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Pancreatic ductal adenocarcinoma: exploring clinicopathological trends and racial disparities in a comprehensive U.S. population-based study.
Yasinzai, Abdul Qahar Khan; Tareen, Bisma; Tracy, Katharine; Jamil, Nimra; Khan, Marjan; Ullah, Hafeez; Raza, Muhammad; Khan, Amin Ullah; Arif, Dauod; Waheed, Abdul; Sidhwa, Feroze; Misra, Subhasis; Karki, Nabin Raj; Karim, Nagla Abdel; Cavalcante, Ludimila; Ullah, Asad.
Afiliación
  • Yasinzai AQK; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan. abdul.qahar.aqk@gmail.com.
  • Tareen B; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan.
  • Tracy K; Medical College of Georgia, Augusta, GA, 30912, USA.
  • Jamil N; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan.
  • Khan M; Internal Medicine, Marshfield Medical Center, Marshfield, USA.
  • Ullah H; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan.
  • Raza M; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan.
  • Khan AU; Department of Medicine, Bolan Medical College, Quetta, 83700, Pakistan.
  • Arif D; Department of Oncology Developmental Therapeutics, Novant Health, Charlotte, NC, USA.
  • Waheed A; Department of Surgery, San Joaquin General Hospital, French Camp, CA, 95231, USA.
  • Sidhwa F; Department of Surgery, San Joaquin General Hospital, French Camp, CA, 95231, USA.
  • Misra S; Department of Surgery, BayCare Health System, Tampa, FL, USA.
  • Karki NR; Department of Oncology, Mitchell Cancer Institute, University of South Alabama, Mobile, USA.
  • Karim NA; Department of Hematology-Oncology, Inova Schar Cancer Institute, University of Virginia, Fairfax, VA, 22031, USA.
  • Cavalcante L; Department of Oncology Developmental Therapeutics, Novant Health, Charlotte, NC, USA.
  • Ullah A; Department of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX, 79430, USA.
Clin Transl Oncol ; 2024 Apr 14.
Article en En | MEDLINE | ID: mdl-38615292
ABSTRACT

INTRODUCTION:

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy about 50% of PDAC are metastatic at presentation. In this study, we evaluated PDAC demographics, annual trend analysis, racial disparities, survival rate, and the role of different treatment modalities in localized and metastatic disease.

METHODS:

A total of 144,824 cases of PDAC were obtained from the SEER database from 2000 to 2018.

RESULTS:

The median age was 69 years, with a slightly higher incidence in males (52%) and 80% of all cases were white. Among cases with available data, 43% were grade III tumors and 57% were metastatic. The most common site of metastasis was the liver (15.7%). The annual incidence has increased steadily from 2000 to 2018. The overall observed (OS) 5-year survival rate was 4.4% (95% CI 4.3-4.6%), and 5 years cause-specific survival (CSS) was 5% (95% CI 5.1-5.4%). The 5-year survival with multimodal therapy (chemotherapy, surgery, and radiation) was 22% (95% CI 20.5-22.8%). 5-year CSS for the blacks was lower at 4.7% (95% CI 4.2-5.1%) compared to the whites at 5.3% (95% CI 5.1-5.4%). Multivariate analysis found male gender and black race associated with worse prognosis. Kaplan-Meier survival analysis found multimodal therapy to have the best outcomes in all three stages.

CONCLUSION:

PDAC is an aggressive malignancy with male gender and black race are associated with a poor prognosis. Surgery with chemoradiation was associated with the best overall survival. With steadily increasing rates of PDAC, improved treatment modalities are paramount to improving survival in these patients.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Transl Oncol Año: 2024 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Transl Oncol Año: 2024 Tipo del documento: Article País de afiliación: Pakistán