Fasting-Mimicking Diet Is Safe and Reshapes Metabolism and Antitumor Immunity in Patients with Cancer

医学 免疫系统 免疫 癌症 临床试验 药理学 癌症研究 髓系细胞 免疫学 细胞代谢 癌细胞 转录组 细胞 新陈代谢 髓样 药品 体外 肿瘤科 细胞免疫 内科学 外周血 相伴的 临床疗效 免疫疗法 先天免疫系统 毒性 外周血单个核细胞 血细胞 代谢活性
作者
Claudio Vernieri,Giovanni Fucà,Francesca Ligorio,Veronica Huber,Andrea Vingiani,Fabio Iannelli,Alessandra Raimondi,Darawan Rinchai,Gianmaria Frigè,Antonino Belfiore,Luca Lalli,Claudia Chiodoni,Valeria Cancila,Federica Zanardi,Arta Ajazi,Salvatore Cortellino,Viviana Vallacchi,Paola Squarcina,Agata Cova,Samantha Pesce
出处
期刊:Cancer Discovery [American Association for Cancer Research]
卷期号:12 (1): 90-107 被引量:286
标识
DOI:10.1158/2159-8290.cd-21-0030
摘要

In tumor-bearing mice, cyclic fasting or fasting-mimicking diets (FMD) enhance the activity of antineoplastic treatments by modulating systemic metabolism and boosting antitumor immunity. Here we conducted a clinical trial to investigate the safety and biological effects of cyclic, five-day FMD in combination with standard antitumor therapies. In 101 patients, the FMD was safe, feasible, and resulted in a consistent decrease of blood glucose and growth factor concentration, thus recapitulating metabolic changes that mediate fasting/FMD anticancer effects in preclinical experiments. Integrated transcriptomic and deep-phenotyping analyses revealed that FMD profoundly reshapes anticancer immunity by inducing the contraction of peripheral blood immunosuppressive myeloid and regulatory T-cell compartments, paralleled by enhanced intratumor Th1/cytotoxic responses and an enrichment of IFNγ and other immune signatures associated with better clinical outcomes in patients with cancer. Our findings lay the foundations for phase II/III clinical trials aimed at investigating FMD antitumor efficacy in combination with standard antineoplastic treatments. SIGNIFICANCE: Cyclic FMD is well tolerated and causes remarkable systemic metabolic changes in patients with different tumor types and treated with concomitant antitumor therapies. In addition, the FMD reshapes systemic and intratumor immunity, finally activating several antitumor immune programs. Phase II/III clinical trials are needed to investigate FMD antitumor activity/efficacy.This article is highlighted in the In This Issue feature, p. 1.
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