The importance of platelets in the pathogenesis of metastasis formation is increasingly recognized. Although evidence from epidemiologic studies suggests positive effects of aspirin on metastasis formation, there is little clinical data on the perioperative use of this drug in pancreatic cancer patients.
From all patients who received curative intent surgery for pancreatic cancer between 2014 and 2016 at our institution, we identified 18 patients that took aspirin at time of admission and continued to throughout the inpatient period. Using propensity score matching, we selected a control group of 64 patients without aspirin intake from our database and assessed the effect of aspirin medication on overall, disease-free, and hematogenous metastasis-free survival intervals as endpoints.
Aspirin intake proved to be independently associated with improved mean overall survival (OS) (46.5 vs. 24.6 months, *p = 0.006), median disease-free survival (DFS) (26 vs. 10.5 months, *p = 0.001) and mean hematogenous metastasis-free survival (HMFS) (41.9 vs. 16.3 months, *p = 0.005). Three-year survival rates were 61.1% in patients with aspirin intake vs. 26.3% in patients without aspirin intake. Multivariate cox regression showed significant independent association of aspirin with all three survival endpoints with hazard ratios of 0.36 (95% CI 0.15–0.86) for OS (*p = 0.021), 0.32 (95% CI 0.16–0.63) for DFS (**p = 0.001), and 0.36 (95% CI 0.16–0.77) for HMFS (*p = 0.009).
Patients in our retrospective, propensity-score matched study showed significantly better overall survival when taking aspirin while undergoing curative surgery for pancreatic cancer. This was mainly due to a prolonged metastasis-free interval following surgery.
In early stages of pancreatic cancer, surgical resection is the most important pillar of therapy. However, a significant proportion of patients will subsequently develop and succumb to distant metastases due to clinically undetectable micrometastasis at the time of surgery.
The “invasion-metastasis cascade” that a localized primary tumor undergoes in order to form metastases, is highly dependent on interactions with healthy cells and components from the surrounding tumor microenvironment . It is highly inefficient concerning the very small proportion of circulating tumor cells (CTCs) that will successfully form overt metastases in distant organs. The vast majority of CTCs dies from sheer stress or elimination by immune cells [2, 3]. Platelets within the circulation collaborate closely with CTCs, protect them from natural killer cells, sustain epithelial–mesenchymal transition (EMT) signals and promote survival through paracrine signals . Thrombocytosis is frequently associated with poor survival and inhibition of platelets can diminish metastasis formation [5, 6]. Thus, the importance of platelets in facilitating metastasis is undisputed .
Aspirin, which is a potent inhibitor of platelet functionality, has been shown to positively affect cancer incidence and cancer-related mortality as reported in epidemiological studies and meta-analysis of randomized controlled trials for cardiovascular prevention [8,9,10,11]. However, only recently randomized controlled trials assessing the effect of aspirin on cancer survival were initiated [12, 13], none of which assess the effect of aspirin in the setting of pancreatic cancer surgery.
Despite the overall positive effect that resection of the primary tumor has on the patient , surgical trauma and physiological changes in the perioperative phase may negatively influence oncological outcome by promoting metastasis formation . In particular, perioperative immunosuppression can lead to a metastasis-permissive state by hampering the main eliminator of circulating cancer cells, the cell-mediated immunity . The perioperative phase represents a short but highly vulnerable phase of the overall disease course in cancer patients. Interference with its pro-metastatic aspects could thus positively affect long-term outcome. We sought to assess this effect by examining patients who continuously took aspirin before, during and after surgery and thus inhibited the main partners in crime of CTCs: platelets.
