Personalized frailty risk assessment in long-term survivors of colorectal cancer.

R Rebecca Forman (Yale New Haven Hospital, New Haven, CT) S Sarah Westvold (Yale Cancer Outcomes, Public Policy and Effectiveness Research Center, New Haven, CT) J Jessica B. Long (Yale Cancer Outcomes, Public Policy and Effectiveness Research Center, Yale School of Medicine, New Haven, CT) J Jane Fan (Yale University, New Haven, CT) T Terry Hyslop (Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA) F Faiza Yasin (Dana-Farber Cancer Institute, Boston, MA) K Kerry Conlin (Yale School of Public Health, New Haven, CT) S Sofia I Jacobson (Yale College, New Haven, CT) A Andrea Silber S Shi-Yi Wang M Michael Leapman (Department of Urology, Yale School of Medicine, New Haven, CT) I Ira L Leeds (Yale School of Medicine, Department of Surgery, Division of Colon and Rectal Surgery, New Haven, CT) M Michael Cecchini (Yale University School of Medicine, New Haven, CT) L Lisa P. Spees S Stephanie B. Wheeler C Cary Philip Gross (National Clinician Scholars Program; Yale Cancer Outcomes, Public Policy and Effectiveness Research Center; Yale School of Medicine, New Haven, CT) K Kevin C. Oeffinger (DCI Center for Onco‐Primary Care Duke University Durham North Carolina USA) M Michaela Ann Dinan (Yale School of Public Health, New Haven, CT)

Abstract

65 Background: Frailty, a pathologic form of aging, is associated with reduced quality of life and increased risk of death. Its incidence increases with age. Frailty is a concern for cancer survivors, especially since this population is surviving longer and increasing in size. There is a need to predict which patients are at risk of frailty to tailor preventative measures, particularly in early-stage colon and rectal cancer survivors, the largest group in gastrointestinal cancer survivors. Methods: This was a retrospective cohort study of individuals aged 66 and older in the SEER-Medicare linked database, diagnosed with stage I-III colon or rectal cancer between 2003-2012. Patients included in the study received definitive surgical treatment and survived for at least 5 years after diagnosis. Frailty was assessed using administrative claims codes with the Kim frailty index. Patients already frail at year 5 were excluded from the analysis. An increase in frailty score, indicating the onset of frailty or worsening to moderate or severe frailty, occurring within 5-10 years following cancer diagnosis was the primary outcome. Predictors of frailty were identified using restricted mean survival time (RMST) regression, with results less than 1 indicating a shorter time to frailty, and significant factors were used to develop a clinical prediction model and stratify patients into risk tertiles. Results: At 10 years or end of available follow-up, 58% of the patients had developed new onset or worsening frailty. There were no significant differences in RMST by patient race, sex, cancer stage and grade. Receipt of systemic therapy 4-5 years after diagnosis, having an ostomy present in years 4-5, advancing age, comorbidities, and living in an area with a greater proportion of residents below the federal poverty line were all associated with shorter time to frailty; the largest effects were seen with advancing age and comorbidities (Table). Our clinical prediction model incorporated age>85 and having multiple comorbidities for both cohorts and ostomy in years 4-5 for the colon cohort. Conclusions: Our population level analysis provided a clinical prediction model for frailty 5-10 years after cancer diagnosis in colon and rectal cancer survivors and may help inform long-term survivorship management. RMST for selected variables. Selected Variables RMST for Colon Cohort (95% CI) RMST for Rectal Cohort (95% CI) Age 85-89 (ref: age 71-74) 0.76 (0.73, 0.79) 0.79 (0.74, 0.84) Age 90+ (ref: age 71-74) 0.67 (0.64, 0.70) 0.74 (0.66, 0.82) 20-100% area-level poverty (ref: 0-<5%) 0.95 (0.92, 0.98) 0.96 (0.91, 1.02) Receiving systemic therapy in years 4-5 0.89 (0.85, 0.92) Not selected Ostomy in years 4-5 0.80 (0.69, 0.92) 0.97 (0.92, 1.02) Elixhauser Comorbidity Index (ECI) 1-2 (reference: ECI 0) 0.77 (0.75, 0.79) 0.79 (0.76, 0.82) ECI 3 (ref: ECI 0) 0.60 (0.57, 0.64) 0.67 (0.59, 0.76)

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 65-65
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

R

Rebecca Forman

Yale New Haven Hospital, New Haven, CT

S

Sarah Westvold

Yale Cancer Outcomes, Public Policy and Effectiveness Research Center, New Haven, CT

J

Jessica B. Long

Yale Cancer Outcomes, Public Policy and Effectiveness Research Center, Yale School of Medicine, New Haven, CT

J

Jane Fan

Yale University, New Haven, CT

T

Terry Hyslop

Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA

F

Faiza Yasin

Dana-Farber Cancer Institute, Boston, MA

K

Kerry Conlin

Yale School of Public Health, New Haven, CT

S

Sofia I Jacobson

Yale College, New Haven, CT

A

Andrea Silber

S

Shi-Yi Wang

M

Michael Leapman

Department of Urology, Yale School of Medicine, New Haven, CT

I

Ira L Leeds

Yale School of Medicine, Department of Surgery, Division of Colon and Rectal Surgery, New Haven, CT

M

Michael Cecchini

Yale University School of Medicine, New Haven, CT

L

Lisa P. Spees

S

Stephanie B. Wheeler

C

Cary Philip Gross

National Clinician Scholars Program; Yale Cancer Outcomes, Public Policy and Effectiveness Research Center; Yale School of Medicine, New Haven, CT

K

Kevin C. Oeffinger

DCI Center for Onco‐Primary Care Duke University Durham North Carolina USA

M

Michaela Ann Dinan

Yale School of Public Health, New Haven, CT