Lymphatic Invasion is an Independent Prognostic Factor in Pancreatic Cancer Patients Undergoing Curative Resection Followed by Adjuvant Chemotherapy with Gemcitabine or S-1

被引:6
作者
Aoyama, Toru [1 ]
Murakawa, Masaaki [1 ]
Katayama, Yusuke [1 ]
Shiozawa, Manabu [1 ]
Ueno, Makoto [2 ]
Morimoto, Manabu [2 ]
Yoshikawa, Takaki [3 ]
Rino, Yasushi [3 ]
Masuda, Munetaka [3 ]
Morinaga, Soichiro [1 ]
机构
[1] Kanagawa Canc Ctr, Dept Gastrointestinal Surg, Yokohama, Kanagawa 2418515, Japan
[2] Kanagawa Canc Ctr, Dept Gastrointestinal Med, Yokohama, Kanagawa 2418515, Japan
[3] Yokohama City Univ, Dept Surg, Yokohama, Kanagawa, Japan
关键词
Pancreatic cancer; Lymphatic invasion; Adjuvant chemotherapy; SURVIVAL; ADENOCARCINOMA; RECURRENCE; TRIAL;
D O I
10.5754/hge14949
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The objective of this retrospective Study was to clarify prognostic factors in pancreatic cancer patients undergoing curative resection. followed by adjuvant chemotherapy with gemcitabine or S-1. Methodology: Both overall survival (OS) and recurrence-free survival (RFS) were examined in 122 pancreatic cancer patients who underwent curative surgery and received adjuvant gemcitabine, or S-1 after surgery between 2005 and 2014. Results: When the length of OS was evaluated according to the log-rank test, significant differences were observed in lymphatic invasion and the T status. Univariate and multivariate Cox's proportional hazard analyses demonstrated that lymphatic invasion was the only significant independent prognostic factor for both OS and: RFS. The 5-year OS was 30.1% in the lymphatic invasion-negative group and 12.1% in the lymphatic invasion-positive group (p<0.001). Moreover, the 5-year RFS was 20.5% in the lymphatic invasion-negative group and 10.4% in the lymphatic invasion-positive group (p=0.006). Conclusions: Lymphatic invasion is the most important prognostic factor for OS and RFS in patients with pancreatic cancer who undergo curative resection followed by adjuvant chemotherapy The present results suggest that adjuvant chemotherapy is not sufficient, especially in patients with risk factors. Such patients should be evaluated as a target group for clinical trials of novel treatments.
引用
收藏
页码:472 / 477
页数:6
相关论文
共 17 条
[1]  
[Anonymous], 2020, CA Cancer J Clin, DOI DOI 10.3322/CAAC.21590
[2]  
[Anonymous], 2013 GASTR CANC S
[3]   Tumor size is the primary prognosticator for pancreatic cancer after regional pancreatectomy [J].
Fortner, JG ;
Klimstra, DS ;
Senie, RT ;
Maclean, BJ .
ANNALS OF SURGERY, 1996, 223 (02) :147-153
[4]   Analysis of mortality rates for pancreatic cancer across the world [J].
Hariharan, D. ;
Saied, A. ;
Kocher, H. M. .
HPB, 2008, 10 (01) :58-62
[5]   Patterns of recurrence after curative resection of pancreatic cancer, based on autopsy findings [J].
Hishinuma, S ;
Ogata, Y ;
Tomikawa, M ;
Ozawa, I ;
Hirabayashi, K ;
Igarashi, S .
JOURNAL OF GASTROINTESTINAL SURGERY, 2006, 10 (04) :511-518
[6]  
Klein Fritz, 2014, HPB Surg, V2014, P970234, DOI 10.1155/2014/970234
[7]   Surgical treatment of pancreatic adenocarcinoma: actual survival and prognostic factors in 343 patients [J].
Kuhlmann, KFCD ;
de Castro, SMM ;
Wesseling, JG ;
ten Kate, FJW ;
Offerhaus, GJA ;
Busch, ORC ;
van Gulik, TM ;
Obertop, H ;
Gouma, DJ .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (04) :549-558
[8]   Breast cancer resistance protein expression is associated with early recurrence and decreased survival in resectable pancreatic cancer patients [J].
Lee, Sang Hyub ;
Kim, Haeryoung ;
Hwang, Jin-Hyeok ;
Lee, Hye Seung ;
Cho, Jai Young ;
Yoon, Yoo-Seok ;
Han, Ho-Seong .
PATHOLOGY INTERNATIONAL, 2012, 62 (03) :167-175
[9]   Predicting survival after surgical resection for pancreatic ductal adenocarcinoma [J].
Moon, HJ ;
An, JY ;
Heo, JS ;
Choi, SH ;
Joh, JW ;
Kim, YI .
PANCREAS, 2006, 32 (01) :37-43
[10]   Adjuvant Chemotherapy With Fluorouracil Plus Folinic Acid vs Gemcitabine Following Pancreatic Cancer Resection A Randomized Controlled Trial [J].
Neoptolemos, John P. ;
Stocken, Deborah D. ;
Bassi, Claudio ;
Ghaneh, Paula ;
Cunningham, David ;
Goldstein, David ;
Padbury, Robert ;
Moore, Malcolm J. ;
Gallinger, Steven ;
Mariette, Christophe ;
Wente, Moritz N. ;
Izbicki, Jakob R. ;
Friess, Helmut ;
Lerch, Markus M. ;
Dervenis, Christos ;
Olah, Attila ;
Butturini, Giovanni ;
Doi, Ryuichiro ;
Lind, Pehr A. ;
Smith, David ;
Valle, Juan W. ;
Palmer, Daniel H. ;
Buckels, John A. ;
Thompson, Joyce ;
McKay, Colin J. ;
Rawcliffe, Charlotte L. ;
Buechler, Markus W. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2010, 304 (10) :1073-1081