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Optimal Preoperative Multidisciplinary Treatment in Borderline Resectable Pancreatic Cancer

Authors :
Fuminori Sonohara
Tsutomu Fujii
Yui Hoshino
Toru Watanabe
Kenta Murotani
Koshi Matsui
Kosuke Mori
Yasuhiro Kodera
Mitsuro Kanda
Nana Kimura
Tomoyuki Okumura
Kazuto Shibuya
Masamichi Hayashi
Hideki Takami
Takeshi Miwa
Katsuhisa Hirano
Suguru Yamada
Hayato Baba
Isaku Yoshioka
Source :
Cancers, Volume 13, Issue 1, Cancers, Vol 13, Iss 36, p 36 (2021)
Publication Year :
2020

Abstract

Background: The objective of this study was to investigate the optimal neoadjuvant therapy (NAT) for borderline resectable pancreatic cancer invading the portal vein (BR-PV) or abutting major arteries (BR-A). Methods: We retrospectively analyzed 88 patients with BR-PV and 111 patients with BR-A. Results: In BR-PV patients who underwent upfront surgery (n = 46)/NAT (n = 42), survival was significantly better in the NAT group (3-year overall survival (OS): 5.8%/35.5%, p = 0.004). In BR-A patients who underwent upfront surgery (n = 48)/NAT (n = 63), survival was also significantly better in the NAT group (3-year OS:15.5%/41.7%, p &lt<br />0.001). The prognosis tended to be better in patients who received newer chemotherapeutic regimens, such as FOLFIRINOX and gemcitabine with nab-paclitaxel. In 36 BR-PV patients who underwent surgery after NAT, univariate analysis revealed that normalization of tumor marker (TM) levels (p = 0.028) and preoperative high prognostic nutritional index (PNI) (p = 0.022) were significantly associated with a favorable prognosis. In 39 BR-A patients who underwent surgery after NAT, multivariate analysis revealed that preoperative PNI &gt<br />42.5 was an independent prognostic factor (HR: 0.15, p = 0.014). Conclusions: NAT using newer chemotherapy is essential for improving the prognosis of BR pancreatic cancer. These findings suggest that prognosis may be prolonged by maintaining good nutritional status during preoperative treatment.

Details

ISSN :
20726694
Volume :
13
Issue :
1
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....afd958b39665cb8f3e31341b0983ee59