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Blood cancer is the third biggest cause of cancer death across Australia, claiming more lives each year than breast cancer or skin cancer.

Blood cancers cover three types; leukaemia, lymphoma and myeloma, and vary greatly, with each cancer type requiring specific and targeted treatments. Cancer Council SA is proud to fund a range of blood cancer research projects, aiming to find new and better ways to detect and treat the disease. We also invest in a number of support programs to ensure that those diagnosed with blood cancers are supported throughout every stage of their cancer journey.

What your donation will fund

$567,755 needed this financial year to complete this valuable work.

To learn more about the the work you'll be supporting, please view the programs below that are funded in part by the Cancer Council SA Blood Cancer Fund.

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Blood Cancer Information

Cancer Council SA is proud to fund a range of blood cancer research projects, aiming to find new and better ways to detect and treat the disease.

Find out more about these research programs below.


Blood cancer research programs

Dr Kate Vandyke; University of Adelaide

Multiple myeloma (MM) is an incurable haematological cancer that is responsible for an estimated 80,000 deaths each year worldwide. Even with the best available current therapies, almost all MM patients eventually relapse, with only 15 per cent of patients surviving 10 years from diagnosis. Previous studies have identified that those patients that have highly “metastatic” MM tumour cells at diagnosis do particularly poorly, leading to rapid disease progression, relapse after treatment and death.  Identification of the factor(s) involved in the recirculation and dissemination process in MM is therefore key in the development of therapeutic strategies that will prevent overt relapse in these patients.

Through your support, we will investigate why some patients do very poorly after diagnosis (surviving less than two years) and identify tailored treatments for this group. Importantly, our work focuses on the repurposing of existing targeted therapies that have been trialed in other disease settings. This makes translation of the results of these studies to the clinic feasible in the short term, meaning that real improvements in survival outcomes should be rapid for these patients who traditionally have had very poor outcomes.

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Professor Deborah White; SAHMRI

Acute Lymphoblastic Leukaemia (ALL) is the most common childhood cancer and remains the leading cause of non-traumatic death in children. Adolescents and young adults with ALL have poor therapeutic outcomes and most adults will die of their disease.

Genomic analysis has revealed several new, high-risk ALL lesions that may be targetable with rational therapies. This is supported by anecdotal reports of significantly improved outcomes, but to date both druggable target identification and patient access to these therapies is limited. Importantly, patients with high risk genomic lesions are currently not recognised at diagnosis and are only screened for genomic lesions when they relapse or fail to respond to chemotherapy; for many patients this is too late. They then undergo high dose toxic chemotherapy and/or transplantation, both associated with life-long risk of co-morbidities and second malignancy. Newer immune based therapies are emerging, but we currently don’t know which patients will benefit from these approaches.

Through your support we will investigate Precision Medicine, integrating genomics, metagenomics, bioinformatics and functional analyses, to provide diagnostic screening and therapeutic triage models that are readily accessible and importantly, will transform treatment and outcomes for our most vulnerable ALL patients. Our group is ideally placed to bring real change for ALL patients to ensure they receive the right therapeutic approach early, improving the clinical outcomes for patients with ALL, which can then extend to other cancers.

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Professor Hamish Scott; University of South Australia

All disease processes in humans have a genetic component, either inherited or acquired by somatic mutation during cell division. It is important to identify genes and mutations that cause disease, predispose families to diseases, or are acquired during disease progression as these are important diagnostic and prognostic markers. They also provide direct targets and biological pathways for therapeutic intervention.

We are interested in how and why these genetic mutations occur, how these changes cause cancer or cancer predisposition, and ways of better treating and monitoring these diseases. Our model diseases are typically, blood cell diseases, such as leukaemias, and lymphomas. Our work on rare inherited cancers with unmet clinical needs has immediate effect such as genetic diagnoses for family planning or selection of bone marrow donors.

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Professor Tim Hughes; University of Adelaide

Just over a decade ago, Chronic Myeloid Leukaemia (CML) was still considered a death sentence. This research has pioneered the use of tyrosine kinase inhibitors (TKIs) to treat a range of cancers including CML, which was once known as one of the most devastating forms of blood cancer. Through the use of TKIs and research into individualised therapies, we have seen significant breakthroughs, with some CML patients even achieving treatment-free cancer remission. This in itself is a remarkable achievement considering that previously, only one in six CML patients survived eight years after their diagnosis.

Thanks to Cancer Council’s Beat Cancer Project, our team has received ongoing funding to support our work since 2013. We’re currently leading a global trial of a promising new therapy for CML, with results to be released later this year. Funding from the Cancer Council’s Beat Cancer Project has enabled our team to lead this and other research projects in South Australia which will ultimately change lives.