Study population and propensity score matching
The institutional review board of the University of Munich (study #20-101) approved the study protocol. Patients undergoing pancreatic surgery at our institution between 01/2014 and 11/2016 were registered in a prospectively maintained database. The study period was chosen because in 2014 a change of the department head and standards in pancreatic surgery took place at our institution. We retrospectively identified patients for our study population from this database using a pre-defined study protocol that was designed to address the research question. Inclusion criteria were: (1) confirmed diagnosis of pancreatic ductal adenocarcinoma (PDAC) by pathology, (2) exclusion of distant metastasis at time of surgery, (3) successful resection of primary tumor with curative intent, (4) postoperative survival and/or follow-up of at least 12 weeks, (5) disease-free survival of at least 6 weeks. Patients with diagnosis other than PDAC were excluded as well as patients that suffered from locally advanced disease that underwent neoadjuvant therapy. All PDAC in the database were staged and documented by a pathologist according to the 7th edition AJCC TNM criteria from 2010 . Since we wanted to focus our analysis on the metastases that might be favored by the perioperative period, we excluded patients who developed metastases within the first 6 weeks after resection, as these must have presumably already existed at the time of surgery. We identified 18 patients who were already taking 100 mg aspirin daily at the time of in-patient admission for surgery as part of their regular medication for different indications and who were not paused for this medication at any time during their in-patient stay.
The following variables were extracted from the database as possible confounders: age, sex, American Society of Anesthesiologist (ASA) score, body mass index (BMI), preoperative serum level of carboanhydrate antigen 19-9 (CA19-9), preoperative platelet count, type of resection, intraoperative blood transfusions received, necessity for vascular resection, TNM stage, maximum tumor diameter, examined lymph nodes, lymph node ratio (number of positive nodes divided by resected nodes), residual tumor status (R0 wide, R0 narrow, R1; according to , tumor grading, perineural, vascular, and lymphovascular invasion, and administration of adjuvant therapy.
Follow-up data was acquired by querying the Munich tumor register, by detailed analysis of the electronic patient files for most recent hospital visits and by contacting patients by telephone.
Overall survival (OS) and disease-free survival (DFS) were determined as time interval between day of surgery and day of death (OS)/last follow-up or diagnosis of recurrence (DFS)/last follow-up, respectively. Patients alive or recurrence-free, respectively, at last follow-up visit were censored in the analysis. Patients, in which death from disease was documented but no clear prior date of recurrence diagnosis could be determined, date of recurrence was set to the date of death for DFS. Since our hypothesis foresees an effect of perioperative aspirin specifically on hematogenous metastasis, we analyzed the time interval between surgery and first diagnosis of hematogenous metastasis as “hematogenous metastasis free survival (HMFS)”. Patients that died from other or unknown cause were censored at time of death from cancer specific survival analysis (DFS and HMFS). Patients that died with diagnosis of local recurrence or peritoneal carcinomatosis but without hematogenous metastasis were censored only in HMFS but not DFS.
Propensity score matching
To reduce bias due to confounding variables, propensity score matching (PSM) was performed. PS was estimated as the predicted probability of a patient being on aspirin from a logistic regression model, considering variables that were available prior to surgery and potentially of prognostic value. PSM included T stage, age, sex, ASA score, and tumor diameter. We then formed matched pairs between the 18 patients from the aspirin group and the control group without aspirin using a one-to-four greedy nearest neighbor match without replacement with a caliper width of 0.5 (maximum allowable difference in propensity scores) (SAS software, Cary, NC, USA). The logit of propensity score was used as distance metric and the effective caliper of the matching process was 0.176. Four control patients for each patient of the therapy group were not available under these matching conditions. Thus, the matching process resulted in 18 patients in the therapy group matched to 64 in the control group (effectively 1:3.6 ratio). Good variable balance achieved by the matching process was assured with a treated-to-control variance ratio of the logit of the propensity score of 1.44, which lies between 0.5 and 2 as proposed by Rubin . Only patients matched with PS were included in the time-to-event analyses.
