Hugh Green Foundation


Subject: Call for Applications: Part time 0.3-0.5 FTE Gastro-Intestinal (GI) Cancer Clinical Research Fellowship

Subject title: GICI NZ: Call for Applications – Part time 0.3-0.5 FTE GI Cancer Clinical Research Fellowship

The GI Cancer Institute NZ is calling for applications for:

Part time GI Cancer Clinical Fellowship

The GI Cancer Institute NZ offers one part time 0.3-0.5 FTE GI Cancer Clinical Research Fellowship award each year supported by the Hugh Green Foundation. The Fellowship is for the support of outstanding graduates from all relevant health professions, who are able to combine their clinical work with research to improve the quality of life and potential survival for people living with a GI cancer.

The Fellowship is tenable for a period of up to two years. Applications are open to appropriately qualified individuals with New Zealand residency, permanent residency or citizenship, who hold a relevant degree or are in the process of completing their training.

The GI Cancer Clinical Fellowship would be available in (but not limited to) the speciality areas of cancer surgery, radiation oncology, medical oncology, palliative care, cancer genetics, radiology, anatomical pathology, nutrition, psychiatry or public health.

All forms: GICI NZ Call for applications for a GI Cancer Clincal Fellowship 2018 GICI Standard CV Template Please provide all details requested by the 1st March 2018. You will be notified of the outcome of an application by the 1st April 2018.

Dr Janet Rhodes is a surgical registrar trainee who has been awarded $50,000, thanks to the Hugh Green Foundation, to take time out of her clinical work to complete her PhD. Her supervisors are Professor John McCall and Dr Roslyn Kemp who are well known to GICI. Her words below describe the importance of her work.

“Colorectal cancer (CRC) is the second highest cause of cancer death in New Zealand. Some patients require surgery alone, while others need chemotherapy to complete treatment. It is not always clear which patients will require chemotherapy to optimise their chance of survival.
The Immunoscore is a recently developed tool that measures the patient’s immune response to cancer and helps to determine which patients may need additional therapies. My PhD will validate the use of the Immunoscore in New Zealand CRC. I will identify other aspects of the Immunoscore to improve its ability to predict outcomes for the patient”.

Congratulations Janet, we look forward to reading your progress.

GICI is also very pleased to announce an award of $50,000, thanks to the generosity of the Hugh Green Foundation, to Dr Rachel Purcell of the University of Otago.

New Zealand has one of the highest rates of colorectal cancer (CRC) in the world. Dr Purcell and her team will be looking at molecular subtyping and the gut flora in relation to colorectal cancers asking the following two questions.

i) Can molecular subtyping of Colo Rectal Cancer lead to a more personalised approach to treatment and improved outcomes? CRC is a highly heterogeneous disease, with varying clinical outcomes, response to therapy, and morphological features. Currently, no molecular subtyping system, such as the one in place for breast cancer, is in clinical use for CRC in NZ, and consequently more tailored treatments based on molecular profiling are not routinely administered in NZ. Therefore, classification into clinically useful and reproducible subtypes is of utmost importance in order to implement the best available treatment regimen.

ii) How do differences in the gut microbiome contribute to CRC? In addition to validating a classification system that would improve outcome, Dr Purcell seeks to investigate the mechanisms underpinning the development of the spectrum of CRC subtypes. The human colon plays host to a vast and complex microbial community of microorganisms, and gut biome dysfunction is believed to play a role in the development of CRC. Comparison of faecal microbiomes from CRC patients and healthy control has identified particular bacterial species that are enriched in CRC, and analysis of tumour, adenoma, and matched normal tissue from the same patients found that changes in local communities of potentially interacting bacteria, so called ‘meta-communities’, are associated with different disease states.