Pancreatic Cancer Clinical Trial
Official title:
A Phase 0, Pre-operative, Window-of-opportunity Study to Assess Gene Expression in Patients With Resectable, Locally Advanced, or Metastatic Pancreatic Cancer (NEOPANC-01)
Pancreatic cancer is a lethal disease. The 1-year and 5-year survival rate is approximately
20% and <5% respectively. The treatment options available are limited. Only around 10-20% of
patients present early enough to undergo surgical resection. Furthermore, chemotherapy for
more advanced pancreatic cancer leads to limited survival benefit and can cause significant
side effects. One of the main obstacles to developing new treatments for pancreatic cancer is
the limited understanding of how pancreatic cancer cells change/evolve/adapt following
treatment.
This study is a pilot study to assess whether the investigators can track gene expression
(using a technique called RNA sequencing) in pancreatic cancer cells between two separate
time points. Investigators intend to take a tissue sample (biopsy) of the cancer using
endoscopy ultrasound (EUS) and compare it with samples taken either at the time of surgery in
those patients with resectable disease or follow-up EUS derived biopsies in irresectable
cancers.
The interval between endoscopy and follow-up EUS or surgery will be approximately 2 to 3
weeks and reflects the standard period of time that patients wait from the time point at
which the cancer is deemed to be operable (in the multi-disciplinary team meeting) to the
actual operation.
If the investigators find that the samples (biopsies) taken at EUS and at surgery or
follow-up EUS are comparable they plan to develop future clinical trials of similar design
but with the addition of drug therapy. The investigators will use RNA sequencing to
interrogate the effects of novel cancer drugs on gene expression within the tumour. This will
give them information on how to select patients for therapy, how resistance develops to these
treatments, and allow the investigators to better understand what treatments can be combined
on a rational basis. However, prior to undertaking such studies it is important to understand
how much variability there is in gene expression between sampling at 2 different time points
at which two different techniques are used.
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