analysis of the systemic (blood) and local (tumor tissue) immune parameters in patients with pancreatic cancer and during conventional therapies could reveal new insights in the interplay of these treatment modalities with the immune system and…
ID
Bron
Aandoening
pancreatic cancer
alvleesklierkanker
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
•To determine the baseline immune signature in pancreatic cancer patients.
Achtergrond van het onderzoek
Patients diagnosed with pancreatic cancer have a poor survival. There is a strong need for new therapeutic approaches. The presence of pancreatic cancer is known to affect the functionality of the immune system and furthermore chemotherapy (CTx) and (chemo)radiotherapy (CRTx) can subvert immunosuppressive mechanisms, or elicit immune responses by immunogenic cell death of cancer cells. In depth analysis of the systemic (blood) and local (tumor tissue) immune parameters in patients with pancreatic cancer and during conventional therapies could reveal new insights in the interplay of these treatment modalities with the immune system and provide a basis/rationale for new (immuno)therapeutic approaches and combination therapies, e.g. including immune checkpoint blockade, adoptive immune therapies, Toll like receptors agonist and interferons in the current standard of care treatments.
Doel van het onderzoek
analysis of the systemic (blood) and local (tumor tissue) immune parameters in patients with pancreatic cancer and during conventional therapies could reveal new insights in the interplay of these treatment modalities with the immune system and provide a basis/rationale for new (immuno)therapeutic approaches and combination therapies.
Onderzoeksopzet
In general we will obtain a baseline sample from every patient (e.g. before surgery or before start of treatment) followed by several samples during their treatment course based on start of therapy and follow-up after each cycle of CTx and/or RTx (maximized at 11 timepoint in total).
Onderzoeksproduct en/of interventie
Blood collection
Algemeen / deelnemers
C.H.J. van Eijck
Surgery department Erasmus MC
Rotterdam 3000 CA
The Netherlands
+31 10 703 3854
c.vaneijck@erasmusmc.nl
Wetenschappers
C.H.J. van Eijck
Surgery department Erasmus MC
Rotterdam 3000 CA
The Netherlands
+31 10 703 3854
c.vaneijck@erasmusmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
•Age ≥ 18 years
•Diagnosed with resectable or borderline resectable pancreatic cancer, locally advanced pancreatic cancer or metastasized pancreatic cancer
•Planned treatment with either of the currently available standard of care treatments for pancreatic cancer (e.g. surgery, gemcitabine, FOLFIRINOX and/or radiotherapy)
•Signed informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
•Unable to draw blood for study purposes
•Serious concomitant systemic disorders that would compromise the safety of the patient or his/her ability to complete the study, at the discretion of the investigator.
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL6173 |
NTR-old | NTR6320 |
CCMO | NL59131.078.16 |
OMON | NL-OMON45549 |