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29 Sep 2021

Pancreatic cancer ‘priming’ may make chemotherapy more effective

By putting a stop to the cancer environment’s communication with pancreatic cancer cells, research may improve efficiency of chemotherapy for patients.

A new approach to ‘prime’ the tumour environment may improve how effective chemotherapy is for pancreatic ductal adenocarcinoma, one of the most aggressive forms of pancreatic cancer.

In preclinical models, a team at the Garvan Institute of Medical Research could enhance the tumours’ response to chemotherapy by reducing the stiffness and density of the connective tissue known as the stroma, and reduce cancer spread by up to 50%.

The research has paved the way to a clinical trial that will assess whether the therapy approach will be effective for pancreatic ductal adenocarcinoma patients.

“By making cancer cells more sensitive to chemotherapy, we hope to improve survival rates for pancreatic cancer patients,” says Professor Paul Timpson, Cancer Research Theme Leader at the Garvan Institute and co-senior author of the findings published in Science Advances. “This work is a powerful example of cutting-edge research in the laboratory leading to partnership with industry and potential clinical translation.”

New approach to one of the most lethal cancers

Pancreatic ductal adenocarcinoma is an aggressive form of pancreatic cancer and one of the most lethal cancers worldwide. Despite advances in combination chemotherapy approaches, the 5-year survival rate is less than one in ten, and below 3% if the cancer has already metastasised.

“We wanted to try and improve on chemotherapy using a unique approach – targeting the environment around the tumour to make the cancer more sensitive to treatment,” says Dr Kendelle Murphy, first author of the paper.

The researchers investigated FAK – a molecule produced by pancreatic cancer that increases the stiffness of the stroma and helps cancer cells to grow, mobilise and metastasise. Using state-of-the-art intravital imaging techniques to reveal how live pancreatic cancers in mouse models respond to treatment, the researchers investigated whether blocking FAK using an experimental therapy could ‘prime’ cancer cells to be more readily destroyed by chemotherapy.

“When we administered a treatment that targeted FAK prior to chemotherapy in our experimental models, that’s when we saw the most benefits,” says Dr Murphy.

“By pre-treating the tumours with the FAK inhibitors we were changing the stiffness as well as the amount and the deposition of stromal tissue surrounding the cancer cells. On this softer surface, the cancer cells became stalled, rendering them more sensitive to chemotherapy. Effectively, we were increasing the window of vulnerability of these cancer cells to chemotherapy, reducing both pancreatic cancer growth and spread in our models.”

A way to determine who will benefit most

The researchers also discovered that the levels of another protein in pancreatic cancer cells, called merlin, may help identify which individuals would benefit most from FAK targeting.

“Merlin is a protein that is produced at different levels in pancreatic cancer patients. We found that low levels of merlin in our experimental pancreatic cancer models resulted in our ‘priming’ combination approach targeting FAK being more effective,” says Dr David Herrmann, co-senior author of the study.

“We hope that by determining which tumours produce less merlin, we will be able to identify which patients are likely to benefit most from our new combination approach.”

The findings will be investigated as part of a new clinical trial in collaboration with Melbourne-based Amplia Therapeutics Limited, which is set to begin Phase II clinical trials of its FAK inhibitor AMP945 next year to determine if the approach will be effective in patients.

“It is exciting for Amplia to be able to work with Garvan’s extensive experience in FAK biology, cancer biology and clinical expertise. The results of the pre-clinical studies have provided important insights and validated our decision to progress our FAK inhibitor, AMP945, to Phase II clinical trial in pancreatic cancer patients,” says Amplia CEO and Managing Director, Dr John Lambert.

“The survival rates of pancreatic ductal adenocarcinoma patients are dismal and have been largely unchanged for decades,” adds Professor Timpson. “Our approach is a promising new clinically relevant avenue to improve on current treatments, and potentially make a real difference for patients.”


This research was supported by the National Health and Medical Research Council (NHMRC), the Australian Research Council (ARC), Cancer Council NSW, Cancer Institute NSW, Cancer Australia, Tour de Cure, St Vincent’s Clinic Foundation, Suttons, a Len Ainsworth Fellowship in Pancreatic Cancer Research, a Philip Hemstritch Pancreatic Cancer Fellowship, Baxter Family Scholarships, ACRF Incite Centre funding and Sydney Catalyst. The project was made possible by a grant from PanKind, The Australian Pancreatic Cancer Foundation.

Professor Paul Timpson is a member of the scientific advisory board of Amplia Therapeutics Limited. He is a Conjoint Professor at St Vincent's Clinical School, Faculty of Medicine and Health, UNSW Sydney. Dr David Herrmann is a Conjoint Senior Lecturer at St Vincent's Clinical School, Faculty of Medicine and Health, UNSW Sydney. Dr Kendelle Murphy is a Conjoint Associate Lecturer at St Vincent's Clinical School, Faculty of Medicine and Health, UNSW Sydney.

Media contact:

Dr Viviane Richter

Garvan Institute of Medical Research