medical Center, ; P.O. Box 9600, 2300RC Leiden, The Netherlands
                [13 ]ISNI 0000 0001 2156 6853, GRID grid.42505.36, Longevity Institute, School of Gerontology, and Department of Biological Sciences, , University of Southern California, ; Los Angeles, CA 90089 USA
                [14 ]ISNI 0000 0004 1757 7797, GRID grid.7678.e, IFOM FIRC Institute of Molecular Oncology, ; Via Adamello 16, Milan, Italy
                [15 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Endocrinology, , Leiden University Medical Center, ; P.O. Box 9600, 2300 RC Leiden, The Netherlands
                [16 ]GRID grid.476173.0, BOOG Study Center, ; P.O. Box 9236, 1006 AE Amsterdam, The Netherlands
                [17 ]Department of Medical Oncology, Alexander Monro Hospital, 3723 MB Bilthoven, The Netherlands
                [18 ]Department of Medical Oncology, ‘t Langeland Hospital, 2725 NA Zoetermeer, The Netherlands
                [19 ]ISNI 0000 0001 0547 5927, GRID grid.452600.5, Department of Medical Oncology, , Isala hospital, ; 8025 AB Zwolle, The Netherlands
                Author information
                http://orcid.org/0000-0002-9809-8266
                http://orcid.org/0000-0003-4068-9271
                http://orcid.org/0000-0002-1750-2221
                http://orcid.org/0000-0002-0946-7534
                http://orcid.org/0000-0002-3076-1551
                http://orcid.org/0000-0003-2671-1903
                Article
                16138
                10.1038/s41467-020-16138-3
                7311547
                32576828
                d947c918-7011-4e03-af5a-34ce9305911d
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 17 December 2019
                : 14 April 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/100010806, Amgen Inc. | Amgen Nederland (Amgen B.V. Netherlands);
                Award ID: 20139098
                Award Recipient :
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                © The Author(s) 2020

                Uncategorized
                breast cancer,chemotherapy
                Uncategorized
                breast cancer, chemotherapy

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