Propensity score matching was performed using SAS, all further analyses were conducted using SPSS© Statistics (version 20, IBM©). Continuous variables were expressed as median with interquartile range (IQR). To detect differences in continuous variables, medians were compared using Mann–Whitney-U test. Potential differences of confounders measured as categorical variables were assessed using cross tabulation and Fisher’s exact-testing. All univariate survival analyses were conducted using Kaplan–Meier estimates and groups compared with log-rank tests. Prior to survival analysis, continuously expressed confounders were categorized by dichotomizing at the median. Two-sided p-values below 0.05 were considered statistically significant. Median, 3- and 5-year survival rates were reported when available. In groups where the number of events was too low to calculate a median survival, mean survival was reported.
Confounding variables that showed influence on the survival estimates (OS, DFS, HMFS) with a p-value of ≤ 0.10 were entered into a multivariate cox regression analysis from which hazard ratios, 95% confidence intervals and two-sided p-values were reported. Parameters with missing data (e.g. adjuvant therapy) were included in the multivariate analysis by adding the category “unknown” to the respective variable to prevent listwise exclusion of cases from multivariate analysis.
Baseline characteristics and tumor stage
Median age of patients was 71 years (IQR: 62–75) and the female to male ratio was 35%:65%. Sixty-seven percent of patients received a pancreaticoduodenectomy, followed by distal pancreatectomy in 22% of patients and total pancreatectomy in 11% of patients. As defined per study protocol and confirmed by histology, all patients suffered from ductal adenocarcinoma of the pancreas. The predominant histopathological features were T3 tumor stage (93% of patients), poor differentiation (G3: 71% of patients) and presence of perineural invasion (Pn1: 87% of patients). Seventy-eight percent of patients showed clear resection margins after surgery (R0). Further patient characteristics are presented in Table 1.
Median follow up for all patients of this study was 20.3 months (IQR: 12.2–31.2 months), with death occurring in 51 patients (62.2%), tumor recurrence of any kind occurring in 64 patients (78%) and development of hematogenous metastasis in 50 patients (61%) during the follow-up period. Median overall survival, disease-free survival, and hematogenous metastasis-free survival were 24.9 months (95% CI 19.0–30.7), 13.6 months (95% CI 10.9–16.3), and 18.3 months (95% CI 13.0–23.7). Three- and five-year survival rates for the whole study population were 34.7% and 23.5%. We were able to confirm routine administration of adjuvant chemotherapy in 59% of all patients with available data on the administration of chemotherapy. Reasons for the omission of chemotherapy were patient choice or poor performance status. In 32% of all patients, we were unable to obtain information on whether or not the recommended adjuvant chemotherapy was administered.
Effect of aspirin on survival parameters
None of the baseline characteristics showed significant differences between groups except for the number of examined lymph nodes (Table 1). In patients with aspirin intake, a median of 33 lymph nodes (IQR: 27–39) was resected and examined compared to a median of 22 resected and examined lymph nodes (IQR: 19–34) in patients without aspirin intake (*p = 0.007). However, the number of examined lymph nodes did not show a significant influence on any of the survival parameters (see Table 2).
Univariate analysis by Kaplan–Meier estimates and log-rank test showed that aspirin intake was associated with longer mean OS compared to no aspirin intake (46.5 vs. 24.6 months, *p = 0.006), longer DFS (26.0 vs. 10.5 months, *p = 0.001) and longer mean HMFS (41.9 vs. 16.3 months, *p = 0.005) (Fig. 1, Table 2).
Other parameters that were significantly associated with longer OS were absent lymphovascular invasion (27.4 vs. 18.9 months, *p = 0.039), absent vascular invasion (27.0 vs. 14.4 months, *p = 0.039) and administration of adjuvant chemotherapy (27.1 vs. 12.4 months, *p = 0.010). Another parameter that showed significant difference in median disease-free survival was absent vascular invasion (16.3 vs. 7.9 months, **p < 0.001). Parameters that were significantly associated with longer hematogenous metastasis free survival were tumor diameter below median (27.0 vs. 16.2 months, *p = 0.032), absent lymphovascular invasion (26.0 vs. 13.9 months, *p = 0.049) and absent vascular invasion (24.9 vs. 9.0 months, **p < 0.001) (Table 2).
