Survival differences in metropolitan versus nonmetropolitan/rural counties in the US: An analysis according to rural-urban continuum codes (RUCC) in the lymphoma epidemiology of outcomes (LEO) study cohort

M Mario Ballerini (1Department of Hematology, UCO Ematologia Azienda Sanitaria Giuliano Isontina (ASUGI), Trieste, Italy) M Melissa Larson (2Mayo Clinic, Rochester, United States) J James Foran (6Mayo Clinic Comprehensive Cancer Center, Jacksonville, United States) M Matthew Bryant Howren (4Department of Internal Medicine, University of Iowa, Iowa City, United States) M Michelle Hildebrandt (UT MD Anderson Cancer Center, Houston, Texas, United States) P Pamela Allen S Shaun Riska (2Department of Quantitative Health Sciences, Mayo Clinic, Rochester, United States) M Matthew Maurer (2Mayo Clinic, Rochester, United States) S Susan Slager A Andrew Feldman (2Mayo Clinic, Rochester, United States) D David Jaye (8Emory, Atlanta, United States) T Thomas Habermann (2Mayo Clinic, Rochester, United States) J Jonathon Cohen (15Winship Cancer Institute, Emory University, Atlanta CA) B Brad Kahl (8Washington University, Division of Oncology, St. Louis, United States) P Peter Martin I Izidore S. Lossos (29Division of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL) J Jonathan Friedberg (15Wilmot Cancer Center, University of Rochester, Department of Medicine, Hematology/Oncology, Rochester, United States) B Brian Link (13University of Iowa, Iowa City, United States) E Eric Mou (24Division of Hematology, Oncology, and Blood and Marrow Transplantation, Department of Internal Medicine, University of Iowa, Iowa City, IA) C Chijioke Nze (6MD Anderson Cancer Center, Houston, United States) C Carrie Thompson (1Mayo Clinic College of Medicine, Rochester, MN) A Annalynn Williams (13Wilmot Cancer Institute, University of Rochester, Rochester, United States) K Kathleen Yost (2Department of Quantitative Health Sciences, Mayo Clinic, Rochester, United States) C Christopher Flowers (1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX) J James Cerhan (2Mayo Clinic, Rochester, United States)

