Exploiting FAsting-mimicking Diet and MEtformin to Improve the Efficacy of Platinum-pemetrexed Chemotherapy in Advanced LKB1-inactivated Lung Adenocarcinoma: The FAME Trial.
AMP-Activated Protein Kinase Kinases
Adenocarcinoma of Lung
/ genetics
Adolescent
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Diet Therapy
Fasting
Female
Humans
Lung Neoplasms
/ genetics
Male
Metformin
/ administration & dosage
Middle Aged
Mutation
/ genetics
Neoplasm Staging
Pemetrexed
/ therapeutic use
Platinum Compounds
/ therapeutic use
Protein Serine-Threonine Kinases
/ genetics
Survival Analysis
Young Adult
Cancer metabolism
LKB1 inactivation
Overall survival
Progression-free survival
Safety
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
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-e417Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.