All parameters with a p-value of 0.10 or below in univariate analysis were subsequently tested in a multivariate analysis using Cox regression (Table 3). Among all parameters, only aspirin intake was independently associated with better OS (HR 0.36, *p = 0.023), DFS (HR 0.32, **p = 0.001) and HMFS (HR 0.36, *p = 0.010).
Vascular invasion was independently associated with decreased overall survival (HR 3.01, **p = 0.001) and reduced hematogenous metastasis free survival (HR 4.80, **p < 0.001) (Table 3).
Patients suffering from pancreatic cancer have a high risk for recurrence and death despite curative resection with the majority of patients succumbing to diffuse metastatic disease. In fact, 78% of the patients of our curatively resected cohort developed a relapse in the follow-up period of our study and 60.6% died. Our survival results closely resemble those reported in the gemcitabine arm of ESPAC-4, which was the most recent multicentric randomized controlled trial with adjuvant gemcitabine use at the time our patients were treated (OS: 25 vs. 25.5 months, DFS: 13.6 vs. 13.1 months) . Most prognostically relevant baseline characteristics were also comparable to those enrolled in ESPAC-4 [e.g. similar R0 rate (35.4% vs. 40%), maximum tumor diameter (33 mm vs. 30 mm), T3 stage (92.7% vs. 89%)]. Several of the confounders that influenced survival in our study cohort have previously been described to do so in the literature [21, 22].
Aspects related to surgery, such as immunosuppression, release of tumor-supporting factors, and increase of circulating tumor cells (CTCs) by manipulation presumably favor the probability of distant metastases . Platelets have been attributed important roles in increasing the metastatic potential of CTCs by associating with them via tissue factor on the surface of cancer cells . Not only does this screen cancer cells from natural killer cell-mediated killing, it also enables them to benefit from the bioactive molecules abundantly contained in and released by platelets (e.g. TGF-ß and PDGF) [23,24,25]. These molecules cause normal somatic cells, e.g. immune and endothelial cells, to act in favor for the metastatic process . They also support the continuation of EMT pathway activation in CTCs, an important prerequisite for metastatic seeding and otherwise abrogated after losing contact with stromal signals in the primary tumor . Thus, we speculated whether aspirin could counteract negative aspects of the surgical procedure and have a positive impact on patients in this vulnerable phase.
For many decades, aspirin was paused before surgery out of concern for excessive bleeding. This practice has changed only in recent years in our institution out of worry for increased cardiovascular events during surgery, especially owing to the temporarily increased activity of thromboxane A2 after discontinuation of aspirin ("aspirin-withdrawal syndrome") . While the decision to continue aspirin was not based on oncological reasons, it now allows us to assess the clinical outcomes in this patient cohort. In order to be able to detect an effect of perioperative aspirin at all, we considered it important to include only patients in the therapy group who took aspirin permanently and without pausing.
Weighing up potential risks of aspirin, it is known to cause an increase in absolute risk for major bleeding in the general population from about 0.16% to 0.81% over a 15-year period . Most surgical studies, however, show no relevant increase in bleeding risk for patients on aspirin during the perioperative phase and demonstrate a generally high level of safety for the drug . This is consistent with our observations, given that the rate of perioperative blood transfusions was evenly low in both groups of our study.
To our knowledge, there is no published data from randomized phase 3 studies that examine the efficacy of aspirin as cancer therapeutic for pancreatic cancer as an endpoint. However, there are manifold data from experimental, epidemiological, and observational studies, which support the hypothesis of an anti-cancer effect of aspirin . In pre-clinical studies, aspirin has been shown to counteracts cancer stem cell features, desmoplasia and gemcitabine resistance, which was the adjuvant chemotherapy used in in our patient cohort [31, 32]. Furthermore, aspirin reduced Foxp3+ regulatory T cells and prolonged survival in a mouse model and showed effects on Cox-2 expressed in cancer cells, which is involved in carcinogenic pathways (i.e. RAS and NF-κB) .
