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原发性可切除胰腺癌的新辅助治疗:肿瘤学结局的系统评价和符合PRISMA标准的最新荟萃分析

Neo-Adjuvant Treatment in Primary Resectable Pancreatic Cancer: A Systematic Review and PRISMA-Compliant Updated Metanalysis of Oncological Outcomes.

作者信息

Roesel Raffaello, Deantonio Letizia, Bernardi Lorenzo, Garo Maria Luisa, Majno-Hurst Pietro, Vannelli Alberto, Cefalì Marco, Palmarocchi Maria Celeste, Valli Maria Carla, Pesola Guido, Cristaudi Alessandra, De Dosso Sara

机构信息

Department of Visceral Surgery, Hospital of Lugano (EOC), 6900 Lugano, Switzerland.

Radiation Oncology Department, Oncology Institute of Southern Switzerland (IOSI), EOC, 6500 Bellinzona, Switzerland.

出版信息

Cancers (Basel). 2023 Sep 19;15(18):4627. doi: 10.3390/cancers15184627.


DOI:10.3390/cancers15184627
PMID:37760596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10526896/
Abstract

BACKGROUND: Despite advances in treatment, the prognosis of resectable pancreatic adenocarcinoma remains poor. Neoadjuvant therapy (NAT) has gained great interest in hopes of improving survival. However, the results of available studies based on different treatment approaches, such as chemotherapy and chemoradiotherapy, showed contrasting results. The aim of this systematic review and meta-analysis is to clarify the benefit of NAT compared to upfront surgery (US) in primarily resectable pancreatic adenocarcinoma. METHODS: A PRISMA literature review identified 139 studies, of which 15 were finally included in the systematic review and meta-analysis. All data from eligible articles was summarized in a systematic summary and then used for the meta-analysis. Specifically, we used HR for OS and DFS and risk estimates (odds ratios) for the R0 resection rate and the N+ rate. The risk of bias was correctly assessed according to the nature of the studies included. RESULTS: From the pooled HRs, OS for NAT patients was better, with an HR for death of 0.80 (95% CI: 0.72-0.90) at a significance level of less than 1%. In the sub-group analysis, no difference was found between patients treated with chemoradiotherapy or chemotherapy exclusively. The meta-analysis of seven studies that reported DFS for NAT resulted in a pooled HR for progression of 0.66 (95% CI: 0.56-0.79) with a significance level of less than 1%. A significantly lower risk of positive lymph nodes (OR: 0.45; 95% CI: 0.32-0.63) and an improved R0 resection rate (OR: 1.70; 95% CI: 1.23-2.36) were also found in patients treated with NAT, despite high heterogeneity. CONCLUSIONS: NAT is associated with improved survival for patients with resectable pancreatic adenocarcinoma; however, the optimal treatment strategy has yet to be defined, and further studies are required.