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Dr Dagmara Poprawski; Country Health SA

There are currently no cancer clinical trials offered outside of metropolitan Adelaide, meaning that patients from regional areas are required to travel in order to take part. The benefits of cancer patients participating in clinical trials are well recognised, particularly the ability to increase patient access to a full suite of therapy options including novel therapies.

Through your support, we will be able to look at the best way for patients in the South East to be recruited, treated and attend follow-up visits virtually from Mt Gambier hospital directly to sites like Flinders Medical Centre. This Teletrial model will utilise existing services, along with additional resources funded through this application, to establish regional cancer trial sites in the long term.

Even though we’re at early stages, our hope is that the tele-clinical trial model will improve trial participation rates in non-metropolitan areas and ultimately, improve patient care.

 

Professor Caroline Miller and Professor David Roder; SAHMRI and University of South Australia

The South Australia Clinical Cancer Registry (SACCR) consists of four hospital-based clinical cancer registries and a central coordinating unit. The clinical registries provide information on cancer stage, grade, differentiation, treatments (surgery, radiotherapy, chemotherapy etc.), prognostic indicators, patient outcomes and other key indicators of quality cancer care that are needed to complement population incidence registries.

Data is limited to those who are treated at participating hospitals Flinders Medical Centre, The Queen Elizabeth Hospital, Lyell McEwin Health Service and the Royal Adelaide Hospital. Clinical registries provide clinicians and service planners with appropriate insight into current cancer trends and the impacts of changes to clinical practice and models of care on outcomes. There are over 300 data items potentially collected as defined by the South Australian minimum data set.

With the funding received through Cancer Council’s Beat Cancer Project and other revenues, we will be able to continue collecting South Australian cancer-related data, enabling effective public health interventions and cancer incidence monitoring through sharing this data with clinicians and service planners.

Professor Ross McKinnon; Flinders University

My wife succumbed to breast cancer when aged 40. During the 15 months she lived with cancer, she experienced major drug toxicities and many ineffective drug treatments, many of which could have been avoided with better utilisation of biological markers and a higher level of pharmaceutical care. Her experience motivated me to optimise drug treatments for future generations, ensuring that others don’t have to experience what she went through.

The ongoing support of Cancer Council’s Beat Cancer Project will help us develop better and more effective drugs to treat cancer. We are researching across three main areas: using Indigenous knowledge and Australia’s remarkable marine biodiversity to identify new compounds with therapeutic potential in cancer and related conditions; using sophisticated statistical methods to determine if such biomarkers (biological indicators of disease) will be useful decision tools in cancer therapy; and studying the mechanisms by which cancer drugs are metabolised to determine ways to optimise drug strategies.

My message to donors is that drug discovery is difficult and challenging, but through a continuity of funding, we are getting closer to drug breakthroughs every day.

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Professor David Roder; University of South Australia

The primary aim of our unit is to develop more efficient and cost-effective services, especially related to cancer screening and treatment. With cancer impacting one in two Australians by the time they turn 85, our work is to benefit the whole Australian population, with the funding we receive from Cancer Council SA greatly increasing the reach of our work.

Through your support, our next step is to assist in the implementation of evidence-based health policies and evaluate their effectiveness. This work is ongoing, with a major emphasis on evaluating and improving outcomes of services for Aboriginal people. We are also working on assessing side effects of cancer therapies in order to improve the quality of life for those who survive their cancer diagnosis and looking at service evaluation and policy development for breast and cervical screening and cancer treatment services.

Mr Andrew Stanley; SANT Datalink

South Australia has a range of data sets across health, education and social services. Once linked, data describing the health and experience of many thousands of individuals can be supplied to a researcher in a completely de-identified format. This intelligent linkage process strengthens privacy protection while giving researchers access to true population-based data relevant to many areas of research, including cancer prevalence, detection, treatment and outcomes.

Through your support, SANT DataLink is committed to contributing to a better understanding of cancer prevalence, factors contributing to this and improved treatments and outcomes for the community and individuals.

Dr Nicola Poplawski; CALHN

When a client is referred to the AGU we collect and record family history information. The data is collated in KinTrak and clinical staff use the information to determine which cancer genes will be tested and provide an assessment of personal cancer risk.

If a genetic error is identified in a cancer gene, clinical staff use the information to manage risk notification and predictive genetic testing for current and future generations of the family; ensure relatives who do not have the genetic error avoid unnecessary cancer surveillance and provide relatives who do have the genetic error with gene specific risk management advice that lowers their cancer risk (prevention and risk reduction) and enhances detection of early stage cancer (surveillance).

Where ethically approved, research staff use the information to identify individuals/families who are eligible for recruitment to familial cancer research projects; identify individuals/families who are eligible for research or translational genetic testing and contribute data to local, national and international research initiatives relevant to familial cancer

Through support from Cancer Council’s Beat Cancer Project we will be able to employ a data officer to take over these tasks and also support and contribute to AGU research activity, freeing clinical staff for research activities.

