Central pancreatectomy might be an acceptable surgical procedure for clinical T1 pancreatic body ductal adenocarcinoma: A multicenter retrospective analysis

被引:2
作者
Terai, Taichi [1 ]
Kawai, Manabu [2 ]
Kitahata, Yuji [2 ]
Satoi, Sohei [3 ,4 ]
Hashimoto, Daisuke [3 ]
Nagai, Minako [1 ]
Nishiwada, Satoshi [1 ]
Yamamoto, Tomohisa [3 ]
Yamaue, Hiroki [2 ]
Sho, Masayuki [1 ]
机构
[1] Nara Med Univ, Dept Surg, 840 Shijo Cho, Kashihara, Nara 6348522, Japan
[2] Wakayama Med Univ, Dept Surg 2, Wakayama, Japan
[3] Kansai Med Univ, Dept Surg, Hirakata, Osaka, Japan
[4] Univ Colorado, Div Surg Oncol, Anschutz Med Campus, Aurora, CO 80045 USA
关键词
central pancreatectomy; multicenter study; neoadjuvant therapy; organ preservation; pancreatic body cancer; DIABETES-MELLITUS; GEMCITABINE; CHEMOTHERAPY; CANCER; S-1;
D O I
10.1002/jhbp.1355
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Central pancreatectomy (CP) is accepted as a function-preserving procedure for benign tumors. However, the indication of CP for pancreatic cancers is limited. This multicenter study aimed to clarify the indications of CP for clinical T1 pancreatic body cancer.Methods: This multicenter study analyzed patients who underwent CP or distal pancreatectomy (DP) for clinical T1 pancreatic body cancer between 2013 and 2020 at three high-volume centers.Results: A total of 50 patients were enrolled: nine patients, who underwent CP, were classified into the CP group, while 38 patients, who underwent DP, served as controls. Three patients converted CP to DP during operation were excluded. Five patients in the CP group and 15 patients in the control group underwent preoperative treatment. The 5-year survival rate was 100% in the CP group, and 42% (p = .040) in the control group. Recurrence was found in three patients in the CP group. Importantly, insulin was not required after surgery in patients in the CP group.Conclusion: The clinical outcomes of CP were comparable to or even better than that of conventional pancreatectomy. Our collaborative study suggests that CP may be an acceptable therapeutic option for selected patients with clinical T1 pancreatic body cancer.
引用
收藏
页码:1334 / 1342
页数:9
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