Literature DB >> 29387696

The borderline resectable and locally advanced pancreatic ductal adenocarcinoma: Definition.

Assaad M Soweid1.   

Abstract

Entities:  

Year:  2017        PMID: 29387696      PMCID: PMC5774079          DOI: 10.4103/eus.eus_66_17

Source DB:  PubMed          Journal:  Endosc Ultrasound        ISSN: 2226-7190            Impact factor:   5.628


× No keyword cloud information.

INTRODUCTION

Pancreatic ductal adenocarcinoma (PDAC) is the fourth most common cause of cancer death in the United States with around 50,000 incident cases and 40,000 deaths in 2015.[1] Despite the tremendous recent advances in diagnostic and therapeutic interventions, the 5-year survival rate remains dismal at approximately 5%. At initial presentation, the majority of patients (50%–55%) have metastatic disease while only 20% have resectable disease.[23] The remaining 25%–30% of patients present with either borderline resectable (BR) or locally advanced (LA) disease.[24] In both BR-PDAC and LA-PDAC, the tumor is localized to the pancreas but adheres to or invades adjacent vascular structures, including the celiac axis (CA) vessels, superior mesenteric artery (SMA), superior mesenteric vein (SMV), and portal vein (PV). Patients with BR-PDAC and LA-PDAC represent a unique subset of patients with PDAC who are not candidates for primary surgical resection. Identification of such patients requires a team of experts in the fields of gastroenterology/endosonography and radiology (computed tomography, magnetic resonance imaging). This identification is vital for the planning of a potentially curative multimodality treatment that relies on chemotherapy, radiotherapy (RT), and surgery. The objective of treatment for BR-PDAC is to achieve tumor downstaging to facilitate margin-negative (R0) resection, while that for LA-PDAC is local disease control with improvement of survival.

BR-PDAC

Over the past decade, the concept of “BR” PDAC has emerged to describe a distinct spectrum of patients ranging from “resectable” to LA disease, for whom a microscopically margin-positive (R1) resection is considered relatively more likely, primarily due to the relationship between the primary pancreatic tumor and the surrounding blood vessels. Unfortunately, both anatomic and imaging criteria to define “borderline resectability” are not yet universally agreed upon, with several classification systems proposed in the literature and considerable variability among medical institutions. Thus, as a result of: the lack of consensus regarding the definition, the relatively small numbers of patients in this category, and the paucity of dedicated clinical trials; accurate evidence-based diagnostic categorization and treatment selection for this subgroup of patients remains a major challenge. Hence, although there is no consensus regarding the definition, BR-PDAC is often defined as a tumor confined to the pancreatic bed with limited involvement of the adjacent vascular structures where vascular reconstruction options are feasible.[4] However, there is not yet a universally accepted definition in the oncology community regarding the extent of vascular involvement that would be amenable to reconstruction.[56] More specifically, according to the Society of Surgical Oncology/American Hepato-Pancreato-Biliary Association/Society for Surgery of the Alimentary Tract consensus definition, which had been incorporated into the National Comprehensive Cancer Network (NCCN) guidelines, BR tumors have: (a) no distant metastases; (b) venous involvement of the SMV/PV with or without impingement and narrowing of the lumen; (c) short segment venous occlusion but with suitable vessel proximal and distal to occlusion, allowing for safe resection and reconstruction; (d) gastroduodenal artery (GDA) encasement up to the hepatic artery (HA) with either short segment encasement or direct abutment of HA, without extension to the CA; and (e) tumor abutment of the SMA not to exceed 180° of the circumference.[5678] To complicate matters further, there is even internal conflict within the individual consensus statements. For example, it is noted in the 2016 NCCN guidelines that there is disagreement among various panelists regarding the second celiac criterion (>180° contact without involvement of the aorta and with intact and uninvolved GDA), which some would deem unresectable.[79] A growing body of evidence suggests that the BR group may particularly benefit from neoadjuvant therapy to increase the likelihood of a margin-negative (R0) resection. Recent data have revealed that PDAC patients with involvement of the adjacent mesenteric vessels who were undergoing R0 resections had the same survival outcomes as those who underwent resection for primarily resectable PDAC.[1011] The main challenge in the surgical management of BR-PDAC is the high rate of positive margins at the reconstructed vessel segments, leading to high risk of local and systemic recurrence.[12] Selection of patients who will benefit from neoadjuvant therapy or upfront surgical resection is a particularly challenging task that is highly dependent on the expertise of the multidisciplinary team members.

LA-PDAC

On the other hand, LA-PDAC is often defined as the involvement of the CA or the encasement of >180° of the SMA (T4) and/or involvement of SMV/PV with no reconstruction options, irrespective of nodal involvement, provided that no distant metastasis exists outside the pancreatic bed.[13] Historically, BR-PDAC has been included in trials that involved LA-PDAC patients. The median overall survival ranges from 5.5 to 22 months (LA-PDAC around 16 months, whereas BR-PDAC rarely reaches 2 years).[31314151617] Optimal treatment for BR-PDAC is still controversial with regard to the type, dose, and regimen of chemotherapy, use of RT, RT field and dose, and sequence of the multimodality treatment approach. The chance of surgical resection in patients with LA-PDAC is <5%. LA-PDAC is often treated with combination chemotherapy or combined chemoradiation therapy. These approaches have not shown any improvement in survival.[1617]

CONCLUSIONS

It is very important to recognize and closely follow the evolving imaging criteria for defining BR and LA disease given their profound implications for treatment strategy, follow-up recommendations, and overall prognosis.
  16 in total