Associate Professor Andrew Roland; Flinders University

The project undertaken through this Mid-Career Research Fellowship will address an important impasse that currently prevents cancer patients from achieving the maximum benefit from the use of a key class of anti-cancer medicines. Observational studies consistently show that the benefit achieved by using the class of anti-cancer drugs called kinase inhibitors (KIs) can be dramatically improved, in cases even doubled, by getting the right dose for each patient. Importantly, however, the evidence that comes from these studies is not strong enough to inform practice, and because of this potential value of ‘precision dosing’ for these drugs continues to go unrealised. I have already engaged, and secured funding from, leading local and international academic and pharmaceutical industry partners and established a novel, readily actionable strategy (‘ADMExosomes’) to track the impact of variability in drug exposure on the effectiveness and tolerability of a drug.

Through this fellowship I will evaluate the capacity of this strategy to efficiently generate practice changing evidence defining the value of precision dosing for KIs. Importantly, I have also already established a framework through engagement with my existing network of clinical, consumer and industry collaborators to translate the findings, where appropriate, into actionable ‘companion diagnostics’ that maximise KI effectiveness and tolerability in real world cancer patients.

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Cancer Council SA’s Behavioural Research Team is based at our offices at Greenhill Road. Through your support, the team conducts monitoring, applied research and evaluation to inform the development of Cancer Council SA’s cancer control programs and services. The Behavioural Research Team works closely with the Cancer Council SA Postdoctoral Fellow (Cancer Support) who is jointly based at the Flinders Centre for Innovation in Cancer. Together with two new postgraduate research students from Flinders University, they are interested in people’s knowledge, attitude, behaviours and the decisions individuals make that may lead to healthy or unhealthy behaviours in the area of cancer control, as well as research into the psychosocial impact of cancer on those directly and indirectly affected by cancer.

Dr Ilaria Stefania Pagani; SAHMRI

Chronic myeloid leukaemia (CML) can be controlled by tyrosine kinase inhibitors (TKIs), but about 20 per cent of patients are resistant to first-line therapy and some of them develop fatal blast crisis. Even when treatment is effective most patients need to take TKIs lifelong. This means that there are now thousands of Australians dependent on TKIs, with resulting side effects and costs. Persistent disease indicates the failure of TKIs to target the CML stem cells. Stem cells have a unique metabolic profile characterised by energy production through the mitochondria. Giving a TKI together with a drug that blocks stem cell metabolism could eradicate persistent cells and contribute to an eventual cure. Mitochondria possess their independent DNA (mtDNA), that is more susceptible to mutations than nuclear DNA.

In a preliminary study we showed for the first time that more mutations in mtDNA are associated to a better outcome in CML patients. MtDNA mutations could affect the function of the mitochondrion, increasing its susceptibility to undergo apoptosis in response to TKI therapy. Therefore, stem cells from good responder patients could rely more on glycolysis for their survival. To the contrary, stem cells from poor responder patients, with intact mitochondria, could rely to a different metabolism, for e.g. being more dependent on mitochondrial respiration. The re-purpose of existing drugs targeting metabolic vulnerabilities represents a significant breakthrough in precision medicine and may lead to a rapid translation into clinical practice.

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Professor Timothy Hughes; The University of Adelaide

Even with our current choice of 5 drugs, around 20 per cent of patients with chronic myeloid leukaemia (CML) respond poorly to standard drug therapy. We plan to develop an algorithm based on the most predictive biological and molecular assays to enable a “precision medicine” approach to CML therapy. This “risk-adapted” approach would direct most patients to the safest and cheapest therapy whereas “high risk” patients would receive more potent therapy or enter a trial of combination therapy.

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Dr Madelé van Dyk; Flinders University

Since the discovery kinase inhibitors (KIs), a class of targeted therapy against terminal cancers, progression free survival and overall survival has greatly improved. However, TKIs undergo complex metabolism via liver enzymes (CYP3A4), which is known for its substantial variability in activity. However, no marker to identify CYP3A4 activity in patients currently exists.

Due to the wide inter-individual variability, KI concentrations have varied up to >10 fold. Despite knowing this, variability between patients are inadequately addressed and a ‘one-size fits all’ prescribing is used. This clinical issue is widely recognised but still we do not account for this variability, resulting in some patients experiencing therapeutic failure or toxicity because the dose is not enough or too much.

Therapeutic drug monitoring (TDM) can address this, measuring drug concentrations and changing the dose until the patient’s concentration is in the ‘target concentration’. Based on my previous work I have shown that with the implementation of TDM, we can prolong progression free survival significantly and thus improve patient quality of life. I have also shown that patient characteristics can be used to account for this inter-individual variability. Therefore, this study will evaluate the capacity and benefit of TDM to optimise KI dosing and determine which patient characteristics can help to predict a better dose so that we can personalise treatment to each individual and maximising treatment and minimising side effects. Since the economic health benefit has never been evaluated, this study will the first to address this by performing a cost-benefit analysis.

