Frailty and adverse clinical outcomes in prostate cancer patients: An analysis from the RADICAL-PC cohort.

R Rocio Consuelo Baro Vila (ICBA, Buenos Aires, Argentina) J Jehonathan H. Pinthus S Sarah Karampatos (McMaster University, Hamilton, ON, Canada) C Cristina Cano Garcia R Rajibul Mian (Population Health Research Institute, McMaster University, Hamilton, ON, Canada) J Jose Lopez-Lopez (Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, ON, Canada) A Ariel Galapo Kann (Clinical Oncology, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil) P Philippe Violette (Woodstock General Hospital, Woodstock, ON, Canada) S surya Prakash V (Yashoda Hospital, Hyderabad, India) V Vincent Fradet P Patrick Anderson N Nicolas Villareal Trujillo (FOSCAL, Bogota, Colombia) L Li Ling Tan (National University Heart Centre, Singapore, Singapore) R Robert Sabbagh L Luke Lavallee (Department of Urology, University of Ottawa, Ottawa, ON, Canada) L Lívia Oliveira (Centro De Pesquisa Clínica Do HC/UFTM/EBSERH, Uberaba, Brazil) D Darryl Leong (Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, ON, Canada)

Abstract

80 Background: As a disease of older individuals, prostate cancer (PC) may feature physical frailty. Most related studies are retrospective and focus on short-term surgical outcomes. Methods: We conductedan analysis of a prospective study of PC patients either diagnosed within the past year, treated with androgen deprivation therapy (ADT) for the first time within the past six months, or scheduled to initiate ADT within a month . Frailty was assessed using Fried's criteria which includes five domains [Handgrip strength, gait speed, physical activity, unintentional weight loss (>4 kg/year) and exhaustion (≥3 days/week)]. Patients were classified as frail (≥3 criteria), pre-frail (1-2 criteria), or robust (0 criteria). Participants were followed annually to ascertain the occurrence of mortality, new metastases, major adverse cardiovascular events (MACE: myocardial infarction, stroke, cardiovascular death, stroke, heart failure, peripheral arterial disease, venous thromboembolism or arterial revascularization) and hospitalization. The relationship between frailty and these events was evaluated by Cox proportional hazards models adjusted for age at enrolment, education, race, tobacco and alcohol use, diabetes, past history of cardiovascular disease, estimated glomerular filtration rate, PC risk, metastatic disease and ADT exposure. Results: We studied 4304 participants (mean age 69±8 years) from 9 countries: 1429 (33%) were robust, 2394 (56%) pre-frail and 481 (11%), frail. During a median 2.4 years, 336 (8%) died, 161 (4%) died from PC or developed new metastases, 506 (12%) were hospitalized and 262 (6%) experienced MACE. Being prefrail or frail was associated with a higher risk of death, hospitalization and MACE but not PC death or new metastases (Table). Conclusions: Pre-frailty and frailty are common among patients with PC. Frailty is associated with approximately a two-fold increase in mortality, hospitalization or MACE in PC patients independent of a wide range of prognostic factors. Relationship between frailty and clinical outcomes. Characteristic Death Hospitalization PC death or new metastases MACE Hazard ratio (95% confidence interval) p-value Hazard ratio (95% confidence interval) p-value Hazard ratio (95% confidence interval) p-value Hazard ratio (95% confidence interval) p-value Frailty Robust Pre-frail Frail Ref1.54(1.13-2.00)2.90(2.00-4.21) 0.007<0.001 Ref1.39(1.10-1.74)2.29(1.70-3.09) 0.005<0.001 Ref1.05(0.70-1.57)1.47(0.85-2.52) 0.830.17 Ref1.44(1.05-1.97)2.21(1.46-3.34) 0.023<0.001 Estimates are from Cox proportional hazards models adjusted for age at enrolment, education, race, tobacco and alcohol use, diabetes, past history of cardiovascular disease, estimated glomerular filtration rate, PC risk, metastatic disease and ADT exposure.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 80-80
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

R

Rocio Consuelo Baro Vila

ICBA, Buenos Aires, Argentina

J

Jehonathan H. Pinthus

S

Sarah Karampatos

McMaster University, Hamilton, ON, Canada

C

Cristina Cano Garcia

R

Rajibul Mian

Population Health Research Institute, McMaster University, Hamilton, ON, Canada

J

Jose Lopez-Lopez

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, ON, Canada

A

Ariel Galapo Kann

Clinical Oncology, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil

P

Philippe Violette

Woodstock General Hospital, Woodstock, ON, Canada

S

surya Prakash V

Yashoda Hospital, Hyderabad, India

V

Vincent Fradet

P

Patrick Anderson

N

Nicolas Villareal Trujillo

FOSCAL, Bogota, Colombia

L

Li Ling Tan

National University Heart Centre, Singapore, Singapore

R

Robert Sabbagh

L

Luke Lavallee

Department of Urology, University of Ottawa, Ottawa, ON, Canada

L

Lívia Oliveira

Centro De Pesquisa Clínica Do HC/UFTM/EBSERH, Uberaba, Brazil

D

Darryl Leong

Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, ON, Canada