Racial Disparity in Pathologic Response following Neoadjuvant Chemotherapy in Resected Pancreatic Cancer: A Multi-Institutional Analysis from the Central Pancreatic Consortium.


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:
Mar 2023
Historique:
received: 10 06 2022
accepted: 10 10 2022
pubmed: 2 11 2022
medline: 11 2 2023
entrez: 1 11 2022
Statut: ppublish

Résumé

Major pathologic response (MPR) following neoadjuvant therapy (NAT) in pancreatic ductal adenocarcinoma (PDAC) patients undergoing resection is associated with improved survival. We sought to determine whether racial disparities exist in MPR rates following NAT in patients with PDAC undergoing resection. Patients with potentially operable PDAC receiving at least 2 cycles of neoadjuvant FOLFIRINOX or gemcitabine/nab-paclitaxel ± radiation followed by pancreatectomy (2010-2019) at 7 high-volume centers were reviewed. Self-reported race was dichotomized as Black and non-Black, and multivariable models evaluated the association between race and MPR (i.e., pathologic complete response [pCR] or near-pCR). Cox regression evaluated the association between race and disease-free (DFS) and overall survival (OS). Results of 486 patients who underwent resection following NAT (mFOLFIRINOX 56%, gemcitabine/nab-paclitaxel 25%, radiation 29%), 67 (13.8%) patients were Black. Black patients had lower CA19-9 at diagnosis (median 67 vs. 204 U/mL; P = 0.003) and were more likely to undergo mild/moderate chemotherapy dose modification (40 vs. 20%; P = 0.005) versus non-Black patients. Black patients had significantly lower rates of MPR compared with non-Black patients (13.4 vs. 25.8%; P = 0.039). Black race was independently associated with worse MPR (OR 0.26, 95% confidence interval [CI] 0.10-0.69) while controlling for NAT duration, CA19-9 dynamics, and chemotherapy modifications. There was no significant difference in DFS or OS between Black and non-Black cohorts. Black patients undergoing pancreatectomy appear less likely to experience MPR following NAT. The contribution of biologic and nonbiologic factors to reduced chemosensitivity in Black patients warrants further investigation.

Sections du résumé

BACKGROUND BACKGROUND
Major pathologic response (MPR) following neoadjuvant therapy (NAT) in pancreatic ductal adenocarcinoma (PDAC) patients undergoing resection is associated with improved survival. We sought to determine whether racial disparities exist in MPR rates following NAT in patients with PDAC undergoing resection.
METHODS METHODS
Patients with potentially operable PDAC receiving at least 2 cycles of neoadjuvant FOLFIRINOX or gemcitabine/nab-paclitaxel ± radiation followed by pancreatectomy (2010-2019) at 7 high-volume centers were reviewed. Self-reported race was dichotomized as Black and non-Black, and multivariable models evaluated the association between race and MPR (i.e., pathologic complete response [pCR] or near-pCR). Cox regression evaluated the association between race and disease-free (DFS) and overall survival (OS).
RESULTS RESULTS
Results of 486 patients who underwent resection following NAT (mFOLFIRINOX 56%, gemcitabine/nab-paclitaxel 25%, radiation 29%), 67 (13.8%) patients were Black. Black patients had lower CA19-9 at diagnosis (median 67 vs. 204 U/mL; P = 0.003) and were more likely to undergo mild/moderate chemotherapy dose modification (40 vs. 20%; P = 0.005) versus non-Black patients. Black patients had significantly lower rates of MPR compared with non-Black patients (13.4 vs. 25.8%; P = 0.039). Black race was independently associated with worse MPR (OR 0.26, 95% confidence interval [CI] 0.10-0.69) while controlling for NAT duration, CA19-9 dynamics, and chemotherapy modifications. There was no significant difference in DFS or OS between Black and non-Black cohorts.
CONCLUSIONS CONCLUSIONS
Black patients undergoing pancreatectomy appear less likely to experience MPR following NAT. The contribution of biologic and nonbiologic factors to reduced chemosensitivity in Black patients warrants further investigation.

Identifiants

pubmed: 36316508
doi: 10.1245/s10434-022-12741-4
pii: 10.1245/s10434-022-12741-4
doi:

Substances chimiques

CA-19-9 Antigen 0
Pancreatic Hormones 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1485-1494

Subventions

Organisme : National Cancer Institute (NCI)
ID : Nipun B. Merchant T32CA211034
Organisme : National Institutes of Health (NIH)
ID : Jashodeep Datta UL1TR002736

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. Society of Surgical Oncology.

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Auteurs

Ifeanyichukwu Ogobuiro (I)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA.

Amber L Collier (AL)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA.

Khadeja Khan (K)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA.

Iago de Castro Silva (I)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA.

Deukwoo Kwon (D)

Department of Surgery, Icahn School of Medicine at Mount Sinai Department of Population Health Science and Policy, New York, NY, USA.

Gregory C Wilson (GC)

Department of Surgery, University of Cincinnati School of Medicine, Cincinnati, OH, USA.

Patrick B Schwartz (PB)

Department of Surgery, Carbone Cancer Center, University of Wisconsin School of Medicine, Madison, WI, USA.

Alexander A Parikh (AA)

Department of Surgery, East Carolina University Brody School of Medicine, Greenville, NC, USA.

Chet Hammill (C)

Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Hong J Kim (HJ)

Department of Surgery, Lineberger Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

David A Kooby (DA)

Department of Surgery, Emory University School of Medicine, Winship Cancer Institute, Atlanta, GA, USA.

Daniel Abbott (D)

Department of Surgery, Carbone Cancer Center, University of Wisconsin School of Medicine, Madison, WI, USA.

Shishir K Maithel (SK)

Department of Surgery, Emory University School of Medicine, Winship Cancer Institute, Atlanta, GA, USA.

Rebecca A Snyder (RA)

Department of Surgery, East Carolina University Brody School of Medicine, Greenville, NC, USA.

Syed A Ahmad (SA)

Department of Surgery, University of Cincinnati School of Medicine, Cincinnati, OH, USA.

Nipun B Merchant (NB)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA.

Jashodeep Datta (J)

Department of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1120 NW 14th Street, Suite 410, Miami, FL, 33136, USA. jash.datta@med.miami.edu.

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