Relationships between postoperative recurrences and standardized uptake value on 18F-fluorodeoxyglucose-positron emission tomography in patients with resectable and borderline resectable pancreatic ductal adenocarcinoma who underwent curative pancreatic resection after neoadjuvant chemoradiotherapy.

IF 2.8 2区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Hironobu Suto, Mina Nagao, Hiroyuki Matsukawa, Takuro Fuke, Yasuhisa Ando, Minoru Oshima, Shigeo Takahashi, Toru Shibata, Hideki Kamada, Hideki Kobara, Hiroyuki Okuyama, Tomohiro Hirao, Kensuke Kumamoto, Keiichi Okano
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引用次数: 0

Abstract

Background: This study aimed to examine postoperative recurrence after curative pancreatic resection following neoadjuvant chemoradiotherapy (NACRT) in patients with resectable (R-) and borderline resectable (BR-) pancreatic ductal adenocarcinoma (PDAC), focusing on its relationship with the standardized uptake value (SUV) on 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET).

Method: The postoperative initial recurrence patterns were examined in patients with R- and BR-PDAC who underwent NACRT followed by curative pancreatic resection. Data collected from three prospective clinical trials were retrospectively analysed.

Results: After a median follow-up of 29 months, 91 (60 %) of 151 patients experienced postoperative recurrence. The median recurrence-free survival (RFS) for all patients was 18 months. The sites of first recurrence were lung-only in 24 (26 %) patients, liver-only in 23 (25 %), local-only in 11 (12 %), peritoneum-only in 10 (11 %), other single site in 5 (5 %), and multiple sites in 19 (21 %) patients. Multivariate analysis identified the maximum standardized uptake value (SUVmax) on FDG-PET at diagnoses ≥5.40 (hazard ratio [HR], 1.62; 95 % confidence interval [CI], 1.01-2.61; p = 0.045) and node-positive pathology (HR, 2.01; 95 % CI, 1.32-3.08; p = 0.001) as significant predictors of RFS. Furthermore, the SUVmax at initial diagnosis and after NACRT correlated with liver metastasis.

Conclusion: R- and BR-PDACs with high SUV on FDG-PET at diagnosis are risk factors for postoperative recurrence. Among patients who undergo surgery after NACRT, those with a high SUVmax at diagnosis or post-NACRT require careful attention for postoperative liver recurrence.

新辅助化放疗后接受胰腺根治性切除术的可切除和边缘可切除胰腺导管腺癌患者术后复发与 18F- 氟脱氧葡萄糖-正电子发射断层扫描标准化摄取值之间的关系。
研究背景本研究旨在探讨可切除(R-)和边缘可切除(BR-)胰腺导管腺癌(PDAC)患者在接受新辅助化放疗(NACRT)后进行胰腺根治性切除术后的术后复发情况,重点研究其与18F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)的标准化摄取值(SUV)之间的关系:方法:研究了R-和BR-PDAC患者的术后初始复发模式,这些患者接受了NACRT治疗,随后进行了胰腺根治性切除术。对三项前瞻性临床试验收集的数据进行了回顾性分析:中位随访 29 个月后,151 例患者中有 91 例(60%)术后复发。所有患者的中位无复发生存期(RFS)为18个月。首次复发部位分别为:24(26%)例患者仅肺部复发,23(25%)例患者仅肝部复发,11(12%)例患者仅局部复发,10(11%)例患者仅腹膜复发,5(5%)例患者为其他单一部位复发,19(21%)例患者为多部位复发。多变量分析发现,诊断时 FDG-PET 最大标准化摄取值(SUVmax)≥5.40(危险比 [HR],1.62;95% 置信区间 [CI],1.01-2.61;P = 0.045)和结节阳性病理(HR,2.01;95% CI,1.32-3.08;P = 0.001)是 RFS 的重要预测因素。此外,初诊时和NACRT后的SUVmax与肝转移相关:结论:诊断时FDG-PET SUV较高的R-和BR-PDAC是术后复发的危险因素。结论:诊断时FDG-PET SUV值高的R-和BR-PDAC是术后复发的危险因素,在NACRT后接受手术的患者中,诊断时或NACRT后SUVmax值高的患者需要小心术后肝脏复发。
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来源期刊
Pancreatology
Pancreatology 医学-胃肠肝病学
CiteScore
7.20
自引率
5.60%
发文量
194
审稿时长
44 days
期刊介绍: Pancreatology is the official journal of the International Association of Pancreatology (IAP), the European Pancreatic Club (EPC) and several national societies and study groups around the world. Dedicated to the understanding and treatment of exocrine as well as endocrine pancreatic disease, this multidisciplinary periodical publishes original basic, translational and clinical pancreatic research from a range of fields including gastroenterology, oncology, surgery, pharmacology, cellular and molecular biology as well as endocrinology, immunology and epidemiology. Readers can expect to gain new insights into pancreatic physiology and into the pathogenesis, diagnosis, therapeutic approaches and prognosis of pancreatic diseases. The journal features original articles, case reports, consensus guidelines and topical, cutting edge reviews, thus representing a source of valuable, novel information for clinical and basic researchers alike.
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