Abstract

Abstract Background: Rural/nonmetropolitan (nonmetro) counties face known barriers to comprehensive cancer care compared with metropolitan (metro) counties, which may impact the outcomes for lymphoma patients. We evaluated the impact metro vs nonmetro status on outcomes after a diagnosis of non-Hodgkin lymphoma (NHL) in the context of clinical, demographic, and lifestyle factors. Methods: Of 7724 participants enrolled in the prospective LEO cohort study from 2015-2020, 7610 (98.5%) had their county of residence at diagnosis assigned a RUCC (2013) code. We compared outcomes of participants from metro (defined as RUCC 1-3, which are central counties with ≥1 urban areas of ≥50,000) vs nonmetro counties (RUCC 4-9, which are counties with smaller urban areas as well as completely rural). We estimated hazard ratios (HRs) and 95% confidence intervals (CI) from univariable and multivariable Cox models for associations of metro status with overall survival (OS). Cause of death (lymphoma [including treatment related], non-lymphoma, unknown) was assessed using a competing risk approach. Results: Compared with metro counties (N=6096), LEO participants from nonmetro counties (N=1514) were older (median age 64 vs 62 years; p<0.001), more likely to be non-Hispanic white (94% vs 75%; p<0.001) and married (84% vs 75%; p<0.001), and less likely to have completed graduate or professional school education (16% vs 27%; p<0.001). There were no notable differences (>5%) by metro status for sex, employment status, NHL subtype, stage, performance status, abnormal lactate dehydrogenase (LDH), international prognostic index (IPI), number of comorbidities, time from diagnosis to treatment interval (DTI) or participation in a clinical trial. Compared with LEO participants from metro counties, those from nonmetro counties had inferior OS at 5 years (74.5% vs 78.4%; HR=1.23, CI 1.10-1.37; p<0.001). The OS association only slightly attenuated after adjustment for age, sex, race/ethnicity and NHL subtype (HR=1.20, CI 1.07-1.34; p=0.002), and held in models that adjusted for clinical prognostic factors (stage, NHL subtype, IPI, DTI), socioeconomic status (SES; education, marital status), health status (comorbidity, frailty), or lifestyle factors (smoking, body mass index). Using a competing risk model, the cumulative incidence of death at 5 years due to lymphoma (16.9% vs 14.1%; p=0.002) and non-lymphoma (5.9% vs 3.9%; p=0.002) was higher for participants from nonmetro vs metro counties, respectively. For participants <65 years, nonmetro vs metro status had inferior OS (HR=1.40, CI 1.17-1.67; p<0.001). This association remained after adjustment for age, sex, race/ethnicity and NHL subtype (HR=1.36, CI 1.14-1.63; p<0.001), as well as after adjustment for clinical prognostic, SES, health status, or lifestyle factors. The cumulative incidence of death at 5 years due to lymphoma was higher in participants from nonmetro vs metro counties (15.1% vs 11.5%; p=0.002), while there was no difference by metro status for non-lymphoma related deaths (2.1% vs 1.7%; p=0.47). In contrast, for participants age 65+ years, there was no differences by metro status for OS (HR=1.04, CI 0.91-1.20; p=0.56). After adjustment for age, sex, race/ethnicity and NHL subtype, participants from nonmetro areas had inferior OS (HR=1.12, 0.97-1.29) although this was not statistically significant (p=0.13), and was attenuated in models adjusting for clinical, health status, or lifestyle factors. The cumulative incidence of death at 5 years due to lymphoma was no different in participants from nonmetro vs metro counties (18.9% vs 18.0%; p=0.37), while non-lymphoma related deaths were higher in nonmetro counties (9.9% vs 6.8%; p=0.017). Conclusion: LEO participants from nonmetro vs metro counties had inferior OS overall, although this was predominately observed for younger (<65 years) participants. These associations did not appear to be explained by demographic, NHL subtype, clinical, SES, health status, or lifestyle factors. Of particular note, the risk of death due to lymphoma was higher in nonmetro areas for participants <65 years but not those 65+ years, while the risk of death due to other causes was higher in nonmetro areas for participants 65+ years but not those <65 years. These findings require further study, particularly related to barriers to care, and suggest the potential need for age-specific strategies to optimize outcomes for NHL patients from nonmetro/rural areas.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 6324-6324
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (25)

M

Mario Ballerini

1Department of Hematology, UCO Ematologia Azienda Sanitaria Giuliano Isontina (ASUGI), Trieste, Italy

M

Melissa Larson

2Mayo Clinic, Rochester, United States

J

James Foran

6Mayo Clinic Comprehensive Cancer Center, Jacksonville, United States

M

Matthew Bryant Howren

4Department of Internal Medicine, University of Iowa, Iowa City, United States

M

Michelle Hildebrandt

UT MD Anderson Cancer Center, Houston, Texas, United States

P

Pamela Allen

S

Shaun Riska

2Department of Quantitative Health Sciences, Mayo Clinic, Rochester, United States

M

Matthew Maurer

2Mayo Clinic, Rochester, United States

S

Susan Slager

A

Andrew Feldman

2Mayo Clinic, Rochester, United States

D

David Jaye

8Emory, Atlanta, United States

T

Thomas Habermann

2Mayo Clinic, Rochester, United States

J

Jonathon Cohen

15Winship Cancer Institute, Emory University, Atlanta CA

B

Brad Kahl

8Washington University, Division of Oncology, St. Louis, United States

P

Peter Martin

I

Izidore S. Lossos

29Division of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL

J

Jonathan Friedberg

15Wilmot Cancer Center, University of Rochester, Department of Medicine, Hematology/Oncology, Rochester, United States

B

Brian Link

13University of Iowa, Iowa City, United States

E

Eric Mou

24Division of Hematology, Oncology, and Blood and Marrow Transplantation, Department of Internal Medicine, University of Iowa, Iowa City, IA

C

Chijioke Nze

6MD Anderson Cancer Center, Houston, United States

C

Carrie Thompson

1Mayo Clinic College of Medicine, Rochester, MN

A

Annalynn Williams

13Wilmot Cancer Institute, University of Rochester, Rochester, United States

K

Kathleen Yost

2Department of Quantitative Health Sciences, Mayo Clinic, Rochester, United States

C

Christopher Flowers

1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

J

James Cerhan

2Mayo Clinic, Rochester, United States