Metaanalyses of large cohort studies have linked regular aspirin intake with a reduced incidence of various cancers, including colorectal, gastric and prostate cancer ; while research into pancreatic cancer has yielded inconclusive results [34, 35]. Additionally, randomised controlled trials in cardiovascular disease suggest that aspirin may lead to a marked reduction in the mortality associated with several cancer entities. This may be due to a (50%) overall reduction in the occurence of metastases. Further, in patients who primarily develop non-metastatic adenocarcinoma, aspirin reducedthe risk of susequent metastasis formation by approximately 70% . Patients from our study that continuously took aspirin showed significantly longer disease-free and hematogenous metastasis-free intervals (Table 3), which resulted in improved overall survival.
Due to the non-randomized nature and the small sample size of our study, it certainly does not prove that the observed survival benefit is in fact caused by aspirin use. Instead, if aspirin indeed proves to be effective against pancreatic cancer, long-term administration of aspirin could just as well explain the survival benefit observed in our study population by providing continuous protection against the formation of metastases from CTCs prior to surgery or residual tumor cells after surgery. It is however plausible from the suspected mechanism of action and cancer-favoring risks of the surgical procedure, that aspirin intake might be of particular importance in the perioperative setting. Only a prospective randomized controlled trial where patients in the therapy arm are started on aspirin as soon as the diagnosis of pancreatic cancer is suspected, and the medication is continued along with adjuvant chemotherapy until the end of the study could provide answers hereto. In some tumor entities (e.g. colorectal carcinoma) aspirin may exert beneficial effects only after several years of administration, which may reflect the halting effect of aspirin on carcinogenesis, wherease recent studies could demonstrate that aspirin might also provide shortterm benefits by inhibition of metastasis formation [10, 36, 37].
However, despite these broad indications for the efficacy of aspirin in pancreatic cancer or even cancer in general and despite the drug being used safely for many decades in millions of patients, clinical data on the efficacy against cancer is surprisingly sparse.
Our propensity score matched study demonstrates that patients undergoing curative resection of pancreatic adenocarcinoma with continuous perioperative aspirin intake show significantly better survival endpoints than patients without aspirin intake. Taken together with pre-existing evidence, there is sufficient indication of efficacy to justify testing this hypothesis in a prospective randomized study.
Availability of data and materials
The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
American Society of Anesthesiologist
Body mass index
Carboanhydrate antigen 19-9
Circulating tumor cells
Hematogenous metastasis-free survival
Pancreatic ductal adenocarcinoma
Propensity score matching
Fidler IJ. The pathogenesis of cancer metastasis: the “seed and soil” hypothesis revisited. Nat Rev Cancer. 2003;3(6):453–8.
Gupta GP, Massague J. Cancer metastasis: building a framework. Cell. 2006;127(4):679–95.
Headley MB, Bins A, Nip A, Roberts EW, Looney MR, Gerard A, et al. Visualization of immediate immune responses to pioneer metastatic cells in the lung. Nature. 2016;531(7595):513–7.
Labelle M, Hynes RO. The initial hours of metastasis: the importance of cooperative host-tumor cell interactions during hematogenous dissemination. Cancer Discov. 2012;2(12):1091–9.
Gay LJ, Felding-Habermann B. Contribution of platelets to tumour metastasis. Nat Rev Cancer. 2011;11(2):123–34.
Gasic GJ, Gasic TB, Stewart CC. Antimetastatic effects associated with platelet reduction. Proc Natl Acad Sci USA. 1968;61(1):46–52.
Bambace NM, Holmes CE. The platelet contribution to cancer progression. J Thromb Haemost. 2011;9(2):237–49.
Chan AT, Ogino S, Fuchs CS. Aspirin use and survival after diagnosis of colorectal cancer. JAMA. 2009;302(6):649–58.
