Resiliency among older adults receiving lung cancer treatment (ROAR-LCT): A novel supportive care intervention for older adults with advanced lung cancer.

Functional resiliency Functional status Lung cancer Older adults Physical therapy Progressive muscle relaxation Supportive care intervention

Journal

Journal of geriatric oncology
ISSN: 1879-4076
Titre abrégé: J Geriatr Oncol
Pays: Netherlands
ID NLM: 101534770

Informations de publication

Date de publication:
21 Aug 2024
Historique:
received: 26 04 2024
revised: 28 06 2024
accepted: 31 07 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 22 8 2024
Statut: aheadofprint

Résumé

Novel supportive care interventions designed for an aging population with lung cancer are urgently needed. We aimed to determine the feasibility of a novel supportive care physical therapy (PT) plus progressive muscle relaxation (PMR) intervention delivered to older adults with advanced lung cancer in the United States (US). This clinical trial, Resiliency Among Older Adults Receiving Lung Cancer Treatment (ROAR-LCT: NCT04229381), recruited adults aged ≥60 years with unresectable stage III/IV non-small cell (NSCLC) or small cell lung cancer (SCLC) receiving cancer treatment at The James Thoracic Oncology Center (planned enrollment, N = 20). There were no exclusion criteria pertaining to performance status, laboratory values, prior cancer diagnoses, comorbidities, or brain metastases. Participants were evaluated by PT and psychology and given an exercise pedaler, resistance bands, a relaxation voice recording, and instructions at study initiation. Participants were evaluated in-person by PTs and psychologists at the start and end of the 12-session intervention, with the intervening sessions conducted via virtual health. Participants completed self-reported measures of functional status, symptoms, and mood longitudinally with the following instruments: EQ-5D-5L, Patient Health Questionnaire-9, and General Anxiety Disorder-7. PT assessments included the Short Physical Performance Battery (SPPB) and the two-minute walk test. Feasibility was defined as at least 60% of participants completing at least 70% of all intervention sessions. Optional gut microbiome samples and activity monitoring data (ActiGraph®) were also collected. The ROAR-LCT study concluded after consenting 22 patients. Among the 22 consented, 18 (81.8%) started the intervention; 11 participants (61.1%) completed at least 70% of all study sessions. All participants with SCLC completed the intervention. Reasons for withdrawal included progression of disease or hospitalization. The majority (88.9%) of patients who started were able to complete at least one virtual health session. Participants' functional status, SPPB, depression, and anxiety scores were stable from pre- to post-intervention. Participants who withdrew had worse baseline scores across domains. Seven microbiome and six ActiGraph® samples were collected. This is one of the first PT + PMR supportive care interventions using virtual health among older adults with advanced lung cancer to achieve feasibility in the US.

Identifiants

pubmed: 39174449
pii: S1879-4068(24)00142-5
doi: 10.1016/j.jgo.2024.101844
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101844

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest EP reports grants from Pfizer, Merck Foundation, Genentech, Guardant Health, and AstraZeneca and is on Advisory Boards for GSK and Merck. DC is on the Executive Steering Committee for Lumanity, participated in the Merck Global Lung Expert Input Forum and a Pfizer Egypt Meet the Expert session, and has provided scientific input to Merck. CJP reports grants from the Bristol Myers Squibb Foundation, The Rising Tide Foundation, and is a consultant for Regeneron, RAPT Therapeutics, OncLIVE, and Bristol Myers Squibb.

Auteurs

Carolyn J Presley (CJ)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Madison Grogan (M)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Amy Compston (A)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Karen Hock (K)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Brittany Knauss (B)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Elyse Redder (E)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Nicole A Arrato (NA)

Department of Psychology, The Ohio State University, Columbus, OH, United States.

Stephen B Lo (SB)

Department of Psychology, The Ohio State University, Columbus, OH, United States.

Sarah Janse (S)

Center for Biostatistics, The Ohio State University, Columbus, OH, United States.

Jason Benedict (J)

Center for Biostatistics, The Ohio State University, Columbus, OH, United States.

Rebecca Hoyd (R)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Nyelia Williams (N)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States.

Scott Hayes (S)

Department of Psychology, The Ohio State University, Columbus, OH, United States.

Sharla Wells-Di Gregorio (S)

Division of Palliative Medicine, Department of Internal Medicine, The Ohio State University Columbus, OH, United States.

Thomas M Gill (TM)

Section of Geriatric Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.

Heather Allore (H)

Section of Geriatric Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.

Brian Focht (B)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States; Division of Kinesiology, Department of Human Sciences, The Ohio State University, Columbus, OH, United States.

Morten Quist (M)

University of Copenhagen, Copenhagen, Denmark.

David P Carbone (DP)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States; Pelotonia Institute for Immuno-Oncology, OSUCCC-James, The Ohio State University, Columbus, OH, United States.

Daniel Spakowicz (D)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States; The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States; Pelotonia Institute for Immuno-Oncology, OSUCCC-James, The Ohio State University, Columbus, OH, United States.

Electra D Paskett (ED)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States; Division of Cancer Control and Prevention, Department of Internal Medicine, The Ohio State University, Columbus, OH, United States.

Barbara L Andersen (BL)

The Ohio State University Comprehensive Cancer Center, James Cancer Hospital, & Solove Research Institute, Columbus, OH, United States; Department of Psychology, The Ohio State University, Columbus, OH, United States.

Classifications MeSH