Exploiting FAsting-mimicking Diet and MEtformin to Improve the Efficacy of Platinum-pemetrexed Chemotherapy in Advanced LKB1-inactivated Lung Adenocarcinoma: The FAME Trial.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
05 2019
Historique:
received: 24 09 2018
revised: 02 12 2018
accepted: 10 12 2018
pubmed: 9 1 2019
medline: 4 4 2020
entrez: 9 1 2019
Statut: ppublish

Résumé

Advanced lung adenocarcinoma with inactive liver kinase B1 (LKB1) tumor suppressor protein is associated with poor response to immune checkpoint inhibitors and molecularly targeted agents, and with dismal patient prognosis. LKB1 is a central orchestrator of cancer cell metabolism, and halts tumor growth/proliferation during metabolic stress. Recent preclinical evidence suggests that LKB1-inactive lung adenocarcinoma is highly sensitive to metformin, a safe and low-cost antidiabetic compound that inhibits mitochondrial oxidative phosphorylation. The effects of metformin can be enhanced by nutrient deprivation (ie, glucose, amino acids), which reduces intracellular levels of ATP and anabolic precursors and can be achieved by the fasting mimicking diet (FMD). Noticeably, metformin also prevents resistance to cisplatin in preclinical in vitro and in vivo models of LKB1-inactive lung adenocarcinoma. Based on such preclinical evidence, the phase II FAME trial was designed to test the hypothesis that the addition of metformin, with or without cyclic FMD, to standard platinum-based chemotherapy improves the progression-free survival of patients with advanced, LKB-1 inactive lung adenocarcinoma. Enrolled patients will be randomized in a 1:1 ratio to receive cisplatin/carboplatin and pemetrexed with the addition of metformin alone (Arm A) or metformin plus FMD (Arm B). The FAME study will use a "pick-the-winner" design with the aim of establishing which of the 2 experimental treatments is superior in terms of antitumor efficacy and safety. The primary assumption of the study is that the combination of the 2 experimental treatments shall improve median progression-free survival from 7.6 months (historical data with chemotherapy alone) to 12 months. Secondary study endpoints are: objective response rate, overall survival, treatment tolerability, and compliance to the experimental treatment.

Identifiants

pubmed: 30617039
pii: S1525-7304(18)30335-8
doi: 10.1016/j.cllc.2018.12.011
pii:
doi:

Substances chimiques

Platinum Compounds 0
Pemetrexed 04Q9AIZ7NO
Metformin 9100L32L2N
Protein Serine-Threonine Kinases EC 2.7.11.1
STK11 protein, human EC 2.7.11.1
AMP-Activated Protein Kinase Kinases EC 2.7.11.3

Types de publication

Clinical Trial Protocol Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e413-e417

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Claudio Vernieri (C)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy. Electronic address: claudio.vernieri@istitutotumori.mi.it.

Diego Signorelli (D)

Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Giulia Galli (G)

Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Monica Ganzinelli (M)

Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Massimo Moro (M)

Tumor Genomics Unit, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandra Fabbri (A)

Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Elena Tamborini (E)

Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Mirko Marabese (M)

Laboratory of Molecular Pharmacology, Department of Oncology, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Milan, Italy.

Elisa Caiola (E)

Laboratory of Molecular Pharmacology, Department of Oncology, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Milan, Italy.

Massimo Broggini (M)

Laboratory of Molecular Pharmacology, Department of Oncology, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Milan, Italy.

Lital Hollander (L)

Laboratory of Methodology for Biomedical Research, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Milan, Italy.

Rosaria Gallucci (R)

Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Giulia Vandoni (G)

Unit of Nutrition Therapy, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Cecilia Gavazzi (C)

Unit of Nutrition Therapy, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Tiziana Triulzi (T)

Molecular Targeting Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Mario Paolo Colombo (MP)

Department of Experimental Oncology and Molecular Medicine, Molecular Immunology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Angela Maria Rizzo (AM)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.

Paola Antonia Corsetto (PA)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.

Giancarlo Pruneri (G)

Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; School of Medicine, University of Milan, Milan, Italy.

Filippo de Braud (F)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; Oncology and Haemato-Oncology Department, University of Milan, Milan, Italy.

Gabriella Sozzi (G)

Tumor Genomics Unit, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Valter Torri (V)

Laboratory of Methodology for Biomedical Research, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Milan, Italy.

Marina Chiara Garassino (MC)

Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. Electronic address: marina.garassino@istitutotumori.mi.it.

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Classifications MeSH