摘要

背景:尽管治疗取得了进展,但可切除胰腺腺癌的预后仍然很差。新辅助治疗(NAT)因有望提高生存率而备受关注。然而,基于不同治疗方法(如化疗和放化疗)的现有研究结果却相互矛盾。本系统评价和荟萃分析的目的是阐明在原发性可切除胰腺腺癌中,与直接手术(US)相比,NAT的益处。 方法:通过PRISMA文献综述确定了139项研究,其中15项最终纳入系统评价和荟萃分析。符合条件的文章中的所有数据都汇总在一个系统总结中,然后用于荟萃分析。具体而言,我们使用总生存期(OS)和无病生存期(DFS)的风险比(HR)以及R0切除率和N+率的风险估计值(比值比)。根据纳入研究的性质正确评估偏倚风险。 结果:从汇总的HR来看,NAT患者的OS更好,死亡HR为0.80(95%可信区间:0.72-0.90),显著性水平小于1%。在亚组分析中,单纯接受放化疗或化疗的患者之间未发现差异。对7项报告NAT患者DFS的研究进行的荟萃分析得出,进展的汇总HR为0.66(95%可信区间:0.56-0.79),显著性水平小于1%。在接受NAT治疗的患者中,尽管异质性较高,但也发现阳性淋巴结风险显著降低(比值比:0.45;95%可信区间:0.32-0.63),R0切除率有所提高(比值比:1.70;95%可信区间:1.23-2.36)。 结论:NAT与可切除胰腺腺癌患者生存率的提高相关;然而,最佳治疗策略尚未确定,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/0e27ef54146c/cancers-15-04627-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1b3a3f2f7192/cancers-15-04627-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1bf8ec7ebdc2/cancers-15-04627-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/4c9dd84eb718/cancers-15-04627-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/b0d8055ac44a/cancers-15-04627-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/09b3295118df/cancers-15-04627-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1cfaf66639e4/cancers-15-04627-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/0e27ef54146c/cancers-15-04627-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1b3a3f2f7192/cancers-15-04627-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1bf8ec7ebdc2/cancers-15-04627-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/4c9dd84eb718/cancers-15-04627-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/b0d8055ac44a/cancers-15-04627-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/09b3295118df/cancers-15-04627-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/1cfaf66639e4/cancers-15-04627-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9633/10526896/0e27ef54146c/cancers-15-04627-g007.jpg

相似文献

[1]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Neoadjuvant therapy versus upfront surgery approach in resectable pancreatic cancer: a systematic review and meta-analysis.

Ann Gastroenterol. 2025

[2]
Neoadjuvant and Adjuvant Chemotherapy for Pancreatic Adenocarcinoma: Literature Review and Our Experience of NAC-GS.

Cancers (Basel). 2024-2-23

[3]
Pancreaticoduodenectomies with Concurrent Colectomies: Indications, Technical Issues, Complications, and Oncological Outcomes.

J Clin Med. 2023-12-14

本文引用的文献

[1]
Does neoadjuvant treatment in resectable pancreatic cancer improve overall survival? A systematic review and meta-analysis of randomized controlled trials.

ESMO Open. 2023-2

[2]
Perioperative or only adjuvant gemcitabine plus nab-paclitaxel for resectable pancreatic cancer (NEONAX)-a randomized phase II trial of the AIO pancreatic cancer group.

Ann Oncol. 2023-1

[3]
Neoadjuvant chemotherapy with or without radiotherapy versus upfront surgery for resectable pancreatic adenocarcinoma: a meta-analysis of randomized clinical trials.

ESMO Open. 2022-6

[4]
Neoadjuvant Chemoradiotherapy Versus Upfront Surgery for Resectable and Borderline Resectable Pancreatic Cancer: Long-Term Results of the Dutch Randomized PREOPANC Trial.

J Clin Oncol. 2022-4-10

[5]
Prognosis and survival analysis of patients with pancreatic cancer: retrospective experience of a single institution.

World J Surg Oncol. 2022-1-7

[6]
Neoadjuvant Therapy for Resectable Pancreatic Cancer: A New Standard of Care. Pooled Data From 3 Randomized Controlled Trials.

Ann Surg. 2021-11-1

[7]
Response to Neoadjuvant Therapy and Prognosis in Patients with Resectable Pancreatic Cancer: A Propensity Score Matching Analysis.

Gut Liver. 2022-1-15

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Pancreatic Adenocarcinoma, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.

J Natl Compr Canc Netw. 2021-4-1

[9]
Total neoadjuvant FOLFIRINOX versus neoadjuvant gemcitabine-based chemoradiotherapy and adjuvant gemcitabine for resectable and borderline resectable pancreatic cancer (PREOPANC-2 trial): study protocol for a nationwide multicenter randomized controlled trial.

BMC Cancer. 2021-3-23

[10]
Predictive factors for long-term survival after surgery for pancreatic ductal adenocarcinoma: Making a case for standardized reporting of the resection margin using certified cancer center data.

PLoS One. 2021

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