Mikolaj Kowal
Andrew Smith
Sanjay Pandanaboyana
Samir Pathak- 1The Department of Hepatobiliary Surgery, St. James’s University Hospital, Leeds, United Kingdom
- 2Leeds Institute of Medical Research, Faculty of Medicine and Health, University of Leeds, Leeds, United Kingdom
- 3Hepato-Pancreato-Biliary and Transplant Unit, Freeman Hospital, Newcastle Upon Tyne, United Kingdom
Editorial on the Research Topic
Technological innovations and pancreatic cancer
Pancreatic ductal adenocarcinoma (PDAC) has poor survival outcomes. The main reasons include late presentation, resulting in only 20% of patients being eligible for surgery, and poor response to chemotherapy, secondary to the challenging tumour biology (1, 2). For patients undergoing surgery, the local anatomy and invasiveness of PDAC results in high operative risks, with morbidity and mortality estimated at 50-70% and 2-8%, respectively (3, 4). The incidence of PDAC is rising, making it the fourth leading cause of death in the United States (5). It is imperative to prioritise PDAC research. Technological advances may improve patient outcomes through early detection and optimisation of treatments. The editorial highlights the latest technological advances in PDAC and identifies areas for research (Figure 1).
Figure 1. Graphical representation of technological innovation in pancreatic ductal adenocarcinoma (PDAC). EUS, Endoscopic ultrasound; MIS, Minimally invasive surgery; RT, Radiotherapy.
Technological breakthroughs enabling early detection of PDAC were described in a review on liquid biopsy (6). This sampling method uses biomarkers such as circulating tumour DNA (ctDNA) and extracellular vesicles (EVs). Liquid biopsy is exciting due to its non-invasive, real-time and repeatable properties. Recent advances in methylation analysis, detecting epigenetic reprogramming in early tumorigenesis, have improved the detection of PDAC using ctDNA. A meta-analysis performed in 2019 showed sensitivity and specificity rates of 70% and 86% respectively. Another biomarker showing promise are EVs, with one study showing high sensitivity and specificity rates of 99% and 82% respectively. The current accuracy of liquid biopsy across all methods for PDAC was investigated in a meta-analysis (7). They concluded that liquid biopsy using biomarkers such as ctDNA was less accurate than CA19-9 for PDAC detection. However, ctDNA was associated with worse survival, making it a useful prognostication tool. Further research utilising multiple biomarkers may increase the accuracy in PDAC detection.
Advances in neoadjuvant chemotherapy regimens are enabling surgical treatment for patients with locally advanced PDAC. Zhang et al. documented the case of a patient with a locally advanced PDAC. Following six cycles of GEM-NabP chemotherapy the patient underwent surgery, with histology confirming near-complete response. Successes such as this are often attributed to favourable biology, but standardisation of neoadjuvant regimens may improve overall outcomes. Further improvements in neoadjuvant treatments are seen in combination with immunotherapy. Lu et al. published a case report of combined neoadjuvant treatment using a programmed cell death protein-1 inhibitor and chemoradiotherapy (8). Following neoadjuvant treatment for a locally advanced PDAC, the patient underwent a pylorus-preserving pancreaticoduodenectomy (PPPD) with histology showing a pathologic complete response. Further data is also showing the benefit of established adjuvant chemotherapy regimens. A retrospective cohort study by Choi et al. analysed outcomes for patients who received adjuvant chemotherapy for locally advanced PDAC. They showed that 5-fluorouracil-based regimens resulted in favourable survival. New advances have also been made in the delivery of chemotherapy. Cao et al. performed a meta-analysis of regional intra-arterial chemotherapy (RIAC) compared with systemic treatment. RIAC has been developed recently and trialled in PDAC due to its ability to deliver high concentrations locally, while maintaining low systemic drug levels. Their analysis concluded that patients who received RIAC had a higher rate of partial remission and fewer complications. The studies highlighted show progress within chemotherapy and immunotherapy. There is an urgent need for standardisation of regimens, combination therapy and drug delivery.
Technological advances in radiotherapy (RT) for PDAC were highlighted in a review article by Malla et al. (9). Despite the ability to convert borderline resectable cases to surgical resection, up to a third of patients can die during RT from disease progression. Advances in Stereotactic Body Radiation Therapy (SBRT) and hypofractionation enable the delivery of biologically effective doses with reduced toxicity to surrounding tissues. Specifically, innovation in magnetic resonance-guided on-table adaptive RT is enabling this. A recent phase two trial demonstrated reduced incidence of acute grade 3+ gastrointestinal toxicity at 90 days post treatment. New trials are also being conducted on nanoparticles to enhance RT delivery. Hafnium oxide nanoparticles NBTXR3 are activated by RT to improve radiation-induced abscopal effects. These technologies are likely to improve the effects of neoadjuvant RT for patients with PDAC. Healthcare professionals will have the tools to deliver highly effective doses of RT without the tissue toxicity that currently limits the treatment potential of this therapy.
For patients eligible for surgery, advances in surgical technology are improving outcomes. The uptake of minimally invasive surgery (MIS) for PDAC was analysed by Yan et al. in their meta-analysis of laparoscopic versus open PPPD (10). The 39 studies demonstrated reduced morbidity, length of stay (LOS), blood loss, delayed gastric emptying as well as higher R0 rates in laparoscopic PPPD. The authors importantly highlight that only four randomised controlled studies (RCTs) were included. Two of these were multi-centre and all non-randomised trials were retrospective, showing a need for standardised high-quality surgical trials. The advances of MIS have since been taken further with the advent of robotic surgery. The recently published RCT concerning PDAC has demonstrated safety of the robotic approach for PPPD (11). Novel surgical devices are also prospects for improving patient outcomes. Sheen et al. compared the AEON™ endovascular stapler with traditional devices for laparoscopic distal pancreatectomy in 58 patients (12). Their analysis of using AEON™, characterised by uniform staple lengths and a multi-firing gear, showed a reduction in post-operative day three drain lipase and postoperative pancreatic fistula (POPF) from 65% to 20%. Similar advances have been made in endoscopic ultrasound (EUS). On et al. described the utility of EUS in PDAC in their review. Innovation in the field has enabled EUS-guided interventions such biliary drainage, gastrojejunostomy, coeliac plexus blocks and fiducial placements. Further uptake of interventional EUS is currently limited by a paucity of prospective RCTs. New technologies should be evaluated according to standardised frameworks, such as Idea, Development, Exploration, Assessment and Long-term follow-up, to develop evidence of clinical benefit for patients (13).