Holmes MD, Chen WY, Li L, Hertzmark E, Spiegelman D, Hankinson SE. Aspirin intake and survival after breast cancer. J Clin Oncol. 2010;28(9):1467–72.
Rothwell PM, Wilson M, Price JF, Belch JF, Meade TW, Mehta Z. Effect of daily aspirin on risk of cancer metastasis: a study of incident cancers during randomised controlled trials. Lancet. 2012;379(9826):1591–601.
Rothwell PM, Price JF, Fowkes FG, Zanchetti A, Roncaglioni MC, Tognoni G, et al. Short-term effects of daily aspirin on cancer incidence, mortality, and non-vascular death: analysis of the time course of risks and benefits in 51 randomised controlled trials. Lancet. 2012;379(9826):1602–12.
Ali R, Toh HC, Chia WK, Investigators AT. The utility of Aspirin in Dukes C and High Risk Dukes B Colorectal cancer—the ASCOLT study: study protocol for a randomized controlled trial. Trials. 2011;12:261.
Coyle C, Cafferty FH, Rowley S, MacKenzie M, Berkman L, Gupta S, et al. ADD-ASPIRIN: a phase III, double-blind, placebo controlled, randomised trial assessing the effects of aspirin on disease recurrence and survival after primary therapy in common non-metastatic solid tumours. Contemp Clin Trials. 2016;51:56–64.
Imamura M, Doi R, Imaizumi T, Funakoshi A, Wakasugi H, Sunamura M, et al. A randomized multicenter trial comparing resection and radiochemotherapy for resectable locally invasive pancreatic cancer. Surgery. 2004;136(5):1003–11.
Neeman E, Zmora O, Ben-Eliyahu S. A new approach to reducing postsurgical cancer recurrence: perioperative targeting of catecholamines and prostaglandins. Clin Cancer Res. 2012;18(18):4895–902.
Shakhar G, Ben-Eliyahu S. Potential prophylactic measures against postoperative immunosuppression: could they reduce recurrence rates in oncological patients? Ann Surg Oncol. 2003;10(8):972–92.
Edge SB, American Joint Committee on Cancer. AJCC cancer staging manual. 7th ed. New York: Springer; 2010.
Wittekind C, Compton C, Quirke P, Nagtegaal I, Merkel S, Hermanek P, et al. A uniform residual tumor (R) classification: integration of the R classification and the circumferential margin status. Cancer. 2009;115(15):3483–8.
Rubin DB. Health services and outcomes research methodology. 2001. http://rave.ohiolink.edu/ejournals/journal/249347000.
Neoptolemos JP, Palmer DH, Ghaneh P, Psarelli EE, Valle JW, Halloran CM, et al. Comparison of adjuvant gemcitabine and capecitabine with gemcitabine monotherapy in patients with resected pancreatic cancer (ESPAC-4): a multicentre, open-label, randomised, phase 3 trial. Lancet. 2017;389(10073):1011–24.
Hartwig W, Hackert T, Hinz U, Gluth A, Bergmann F, Strobel O, et al. Pancreatic cancer surgery in the new millennium: better prediction of outcome. Ann Surg. 2011;254(2):311–9.
He C, Zhang Y, Cai Z, Lin X, Li S. Overall survival and cancer-specific survival in patients with surgically resected pancreatic head adenocarcinoma: a competing risk nomogram analysis. J Cancer. 2018;9(17):3156–67.
Palumbo JS, Talmage KE, Massari JV, La Jeunesse CM, Flick MJ, Kombrinck KW, et al. Tumor cell-associated tissue factor and circulating hemostatic factors cooperate to increase metastatic potential through natural killer cell-dependent and-independent mechanisms. Blood. 2007;110(1):133–41.
Palumbo JS, Talmage KE, Massari JV, La Jeunesse CM, Flick MJ, Kombrinck KW, et al. Platelets and fibrin(ogen) increase metastatic potential by impeding natural killer cell-mediated elimination of tumor cells. Blood. 2005;105(1):178–85.