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Professor Michael Sorich; Flinders University

The research will develop online tools that will help patients to work through difficult decisions about how and when to use an anti-cancer medicine for the treatment of cancer. It will do so by utilising innovative methods to comprehensively analyse a very large amount of data that has recently become available from both clinical studies of medicines and routine use of the medicines by patients. This analysis will allow high-quality predictions to be made regarding a patient’s specific likelihood of benefits and harms from using an anti-cancer medicine.

This research will help overcome barriers to the communication of key information and empower patients by providing doctors with a toolkit to present the treatment options and their key outcomes to the patient in a manner that is personalised to their specific circumstances and characteristics. By having this personalised information, patients can feel more confident and empowered to make the most appropriate decision for them specifically regarding their treatment and will be better prepared by having more accurate expectations for their treatment outcomes.

Additionally, the research will provide insight into the patient and disease characteristics influencing benefit and harms from treatment. These insights provide opportunities to better understand why medicines sometimes don’t work well for certain individuals and how this may be overcome.

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Dr Stephanie Reuter Lange; University of South Australia

Whilst there have been substantial improvements in the treatment of cancer, it remains that three out of 10 patients will not survive longer than five years, a result of either cancer progression or death from severe treatment-related side effects. Cancer medicines must be administered at a dose that is enough to treat the cancer, but not too much to cause toxic side effects. While this is well known, most cancer treatments are given as a “one-size-fits-all” amount. Given the large variability in response seen with many cancer medicines, this means that for the same dose some patients are likely to be under-treated and others a likely to be over-treated.

The concept of dose individualisation is tailoring the amount of drug administered to each individual patient to maximise tumour response and minimise side effects. This fellowship program will use computer-based modelling methods to identify dose individualisation strategies for best treatment practice. This will be conducted for a range of diverse projects that will illustrate the value in this approach to cancer treatment and provide a framework for determining the best use of new and existing cancer medicines.

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Blood cancer support programs

Cancer Council 13 11 20 is a free, confidential phone and web chat service available to anyone impacted by a bowel cancer diagnosis (including bowel cancer), be it the person diagnosed, their family members, friends or loved ones. Experienced cancer nurses are there to answer cancer questions, provide support, connect people to our many other services, or just listen.

In the last year alone, Cancer Council’s dedicated 13 11 20 nurses supported more than 5,000 South Australians impacted by cancer. Through your support, Cancer Council 13 11 20 will continue to be there for all South Australians impacted by cancer, wherever they are in their cancer journey.

For regional South Australians, having to travel to Adelaide for cancer treatment (including blood cancer) can often compound the challenges associated with their diagnosis. Our Lodges at Flinders and Greenhill provide a friendly place to stay, connecting guests to a network of services including meals and shopping, transport to treatment and on-site social work support to help ease the burden of cancer.

In the last year alone, Cancer Council SA provided 30,425 nights of accommodation to 8,938 South Australians at our Lodges. Thanks to the generous support of the South Australian community, especially our fundraisers in regional areas, we are able to continue to provide this service, which acts as a home away from home for all regional South Australians travelling to Adelaide for cancer treatment.

Cancer Council SA provides free counselling, either over the phone or in person, to anyone impacted by a cancer diagnosis (including blood cancer) and their loved ones. We work with people across all stages of their cancer experience, starting from the initial diagnosis, right throughout their treatment and beyond, ensuring that they receive the best support possible throughout their cancer journey.

Thanks to the generous support of the South Australian community, we were able to offer more than 1,800 free counselling sessions last year to South Australians impacted by cancer. Our professional counsellors can help their clients find new ways to manage stress, set personal goals, develop ways to achieve them, or find ways to talk to family and friends about their concerns.

By giving to the Cancer Council SA Blood Cancer Fund, you’ll be helping to ensure this essential service is available to all who need it.

For some, a cancer diagnosis can cause considerable financial stress. That’s why Cancer Council SA offers one-off financial grants to eligible people to help pay household utilities, easing the financial burden of cancer (including blood cancer).

Through the generous support of South Australians, Cancer Council SA provided more than $81,900 in financial assistance in the last year. Your donation today will help us to continue to provide this service for years to come.

When faced with a cancer diagnosis (such as blood cancer), or ongoing cancer treatment, even small tasks can seem overwhelming. Cancer Council SA’s Practical Support Program assists South Australians impacted by cancer who have limited family support by helping out around the house.

Through the generous support of South Australians, Cancer Council SA provided more than $44,000 worth of practical support in the last year across 665 services including cleaning, gardening, child care support and general household duties. Through your support, we will be able to continue to provide this vital service into the future.