One technological area which could improve all aspects of PDAC treatment is Artificial Intelligence (AI). Zhao et al. reviewed the latest achievements of AI in PDAC. Recent advances include AI-based radiomics which can detect PDAC on imaging, and deep learning which can produce precision models for risk prediction and prognostication in PDAC. AI has been used to produce three-dimensional models of tumours, enabling thorough operative planning and improving outcomes such as operative time, blood loss and LOS. One study used artificial neural network models for PDAC prognostication, outperforming corresponding logistic regression models in predicting survival (14).
In summary, technological innovation is transforming the landscape of PDAC treatment. Healthcare professionals are empowered with new tools for detection, therapy delivery, surgery and data analysis in PDAC. Further translational research is needed in multi-biomarker liquid biopsy and RCTs on standardisation of neoadjuvant/adjuvant therapies. Surgical technologies should be evaluated in a robust framework with high quality trials to confer effective and safe treatments for patients with PDAC.
Author contributions
MK: Writing – original draft. AS: Writing – review & editing. SPan: Writing – review & editing. SPat: Writing – review & editing.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Kanno A, Masamune A, Hanada K, Kikuyama M, Kitano M. Advances in early detection of pancreatic cancer. Diagnostics (Basel). (2019) 9. doi: 10.20944/preprints201901.0133.v1
2. Santofimia-Castano P, Iovanna J. Combating pancreatic cancer chemoresistance by triggering multiple cell death pathways. Pancreatology. (2021) 21:522–9. doi: 10.1016/j.pan.2021.01.010
3. McGuigan A, Kelly P, Turkington RC, Jones C, Coleman HG, McCain RS. Pancreatic cancer: A review of clinical diagnosis, epidemiology, treatment and outcomes. World J Gastroenterol. (2018) 24:4846–61. doi: 10.3748/wjg.v24.i43.4846
4. Joliat GR. Latest advances and future challenges in pancreatic surgery. J Clin Med. (2023) 12. doi: 10.3390/jcm12010371
5. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2018) 68:394–424. doi: 10.3322/caac.21492
6. Chen X, Hu X, Liu T. Development of liquid biopsy in detection and screening of pancreatic cancer. Front Oncol. (2024) 14. doi: 10.3389/fonc.2024.1415260
7. Arayici ME, İnal A, Basbinar Y, Olgun N. Evaluation of the diagnostic and prognostic clinical values of circulating tumor DNA and cell-free DNA in pancreatic Malignancies: a comprehensive meta-analysis. Front Oncol. (2024) 14. doi: 10.3389/fonc.2024.1382369
8. Lu C, Zhu Y, Cheng H, Kong W, Zhu L, Wang L, et al. Case report: pathologic complete response to induction therapy in a patient with potentially resectable pancreatic cancer. Front Oncol. (2022) 12. doi: 10.3389/fonc.2022.898119
9. Malla M, Fekrmandi F, Malik N, Hatoum H, George S, Goldberg RM, et al. The evolving role of radiation in pancreatic cancer. Front Oncol. (2023) 12. doi: 10.3389/fonc.2022.1060885
10. Yan Y, Hua Y, Chang C, Zhu X, Sha Y, Wang B. Laparoscopic versus open pancreaticoduodenectomy for pancreatic and periampullary tumor: A meta-analysis of randomized controlled trials and non-randomized comparative studies. Front Oncol. (2023) 12. doi: 10.3389/fonc.2022.1093395
11. Klotz R, Mihaljevic AL, Kulu Y, Sander A, Klose C, Behnisch R, et al. Robotic versus open partial pancreatoduodenectomy (EUROPA): a randomised controlled stage 2b trial. Lancet Reg Health Eur. (2024) 39:100864. doi: 10.1016/j.lanepe.2024.100864
12. Sheen AJ, Bandyopadhyay S, Baltatzis M, Deshpande R, Jamdar S. Carino NdL. Preliminary experience in laparoscopic distal pancreatectomy using the AEON™ endovascular stapler. Front Oncol. (2023) 13. doi: 10.3389/fonc.2023.1146646
13. McCulloch P, Altman DG, Campbell WB, Flum DR, Glasziou P, Marshall JC, et al. No surgical innovation without evaluation: the IDEAL recommendations. Lancet. (2009) 374:1105–12. doi: 10.1016/S0140-6736(09)61116-8
Keywords: pancreas - adenocarcinoma, pancreas, pancrea ticoduodenectomy, technology, innovation
Citation: Kowal M, Smith A, Pandanaboyana S and Pathak S (2024) Editorial: Technological innovations and pancreatic cancer. Front. Oncol. 14:1497367. doi: 10.3389/fonc.2024.1497367
Received: 16 September 2024; Accepted: 17 September 2024;
Published: 07 October 2024.
Edited and Reviewed by:
Liang Qiao, The University of Sydney, AustraliaCopyright © 2024 Kowal, Smith, Pandanaboyana and Pathak. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Mikolaj Kowal, mikolajkowal@doctors.org.uk