Skip to main content

ORIGINAL RESEARCH article

Front. Aging
Sec. Aging, Metabolism and Redox Biology
Volume 5 - 2024 | doi: 10.3389/fragi.2024.1268232

The FITNESS Study: Longitudinal Geriatric Assessment, Treatment Toxicity, and Biospecimen Collection to Assess Functional Disability Among Older Adults with Lung Cancer Provisionally Accepted

 Madison Grogan1 Rebecca Hoyd1  Jason Benedict2 Sarah Janse2 Nyelia Williams1 Michelle Naughton3 Christin E. Burd4, 5  Electra D. Paskett3  Ashley Rosko1  Dan Spakowicz1, 3, 4  Carolyn Presley1*
  • 1Division of Medical Oncology, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, United States
  • 2Center for Biostatistics, College of Medicine, The Ohio State University, United States
  • 3Division of Cancer Prevention and Control, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, United States
  • 4Pelotonia Institute for Immuno-Oncology, Comprehensive Cancer Center, The Ohio State University, United States
  • 5Department of Cancer Biology and Genetics, College of Medicine, The Ohio State University, United States

The final, formatted version of the article will be published soon.

Receive an email when it is updated
You just subscribed to receive the final version of the article

Introduction: Older adults with chronic disease prioritize functional independence. We aimed to describe the feasibility of capturing functional disability and treatment toxicity among older adults with lung cancer using a longitudinal comprehensive geriatric assessment (CGA) and molecular biomarkers of aging.

Methods: This prospective study included adults ≥60 years with any newly diagnosed non-small-cell lung cancer. Participants were recruited from central Ohio (2018-2020). Study assessments included the Cancer and Aging Research Group CGA (CARG-CGA), short physical performance battery (SPPB), and the blessed orientation-memory concentration (BOMC) test at baseline, 3, 6, and 12 months. Activities of daily living (ADLs) and instrumental ADLs (IADLs), quality of life (QoL, PROMIS 10), and treatment toxicity were captured monthly. Stool and blood were collected to characterize the gut microbiome and age-related blood biomarkers.

Results: This study enrolled 50 participants with an average age of 71.7 years. Ninety-two percent of participants were Caucasian, 58% were male, and all were non-Hispanic. Most had advanced stage (stage III/IV: 90%; stage I/II: 10%), with adenocarcinoma the predominant histologic subtype (68% vs. 24% squamous). First-line treatments included chemotherapy (44%), immune checkpoint inhibitors (ICIs, 22%), chemotherapy and ICIs (30%), or tyrosine kinase inhibitors (4%). The median baseline CARG toxicity score was 8 (range 2-12). Among patients with treatment-related toxicity (n=49), 39 (79.6%) cases were mild (grade 1-2), and 10 (20.4%) were moderate to severe (≥ grade 3). Treatment toxicity was greater among those with a CARG score ≥8 (28.0% vs. 13.6%). Higher IADL independence, QoL, and SPPB scores at baseline were positively associated with Candidatus Gastranaerophilales bacterium, Lactobacillus rogosae, and Enterobacteria phage P4. Romboutsia ilealis, Streptococcus, and Lachnoclostridium sp An138 and T cell lag3 and cd8a were associated with worse IADLs, QoL, and SPPB scores at baseline.

Discussion: A longitudinal CGA and biomarker collection is feasible among older adults undergoing lung cancer treatment. Gut microbe and T cell gene expression changes correlated with subjective and objective functional status assessments. Future research will test causality in these associations to improve outcomes through novel supportive care interventions to prevent functional disability.

Keywords: lung cancer, functional decline, Aging, biomarkers, microbiome, novel treatments

Received: 27 Jul 2023; Accepted: 06 May 2024.

Copyright: © 2024 Grogan, Hoyd, Benedict, Janse, Williams, Naughton, Burd, Paskett, Rosko, Spakowicz and Presley. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Dr. Carolyn Presley, Division of Medical Oncology, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, Columbus, 43210, Ohio, United States