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Background And Aims: Pancreatic acinar cell carcinoma (PACC) is rare. This study aims to elucidate its clinical features and survival outcomes.
Methods: Patients diagnosed with PACC were enrolled. A comparison between PACC and pancreatic ductal adenocarcinoma (PDAC) patients was conducted following propensity score matching (PSM).
Results: There were 11 resectable and nine unresectable PACC. The majority (60%) of PACC cases were located in the pancreatic head, with a median tumor size of 5.9 cm. Elevated serum lipase level was observed in 64.3% of cases. Regional lymph node involvement was found in 65.0%. The median survival was 20.0 months for resectable PACC patients compared to 6.7 months for unresectable cases. The 1-, 3-, and 5-year survival rates were 100%, 49.1%, and 32.0%, respectively, for resectable PACC patients, while for unresectable cases, they were 33.3%, 0%, and 0%. Resectable PACC patients exhibited lower rates of lymph node involvement (36.4% vs. 66.1%), lymphovascular invasion (LVI), 36.4% versus 72.8%, and perineural invasion (PNI), 45.5% versus 86.0%, compared to PDAC. Following PSM, there was no significant difference in survival between resectable PACC and PDAC.
Conclusion: PACC is associated with lower rates of lymph node involvement, LVI, and PNI, which might attribute to superior outcome when compared with PDAC reported in the literature. However, there is no survival difference between resecrable PACC and PDAC after PSM.
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http://dx.doi.org/10.1002/hsr2.70633 | DOI Listing |
Pulmonary adenoid cystic carcinoma (PACC) is a rare salivary gland-type malignancy of the tracheobronchial tree, accounting for 0.04%-0.2% of primary lung cancers.
View Article and Find Full Text PDFJ Surg Res
July 2025
Division of Surgical Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania. Electronic address:
Introduction: Pancreatic acinar cell carcinoma (pACC) and pancreatoblastoma (PBL) are rare pancreatic neoplasms with overlapping clinical and histological features. This study aims to compare the clinical presentation, treatment strategies, and survival outcomes of pACC and PBL using data from the National Cancer Database.
Methods: Data from the National Cancer Database (2004-2019) were analyzed for adult patients with pACC (n = 1416) and PBL (n = 32).
J Gastrointest Oncol
April 2025
Department of Gastroenterology, Hiroshima University Hospital, Hiroshima, Japan.
Background: Pancreatic acinar cell carcinoma (PACC) is a rare subtype of pancreatic cancer, and its clinicopathological behavior is not fully understood because of its rarity. The excision of the tumor is the best treatment, but PACC patients often have distant metastasis at the time of first diagnosis and sometimes have relapse after surgery. Thus, appropriate anti-tumor agents need to be administered; however, there is still no standard chemotherapy regimen for PACC.
View Article and Find Full Text PDFPediatr Dev Pathol
May 2025
Department of Pathology, University of Michigan, Michigan Medicine, Ann Arbor, MI, USA.
Pediatric pancreatic acinar cell carcinoma (PACC) is a rare malignancy, comprising 5-15% of pediatric pancreatic tumors. rearrangement is found in 20%-30% of PACC cases. We report a case of PACC with a novel fusion and independent amplifications in and .
View Article and Find Full Text PDFCancer Diagn Progn
May 2025
AntiCancer Inc., San Diego, CA, U.S.A.
Background/aim: Peritoneal carcinomatosis is the end stage for patients with gastrointestinal cancer, with survival ranging between 2 and 9 months. Pancreatic acinar cell carcinoma (PACC) is rare and can result in peritoneal metastases. The efficacy of chemotherapy for patients with PACC is unknown, and a systemic treatment strategy has not been established.
View Article and Find Full Text PDF