Sa007 RACIAL DISPARITIES AMONG PATIENTS UNDERGOING PANCREATICODUODENECTOMY (WHIPPLE'S PROCEDURE) FOR PANCREATIC ADENOCARCINOMA OR CHOLANGIOCARCINOMA

2021 ◽  
Vol 160 (6) ◽  
pp. S-387
Author(s):  
Ahmed Eltelbany ◽  
Osama Hamid ◽  
Abdul Mohammed ◽  
George Khoudari ◽  
Sushrut Trakroo ◽  
...  
Pancreas ◽  
2016 ◽  
Vol 45 (7) ◽  
pp. e33-e34 ◽  
Author(s):  
Jordan J. Atkins ◽  
Mark A. Fiala ◽  
Andrea Wang-Gillam ◽  
Tanya M. Wildes

2020 ◽  
Author(s):  
Anas M Saad ◽  
Maha AT Elsebaie ◽  
Mohamed Amgad ◽  
Muneer J Al-Husseini ◽  
Kyrillus S Shohdy ◽  
...  

HPB ◽  
2010 ◽  
Vol 12 (5) ◽  
pp. 325-333 ◽  
Author(s):  
Alireza Aslani ◽  
Anthony J. Gill ◽  
Paul J. Roach ◽  
Barry J. Allen ◽  
Ross C. Smith

2019 ◽  
Vol 37 (4_suppl) ◽  
pp. 357-357 ◽  
Author(s):  
Nina Niu Sanford ◽  
Xiaohan Xu ◽  
David J. Sher

357 Background: Adjuvant chemotherapy for resected pancreatic adenocarcinoma is a category 1 NCCN recommendation, however studies have shown that many patients do not go on to receive chemotherapy after definitive surgery. Whether racial disparities exist for receipt of adjuvant chemotherapy is unknown. Methods: The National Cancer Database was used to identify 28,255 patients with non-metastatic pancreatic adenocarcinoma who underwent definitive surgery between 2005-2014. Multivariable logistic regression defined adjusted odds ratio (AOR) and 95% confidence intervals (CI) of receipt of adjuvant chemotherapy by race. Additional variables included in the model were age, sex, stage, node positivity, comorbidity index, facility type and insurance. Among those receiving chemotherapy, multivariable logistic regression assessed odds of treatment with multiagent chemotherapy and among those not receiving chemotherapy, predictors of chemotherapy refusal were assessed. Results: Compared to white patients, black patients were less likely to receive adjuvant chemotherapy (AOR 0.74, 95% CI 0.64-0.85, p < 0.001) and multiagent adjuvant chemotherapy (AOR 0.80, 95% CI 0.72-0.88, p < 0.001). The disparities were limited to patients with comorbidity score of 0 and persisted when analyses were restricted to only academic cancer centers. Among 2,405 patients not treated with chemotherapy, black patients had lower odds of refusing chemotherapy (AOR 0.72, 95% CI 0.55-0.93, p = 0.01). Conclusions: In this nationally representative study, black patients were less likely to receive NCCN-guideline concordant treatment for resected pancreatic adenocarcinoma; this disparity did not appear to be driven by increased refusal of treatment by black patients. Given that differences in quality of care may contribute to disparities in cancer survival, our findings suggest that outcomes for black patients could be improved by increasing the proportion receiving guideline-concordant adjuvant chemotherapy. Further investigation is needed to identify factors leading to the observed differences in this study, such that appropriate interventions can be undertaken to mitigate this disparity.


HPB ◽  
2020 ◽  
Vol 22 (5) ◽  
pp. 735-743
Author(s):  
Alexander M. Fagenson ◽  
Sara M. Grossi ◽  
Kelsey Musgrove ◽  
Naveenraj Solomon ◽  
Pura Rodriguez de la Vega ◽  
...  

2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. A385-A385
Author(s):  
Swetha Murthi ◽  
Paria Zarghamravanbakhsh ◽  
Agustin Busta

Abstract Introduction: Diabetes mellitus and obesity is associated with increased risk of pancreatic cancer which has been postulated to be due to pancreatic beta cell dysfunction and increased insulin resistance. Pancreatic cancer also exerts its effect on pancreatic beta cells, reducing insulin secretion, affecting glucose uptake and increasing insulin resistance. We present a case of pancreatic adenocarcinoma with severe insulin resistance and uncontrolled diabetes which reversed after tumor removal. Clinical Description: 79 year old male patient with no prior diagnosis of diabetes, history of hypertension, atrial fibrillation, cerebrovascular accident got admitted to the hospital with painless jaundice, dark colored urine and pruritus for a month. He also endorsed polyuria, polydipsia and weight loss for 2 months. He underwent Magnetic Resonance Cholangiopancreatography and was diagnosed with a 2.8 cm pancreatic head mass, consistent with adenocarcinoma along with intraductal papillary mucinous neoplasm. He was diagnosed with new onset of diabetes, A1c 12.6% during that hospitalization. He weighed about 75 kg and height 170cm (BMI 26.6). Labs showed normal renal function, deranged liver enzymes with direct hyperbilirubinemia, elevated transaminases and alkaline phosphatase. C-peptide level was 1.2 ng/ml for a blood glucose of 197 mg/dl. He was discharged on once daily insulin Glargine 25 units and mealtime insulin Lispro 10 units three times a day (TID) requiring 0.7 units/kg. During follow-up, his insulin requirement started to increase despite proper insulin injection technique and medication compliance. He required glargine 150 units/day and U500 insulin 50 units TID requiring about 4 units/kg. He underwent Whipple’s procedure, partial pancreas resection after a month of his diagnosis. Patient was started on clear liquid diet and his blood glucose started to get better on post-op day 1 with just correctional insulin. He was discharged on Repaglinide 0.5mg TID with each meal and all his insulin was discontinued. His blood glucose was in range of 80 to 160 mg/dl with Repaglinide during clinical follow-up with regular diabetic diet. His severe insulin resistance got reversed after the resection of pancreatic neoplasm. Conclusion: The pathogenesis of pancreatic cancer associated diabetes has not been studied well. Basic science research found that adrenomedullin, an amionopeptide, is up-regulated in patients with pancreatic cancer and causes insulin resistance in β Cells. Cancer theories also found about metabolic reprogramming and metabolic cross talk happens between pancreatic cancer and peripheral tissue, inhibiting cellular glucose intake and inducing insulin resistance. More research is required to understand these paraneoplastic phenomenon caused by diabetogenic tumor-secreted product in pancreatic cancer associated diabetes.


Sign in / Sign up

Export Citation Format

Share Document