1.  Meta-analyses of chemotherapy for locally advanced and metastatic pancreatic cancer.

Authors:  Asma Sultana; Catrin Tudur Smith; David Cunningham; Naureen Starling; John P Neoptolemos; Paula Ghaneh
Journal:  J Clin Oncol       Date:  2007-06-20       Impact factor: 44.544

2.  Pretreatment assessment of resectable and borderline resectable pancreatic cancer: expert consensus statement.

Authors:  Mark P Callery; Kenneth J Chang; Elliot K Fishman; Mark S Talamonti; L William Traverso; David C Linehan
Journal:  Ann Surg Oncol       Date:  2009-04-24       Impact factor: 5.344

3.  FOLFIRINOX in locally advanced pancreatic cancer: the Massachusetts General Hospital Cancer Center experience.

Authors:  Jason E Faris; Lawrence S Blaszkowsky; Shaunagh McDermott; Alexander R Guimaraes; Jackie Szymonifka; Mai Anh Huynh; Cristina R Ferrone; Jennifer A Wargo; Jill N Allen; Lauren E Dias; Eunice L Kwak; Keith D Lillemoe; Sarah P Thayer; Janet E Murphy; Andrew X Zhu; Dushyant V Sahani; Jennifer Y Wo; Jeffrey W Clark; Carlos Fernandez-del Castillo; David P Ryan; Theodore S Hong
Journal:  Oncologist       Date:  2013-05-08

4.  Length and quality of survival after external-beam radiotherapy with concurrent continuous 5-fluorouracil infusion for locally unresectable pancreatic cancer.

Authors:  Hiroyuki Shinchi; Sonshin Takao; Hidetoshi Noma; Yoichiro Matsuo; Yuko Mataki; Shinichiro Mori; Takashi Aikou
Journal:  Int J Radiat Oncol Biol Phys       Date:  2002-05-01       Impact factor: 7.038

5.  Cancer statistics, 2015.

Authors:  Rebecca L Siegel; Kimberly D Miller; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2015-01-05       Impact factor: 508.702

6.  Neoadjuvant modified (m) FOLFIRINOX for locally advanced unresectable (LAPC) and borderline resectable (BRPC) adenocarcinoma of the pancreas.

Authors:  Marlo Blazer; Christina Wu; Richard M Goldberg; Gary Phillips; Carl Schmidt; Peter Muscarella; Evan Wuthrick; Terrence M Williams; Joshua Reardon; E Christopher Ellison; Mark Bloomston; Tanios Bekaii-Saab
Journal:  Ann Surg Oncol       Date:  2014-10-31       Impact factor: 5.344

7.  A randomized phase III study of radiotherapy alone or with 5-fluorouracil and mitomycin-C in patients with locally advanced adenocarcinoma of the pancreas: Eastern Cooperative Oncology Group study E8282.

Authors:  Steven J Cohen; Ralph Dobelbower; Stuart Lipsitz; Paul J Catalano; Benjamin Sischy; Thomas J Smith; Daniel G Haller
Journal:  Int J Radiat Oncol Biol Phys       Date:  2005-08-01       Impact factor: 7.038

Review 8.  Borderline resectable pancreatic cancer: definitions, management, and role of preoperative therapy.

Authors:  Gauri R Varadhachary; Eric P Tamm; James L Abbruzzese; Henry Q Xiong; Christopher H Crane; Huamin Wang; Jeffrey E Lee; Peter W T Pisters; Douglas B Evans; Robert A Wolff
Journal:  Ann Surg Oncol       Date:  2006-07-24       Impact factor: 5.344

Review 9.  Contemporary Management of Borderline Resectable and Locally Advanced Unresectable Pancreatic Cancer.

Authors:  Walid L Shaib; Andrew Ip; Kenneth Cardona; Olatunji B Alese; Shishir K Maithel; David Kooby; Jerome Landry; Bassel F El-Rayes
Journal:  Oncologist       Date:  2016-02-01

10.  5-Fluorouracil, methyl-CCNU, and radiotherapy with or without testolactone for localized adenocarcinoma of the exocrine pancreas: a Southwest Oncology Group Study.

Authors:  J D McCracken; P Ray; L K Heilbrun; V K Vaitkevicius; J H Saiki; S E Rivkin; A H Rossof; T N Moore
Journal:  Cancer       Date:  1980-10-01       Impact factor: 6.860

View more
  3 in total

1.  Consensus in determining the resectability of locally progressed pancreatic ductal adenocarcinoma - results of the Conko-007 multicenter trial.

Authors:  U A Wittel; D Lubgan; M Ghadimi; O Belyaev; W Uhl; W O Bechstein; R Grützmann; W M Hohenberger; A Schmid; L Jacobasch; R S Croner; A Reinacher-Schick; U T Hopt; A Pirkl; H Oettle; R Fietkau; H Golcher
Journal:  BMC Cancer       Date:  2019-10-22       Impact factor: 4.430

2.  Keratin 17 testing in pancreatic cancer needle aspiration biopsies predicts survival.

Authors:  Lucia Roa-Peña; Sruthi Babu; Cindy V Leiton; Maoxin Wu; Sofia Taboada; Ali Akalin; Jonathan Buscaglia; Luisa F Escobar-Hoyos; Kenneth R Shroyer
Journal:  Cancer Cytopathol       Date:  2021-06-02       Impact factor: 4.264

Review 3.  A Review on the Efficacy and Safety of Nab-Paclitaxel with Gemcitabine in Combination with Other Therapeutic Agents as New Treatment Strategies in Pancreatic Cancer.

Authors:  Christian Chapa-González; Karina López; Kimberly Michelle Lomelí; Jorge Alberto Roacho-Pérez; Jazmín Cristina Stevens
Journal:  Life (Basel)       Date:  2022-02-22
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.