TY - JOUR
T1 - Comparison of Ampullary and Pancreatic Adenocarcinomas
T2 - Smaller Invasion, Common Adenomatous Components, Resectability, and Histology are Factors for Improved Survival for Patients with Ampullary Adenocarcinoma
AU - Memis, Bahar
AU - Saka, Burcu
AU - Pehlivanoglu, Burcin
AU - Kim, Grace
AU - Balci, Serdar
AU - Tajiri, Takuma
AU - Ohike, Nobuyuki
AU - Bagci, Pelin
AU - Akar, Kadriye Ebru
AU - Muraki, Takashi
AU - Jang, Kee Taek
AU - Maithel, Shishir K.
AU - Sarmiento, Juan
AU - Kooby, David A.
AU - Esmer, Rohat
AU - Tarcan, Zeynep Cagla
AU - Goodman, Michael
AU - Xue, Yue
AU - Krasinskas, Alyssa
AU - Reid, Michelle
AU - Basturk, Olca
AU - Adsay, Volkan
N1 - Publisher Copyright:
© Society of Surgical Oncology 2024.
PY - 2024
Y1 - 2024
N2 - Background: The information on the clinicopathologic/outcome differences between ampullary adenocarcinoma (AC) and pancreatic adenocarcinoma (PC) has been conflicting to the extent that it still is questioned whether ACs need to be recognized separately from PCs. Methods: The characteristics of 413 ACs were compared with those of 547 PCs. Results: The ACs had a better prognosis than the PCs (5-year survival, 57 % vs 23 %; p < 0.001). Even the pancreatobiliary (PB)-type ACs had a better prognosis (5-year survival, 46 % vs 23 %; p < 0.001). Several differences also were identified as contributing factors: (1) the preinvasive adenomatous component often constituted a significant proportion of the mass in ACs (>50 % of the tumor in 16 % vs 1.5 %; p < 0.001); (2) the mean size of the carcinoma was smaller in ACs (2.5 vs 3.2 cm; p < 0.001): when matched for invasion size, the survival advantage of AC was minimized, and when matched for invasion size larger than 2 cm, the survival advantage of AC lost its statistical significance; (3) lymph node (LN) metastases were less common in ACs (49 % vs 71 %; p < 0.001); (4) the definitive R1 rate was lower in ACs (4 % vs 23.5 %; p < 0.001); and (5) non-PB and non-tubular adenocarcinoma types were more common in ACs (17 % vs 3 %; p < 0.001). Conclusions: Comparatively, ACs have better clinical survival than PCs. Potential contributing factors are the relative abundance of the preinvasive component, smaller invasion, lower LN metastasis rate, higher resectability, and common occurrence of less aggressive histologic phenotypes (intestinal, medullary, mucinous). However, this survival advantage is sustained even in PB-type ACs, highlighting the importance of accurately determining the site of origin.
AB - Background: The information on the clinicopathologic/outcome differences between ampullary adenocarcinoma (AC) and pancreatic adenocarcinoma (PC) has been conflicting to the extent that it still is questioned whether ACs need to be recognized separately from PCs. Methods: The characteristics of 413 ACs were compared with those of 547 PCs. Results: The ACs had a better prognosis than the PCs (5-year survival, 57 % vs 23 %; p < 0.001). Even the pancreatobiliary (PB)-type ACs had a better prognosis (5-year survival, 46 % vs 23 %; p < 0.001). Several differences also were identified as contributing factors: (1) the preinvasive adenomatous component often constituted a significant proportion of the mass in ACs (>50 % of the tumor in 16 % vs 1.5 %; p < 0.001); (2) the mean size of the carcinoma was smaller in ACs (2.5 vs 3.2 cm; p < 0.001): when matched for invasion size, the survival advantage of AC was minimized, and when matched for invasion size larger than 2 cm, the survival advantage of AC lost its statistical significance; (3) lymph node (LN) metastases were less common in ACs (49 % vs 71 %; p < 0.001); (4) the definitive R1 rate was lower in ACs (4 % vs 23.5 %; p < 0.001); and (5) non-PB and non-tubular adenocarcinoma types were more common in ACs (17 % vs 3 %; p < 0.001). Conclusions: Comparatively, ACs have better clinical survival than PCs. Potential contributing factors are the relative abundance of the preinvasive component, smaller invasion, lower LN metastasis rate, higher resectability, and common occurrence of less aggressive histologic phenotypes (intestinal, medullary, mucinous). However, this survival advantage is sustained even in PB-type ACs, highlighting the importance of accurately determining the site of origin.
KW - Ampulla
KW - Carcinoma
KW - Histologic phenotype
KW - Metastasis
KW - Pancreas
KW - Size
KW - Stage
KW - Survival
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U2 - 10.1245/s10434-024-16355-w
DO - 10.1245/s10434-024-16355-w
M3 - Article
C2 - 39402320
AN - SCOPUS:85206688099
SN - 1068-9265
JO - Annals of surgical oncology
JF - Annals of surgical oncology
ER -