Kopp HG, Placke T, Salih HR. Platelet-derived transforming growth factor-beta down-regulates NKG2D thereby inhibiting natural killer cell antitumor reactivity. Cancer Res. 2009;69(19):7775–83.
Labelle M, Begum S, Hynes RO. Direct signaling between platelets and cancer cells induces an epithelial-mesenchymal-like transition and promotes metastasis. Cancer Cell. 2011;20(5):576–90.
Gerstein NS, Schulman PM, Gerstein WH, Petersen TR, Tawil I. Should more patients continue aspirin therapy perioperatively?: clinical impact of aspirin withdrawal syndrome. Ann Surg. 2012;255(5):811–9.
Whitlock EP, Burda BU, Williams SB, Guirguis-Blake JM, Evans CV. Bleeding risks with aspirin use for primary prevention in adults: a systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2016;164(12):826–35.
Wolf AM, Pucci MJ, Gabale SD, McIntyre CA, Irizarry AM, Kennedy EP, et al. Safety of perioperative aspirin therapy in pancreatic operations. Surgery. 2014;155(1):39–46.
Bosetti C, Rosato V, Gallus S, Cuzick J, La Vecchia C. Aspirin and cancer risk: a quantitative review to 2011. Ann Oncol. 2012;23(6):1403–15.
Zhang Y, Liu L, Fan P, Bauer N, Gladkich J, Ryschich E, et al. Aspirin counteracts cancer stem cell features, desmoplasia and gemcitabine resistance in pancreatic cancer. Oncotarget. 2015;6(12):9999–10015.
Jiang MJ, Dai JJ, Gu DN, Huang Q, Tian L. Aspirin in pancreatic cancer: chemopreventive effects and therapeutic potentials. Biochim Biophys Acta. 2016;1866(2):163–76.
Plassmeier L, Knoop R, Waldmann J, Kesselring R, Buchholz M, Fichtner-Feigl S, et al. Aspirin prolongs survival and reduces the number of Foxp3+ regulatory T cells in a genetically engineered mouse model of pancreatic cancer. Langenbecks Arch Surg. 2013;398(7):989–96.
Zhang YP, Wan YD, Sun YL, Li J, Zhu RT. Aspirin might reduce the incidence of pancreatic cancer: a meta-analysis of observational studies. Sci Rep. 2015;5:15460.
Khalaf N, Yuan C, Hamada T, Cao Y, Babic A, Morales-Oyarvide V, et al. Regular use of aspirin or non-aspirin nonsteroidal anti-inflammatory drugs is not associated with risk of incident pancreatic cancer in two large cohort studies. Gastroenterology. 2018;154(5):1380-90.e5.
Flossmann E, Rothwell PM, British Doctors Aspirin T, The UKTIAAT. Effect of aspirin on long-term risk of colorectal cancer: consistent evidence from randomised and observational studies. Lancet. 2007;369(9573):1603–13.
Rothwell PM, Wilson M, Elwin CE, Norrving B, Algra A, Warlow CP, et al. Long-term effect of aspirin on colorectal cancer incidence and mortality: 20-year follow-up of five randomised trials. Lancet. 2010;376(9754):1741–50.
Open Access funding enabled and organized by Projekt DEAL. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Ethics approval and consent to participate
Study appoved by Ethikkommission der LMU München, Pettenkoferstrasse 8, 80336 München, reference number: 20-101.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Pretzsch, E., D’Haese, J.G., Renz, B. et al. Effect of platelet inhibition with perioperative aspirin on survival in patients undergoing curative resection for pancreatic cancer: a propensity score matched analysis. BMC Surg 21, 98 (2021). https://doi.org/10.1186/s12893-021-01083-9
- Actylsalicylic acid
- Adjuvant aspirin
- Circulating tumor cells
- Pancreatic surgery