Racial/Ethnic Disparities in the Era of Minimally Invasive Surgery for Treatment of Colorectal Cancer.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 01 02 2023
accepted: 17 05 2023
medline: 20 9 2023
pubmed: 10 7 2023
entrez: 9 7 2023
Statut: ppublish

Résumé

Minimally invasive (laparoscopic and robotic) surgery (MIS) for colorectal cancer is associated with improved outcomes. We sought to characterize possible disparities in surgical approach and outcomes. In this cross-sectional study, colorectal adenocarcinoma cases among non-Hispanic white (NHW), non-Hispanic Black (NHB), and Hispanic patients were identified using the National Cancer Database (2010-2017). Logistic and Poisson regressions, generalized logit models, and Cox proportional hazards were used to assess outcomes, with reclassification of surgery type if converted to open. NHB patients were less likely to undergo robotic surgery. After multivariable analysis, NHB patients were 6% less likely, while Hispanic patients were 12% more likely to undergo a MIS approach. Lymph node retrieval was higher (> 1.3% more, p < 0.0001) and length of stay was shorter (> 17% shorter, p < 0.0001) for MIS approaches. Unplanned readmission was lower for MIS colon cancer operations compared with open operations, but not for rectal cancer. Race/ethnicity-adjusted risk of death was lower with MIS approaches for colon as well as rectal cancer. After adjusting for surgery type, risk of death was 12% lower for NHB and 35% lower for Hispanic patients compared with NHW patients. Hispanic patients had 21% lower risk of death, while NHB patients had 12% higher risk of death than NHW patients with rectal cancer, after adjusting for surgery type. Racial/ethnic disparities exist in utilization of MIS for colorectal cancer treatment, disproportionately affecting NHB patients. Since MIS has the potential to improve outcomes, suboptimal access may contribute to harmful and thus unacceptable disparities in survivorship.

Sections du résumé

BACKGROUND BACKGROUND
Minimally invasive (laparoscopic and robotic) surgery (MIS) for colorectal cancer is associated with improved outcomes. We sought to characterize possible disparities in surgical approach and outcomes.
PATIENTS AND METHODS METHODS
In this cross-sectional study, colorectal adenocarcinoma cases among non-Hispanic white (NHW), non-Hispanic Black (NHB), and Hispanic patients were identified using the National Cancer Database (2010-2017). Logistic and Poisson regressions, generalized logit models, and Cox proportional hazards were used to assess outcomes, with reclassification of surgery type if converted to open.
RESULTS RESULTS
NHB patients were less likely to undergo robotic surgery. After multivariable analysis, NHB patients were 6% less likely, while Hispanic patients were 12% more likely to undergo a MIS approach. Lymph node retrieval was higher (> 1.3% more, p < 0.0001) and length of stay was shorter (> 17% shorter, p < 0.0001) for MIS approaches. Unplanned readmission was lower for MIS colon cancer operations compared with open operations, but not for rectal cancer. Race/ethnicity-adjusted risk of death was lower with MIS approaches for colon as well as rectal cancer. After adjusting for surgery type, risk of death was 12% lower for NHB and 35% lower for Hispanic patients compared with NHW patients. Hispanic patients had 21% lower risk of death, while NHB patients had 12% higher risk of death than NHW patients with rectal cancer, after adjusting for surgery type.
CONCLUSIONS CONCLUSIONS
Racial/ethnic disparities exist in utilization of MIS for colorectal cancer treatment, disproportionately affecting NHB patients. Since MIS has the potential to improve outcomes, suboptimal access may contribute to harmful and thus unacceptable disparities in survivorship.

Identifiants

pubmed: 37423924
doi: 10.1245/s10434-023-13693-z
pii: 10.1245/s10434-023-13693-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6748-6759

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016059
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA242003
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA233444
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA233444-03S1
Pays : United States
Organisme : NHGRI NIH HHS
ID : T32 HG008958
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016059
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA242003
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA233444
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA233444-03S1
Pays : United States
Organisme : NHGRI NIH HHS
ID : T32 HG008958
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023. Society of Surgical Oncology.

Références

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Auteurs

Andrea N Riner (AN)

Department of Surgery, University of Florida College of Medicine, Gainesville, FL, USA.

Kelly M Herremans (KM)

Department of Surgery, University of Florida College of Medicine, Gainesville, FL, USA.

Xiaoyan Deng (X)

Department of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.

Dipankar Bandyopadhyay (D)

Department of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.

Steven D Wexner (SD)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Jose G Trevino (JG)

Department of Surgery, Virginia Commonwealth University, Richmond, VA, USA.
Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.

Stephen P Sharp (SP)

Department of Surgery, Virginia Commonwealth University, Richmond, VA, USA. Stephen.Sharp@vcuhealth.org.

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