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Not yet recruitingNCT05637567ASAPUpdated Nov 13, 2023

Perioperative Platelet Inhibition With Acetylsalicylic Acid in Patients With Resectable Tumors of the Pancreatic Head

A Phase 2 interventional study of Acetylsalicylic acid and Placebo in Pancreatic Cancer Resectable, sponsored by German Cancer Research Center. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2023-11-13.

Sponsored by German Cancer Research Center · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
170
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This randomized, controlled clinical trial compares the perioperative treatment with acetylsalicylic acid (aspirin) in patients with cancer of the pancreatic head. The main question it aims to answer is: Do patients treated perioperatively with aspirin develop less metastasis after curative resection of pancreatic head tumors?

Participants will be asked to :

  • take a daily aspirin tablet starting 1-4 weeks before surgery until 6 months after surgery
  • participate in regular follow-up visits.
Read the detailed description

With few symptoms, rapid progression and early metastasis pancreatic cancer (pancreatic ductal adenocarcinoma, PDAC) is the third leading cause of cancer death worldwide. In early stages of PDAC, surgical resection followed by adjuvant chemotherapy is the mainstay of treatment. Unfortunately, the majority of patients develop tumor recurrence (most frequently in the liver) despite complete resection and adjuvant treatment. This early postoperative recurrence is a result of preoperatively present, undetected micrometastases, and, most importantly, iatrogenic dissemination of circulating tumor cells (CTCs) by surgical manipulation of the tumor during resection. CTCs can be detected in the majority of PDAC patients and correlate with worse overall survival.

Survival of CTCs in the hostile environment of circulation requires resistance to physical forces (i.e., turbulence, shear stress), but also immune escape mechanisms to avoid clearance by immune cells such as natural killer (NK) cells. CTCs are highly heterogeneous and, by the majority, non-tumorigenic. The number of other nucleated blood cells such as leukocytes greatly exceeds the number of CTCs; in many solid tumors including PDAC, the average number of (detectable) CTCs is less than 10 cells / mL of whole blood. This demonstrates the inefficiency of the metastatic process, which is at least partially a result of early clearance of CTCs after entering the blood stream.

After entering circulation, the first cells that CTCs come in direct contact with are platelets. This leads to activation of platelets and aggregation on the CTCs, which are thus enveloped and protected from the hostile environment in the circulation. This effect is seen in many, but not all CTCs, the underlying molecular mechanisms are currently being investigated. It is conceivable that not only shear forces and turbulence have less influence on CTCs enveloped by platelets, but also that immune cells (e.g. NK cells) in the bloodstream are less likely to detect and eliminate CTCs and therapeutic antibodies have fewer binding sites.

Arguably the most decisive days in the lives of cancer patients are when they undergo surgery for tumor resection. For most solid tumors, surgery is part of all curative treatment regimens. However, the occurrence of distant metastases often brings surgery to its limits, either because not all metastatic lesions are resectable, or due to rapidly recurring metastatic disease after surgery. Many patients develop disseminated disease early after curative resection of an initially non-metastatic tumor. There are several potential reasons behind this phenomenon, most prominently the immunosuppression resulting from major surgery and the iatrogenic dissemination of CTCs during surgery. Surgery-related immunosuppression is addressed by continuous improvement of perioperative medicine such as prehabilitation or early recovery / fast-track programs as well as minimally invasive surgical procedures, whenever possible. However, only few measures have been taken so far to reduce iatrogenic dissemination of tumor cells during PDAC surgery.

During cancer surgery, the tumor is inevitably touched, manipulated or even squeezed as it has to be mobilized from its surroundings while limiting the damage to neighboring structures. This manipulation of the tumor leads to iatrogenic CTC dissemination. The only clinically used measure to reduce tumor cell dissemination during surgery is currently an early ligation of tumor-draining veins prior to manipulation and mobilization of the tumor mass. This method can only be employed in tumor entities that are drained by one or few well-defined veins such as lung cancer or colorectal cancer, in which this method is successfully applied. In other tumors, which are drained by multiple small and/or initially inaccessible vessels (e.g., hepatic tumors) or in which the tumor-draining vein cannot be occluded for prolonged periods of time (e.g., the portal vein draining tumors of the pancreatic head), this "vein first" or "no touch" approach is not applicable. Since especially in pancreatic tumors, hepatic recurrence often occurs after curative resection and inevitably leads to the death of the patient, this represents a major clinical problem.

Approximately 5% of cancer patients are on permanent medication with platelet inhibition (PI), most prominently acetylsalicylic acid (ASA, aspirin) for a cardiac indication. ASA is usually taken orally at a dosage of 100 mg once a day and several studies and meta-analyses have shown that perioperative ASA intake at this standard dosage leads only to a slightly increased risk of bleeding. Therefore, platelet aggregation inhibition with aspirin alone is continued perioperatively nowadays and is classified as safe.

ASA medication leads to increased overall survival in several cancer entities. A meta-analysis of 22 studies evaluating survival of colorectal cancer patients in dependence of ASA treatment revealed a significant survival advantage for patients with continuous ASA treatment in comparison with patients who did not take ASA or terminated ASA intake prior to or at the time point of tumor diagnosis.

So far, despite ample preclinical evidence, only few clinical studies have investigated the effect of ASA treatment on PDAC. Recently published, retrospective data indicates a significantly improved survival after curative resection of PDAC for patients with perioperative low-dose ASA medication, which is directly attributable to a reduced postoperative incidence of distant metastases. A preliminary meta-analysis (incorporating a second study investigating ASA treatment in PDAC) confirms the significantly improved disease-free survival after resection of PDAC in patients under permanent platelet inhibition with ASA. There is also evidence of a reduced incidence of distant metastases under ASA treatment in other tumor entities.

The investigators hypothesize that the reason for the reduced incidence of distant metastases achieved by ASA is the inhibited platelet-mediated protection of CTCs.

In conclusion, perioperative platelet inhibition with ASA may drastically reduce the postoperative incidence of hematogenous metastases with very low toxicity and risk to the patients with PDAC. Despite this favorable benefit-risk ratio, no prospective, randomized-controlled trials investigating this treatment have been conducted. As a result and despite its potential benefits, perioperative ASA treatment in patients undergoing resection of the pancreatic head for malignant indications is currently not generally recommended.

The aim of this multicentric randomized-controlled trial is therefore to investigate the impact of perioperative ASA treatment on the occurrence of hematogenous metastases, survival and perioperative complications in patients undergoing pancreatic head resection (pylorus-preserving pancreaticoduodenectomy / Traverso-Longmire procedure) for PDAC.

02

Conditions studied

  • Pancreatic Cancer Resectable

Keywords

  • pancreatic cancer
  • pancreatic head cancer
  • acetylsalicylic acid
  • aspirin
  • pancreatic head resection
  • liver metastases
  • distant metastases
  • circulating tumor cells
03

In context

Pancreatic Neoplasms

3,235 studies on the registry are indexed under Pancreatic Neoplasms; 899 are open to participants now.

This study's planned enrollment of 170 is above the median of 46 across 2,424 interventional studies indexed under Pancreatic Neoplasms.

Browse Pancreatic Neoplasms studies →

Lead sponsor

German Cancer Research Center is the lead sponsor of 46 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Indication: Patients with (histologically confirmed or clinically suspected) surgically resectable, non-metastatic ductal adenocarcinoma of the pancreatic head
  2. Patients planned for pylorus-preserving partial pancreaticoduodenectomy (PPPD / "ppWhipple" / Traverso-Longmire procedure) (conventional or minimally invasive)
  3. Male and female patients aged 18 to 80 years
  4. Written informed consent of the participating person
  5. ECOG≤2

Exclusion criteria

Exclusion Criteria:

  1. Metastatic disease (distant or peritoneal metastases or lymph node involvement considered distant metastasis (i.e., interaortocaval nodes))
  2. Preoperative use of anticoagulants / thrombolytics (e.g. warfarin, heparin), platelet aggregation inhibitors (e.g. ASA, ticlopidine, clopidogrel), chronic NSAID or metamizole use
  3. Neoadjuvant treatment for locally advanced disease
  4. Presumed necessity of arterial resection (other than gastroduodenal artery)
  5. Advanced liver (INR >1.5 or hepatic encephalopathy) or renal failure (stage IV or higher)
  6. Advanced heart disease (NYHA class ≥ 3)
  7. Known hypersensitivity to ASA or to drugs with a similar chemical structure
  8. History of asthma attacks triggered by salicylates or substances with similar effects
  9. Haemorrhagic diathesis, blood coagulation disorders such as haemophilia or thrombocytopenia
  10. Thrombocytosis > 450,000 / μL
  11. Methotrexate at a dosage of 15 mg or more per week
  12. Participation in competing trials affecting the effects of the investigational medicinal product (IMP) or outcome measures
  13. Addictive or other medical conditions that do not allow the subject to appreciate the nature and scope of the clinical trial and its potential consequences
  14. Pregnant or breast-feeding women
  15. Women of childbearing potential, except women who meet the following criteria:

    • Post-menopausal (12 months natural amenorrhoea or six months amenorrhoea with serum follicle-stimulating hormone (FSH) > 40 U/ml)
    • Postoperative (six weeks after bilateral ovariectomy with or without hysterectomy)
    • Regular and correct use of a contraceptive method with a failure rate \< 1% per year (e.g. implants, depot injections, oral contraceptives, intrauterine devices)
    • Sexual abstinence
    • Vasectomy of partner
  16. Indications that the patient is unlikely to comply with the protocol (e.g. unwillingness to cooperate)
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
170 participants (estimated)

Study arms

  • Experimental
    Treatment Arm

    100 mg acetylsalicylic acid per os once daily, starting 1-4 weeks before surgery until 6 months after surgery

    Drug: Acetylsalicylic acid

  • Placebo comparator
    Control Arm

    Identically looking placebo pill, starting 1-4 weeks before surgery until 6 months after surgery

    Drug: Placebo

Interventions

  • DrugAcetylsalicylic acid

    100 mg per os once daily

  • DrugPlacebo

    Placebo pill per os once daily

06

What researchers measure

Primary outcomes

  1. Hematogenous metastases-free survival

    The primary efficacy endpoint of the study is hematogenous metastases-free survival (HMFS), which is defined as the time from the day of surgery to the date of diagnosis of hematogenous distant metastases (e.g., hepatic or pulmonary metastases) or date of death from any cause, whichever comes first. Peritoneal metastases (peritoneal carcinomatosis) are not regarded hematogenous metastases. The HMFS status is evaluated at regular follow-up examinations for 36 months postoperatively and further recorded during clinical follow-up visits until the end of the trial.

    Time frame: 24 months

Secondary outcomes

  1. Overall survival

    Overall survival (OS) is defined as the time from the day of surgery until death from any cause.

    Time frame: 24 months

  2. Cancer-specific survival

    Cancer-specific survival (CSS) is defined as the time from the day of surgery until death due to the treated cancer or a treatment-related complication.

    Time frame: 24 months

  3. Disease-free survival

    Disease-free survival (DFS) is defined as the time from the day of surgery to the date of diagnosis of tumor recurrence (in any location) or to the date of death from any cause, whichever comes first.

    Time frame: 24 months

  4. Intraoperative blood loss

    Intraoperative blood loss is documented in milliliters during surgery and subsequently analyzed. Intraoperative transfusions of blood or blood components will also be recorded and analyzed.

    Time frame: During surgery

  5. Duration of surgery

    The duration of surgery (first incision to wound closure) is recorded and subsequently analyzed.

    Time frame: During surgery

  6. Perioperative surgical complications

    Surgical complications include postoperative bleeding, anastomotic insufficiencies, pancreatic fistulas, wound infections, fascial dehiscence, delayed gastric emptying (DGE) and gastrointestinal atony.

    Time frame: Until 90 days after surgery

  7. Perioperative medical complications

    Medical complications include pneumonia, myocardial infarction, cardiac decompensation, new onset atrial fibrillation, respiratory insufficiency, renal failure, liver failure and sepsis. Other complications include allergic or intolerance reactions, cerebral infarctions, delirium and pain, prolonging the length of hospital stay.

    Time frame: Until 90 days after surgery

  8. R status

    Will be recorded from pathology report.

    Time frame: during surgery

  9. Number of resected lymph nodes

    Will be recorded from pathology report.

    Time frame: during surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 13, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05637567
Lead sponsor
German Cancer Research Center
Responsible party
Sponsor
First posted
Dec 5, 2022
Start date
Apr 2024 (estimated)
Primary completion
Sep 2028 (estimated)
Completion
Mar 2029 (estimated)
Last update
Nov 13, 2023

Study contacts

Sebastian Schoelch, MD
Contact
s.schoelch@dkfz.de
+49621383 ext. 5152
Johanna Betzler, MD
Contact
johanna.betzler@dkfz.de
+49621383 ext. 5152
Sebastian Schoelch, MD
study chair · German Cancer Research Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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