Print IconPrint Friendly
Enlarge Text Icon  Minimize Text IconFont Size

Cancer Australia Connections July 2009

Click an article below to read

  • From the CEO

    From the CEO

    As the first half of the year has flown by, we find ourselves at the end of the financial year with many achievements completed along with 2 new projects funded in the 09 Budget: a Lung Cancer program; and a cancer data project that will managed collaboratively with the Australian Institute of Health and Welfare (AIHW). I would like to take this opportunity to thank all of our stakeholders and supporters for their continued contributions to the successful delivery of Cancer Australia’s work.

    Lung cancer is Australia’s single biggest cancer killer with the number of people affected expected to rise over the coming years.  A major factor in the prevalence of lung cancer is smoking and, as such, lung cancer remains the cancer where changing lifestyle can dramatically reduce the number of new cases.  An important factor in treatment of lung cancer is the timely access to the right care at the right time. The new program will include a data component to further understand the way care is currently delivered and help to shape future directions in care, with a special focus on those consumers not referred for more treatment.

    The new Cancer Data to Improve Cancer Survival program is a collaborative project with AIHW to improve the collection or data on cancer care.  It will build on the current level of data already published by investigating the viability of improved staging data especially for metastatic cancer (distant spread).

    In June Dr Ian Roos, Chair, Cancer Voices Victoria joined me to launch the EdCaN suite of resources at the opening of the Cancer Nurses Society Australia (CNSA) conference. This is a great foundation for improved workforce development expanding the role of nurses, allied health workers and better supporting Aboriginal health workers as they encounter cancer.

    Another major achievement is the establishment of 19 new multidisciplinary teams as a result of CanNET and two new jurisdictional cancer plans. This represents a major change in referral patterns resulting in more timely access to the opinions of several health professionals simultaneously especially for people not in metropolitan areas.

    Cancer Australia remains committed to: ongoing education for health professionals; the National Centre for Gynaecological Cancers; targeted cancer research; support for clinical trials; cancer service development; and continued active engagement of consumers.

  • Expression of Interest for Consumer Reviewers

    Expression of Interest for Consumer Reviewers

    Cancer Australia is actively seeking the input of consumers in the assessment of research applications through our Priority-driven Collaborative Cancer Research Scheme (PdCCRS).
    Last year, Cancer Australia called for an Expressions-of-Interest from consumers who were interested in reviewing research grants for Cancer Australia and its funding partners.  In 2008, nine consumers were selected and trained through the Consumer Research Training Workshop hosted by Cancer Council NSW. These trained consumers have positively contributed to the PdCCRS Grant Review Committees and other cancer research assessment panels.
    Due to a strong response to the call for applications for the 2009 Round of the PdCCRS and an increased number of funding partners, Cancer Australia is again calling for Expressions-of-Interest from consumers interested in participating in the review of research applications in the PdCCRS. Cancer Council NSW together with Cancer Australia, will provide training to selected consumers prior to their involvement on Grant Review Committees for 2009 or future rounds of PdCCRS.

    The Expression-of-Interest form and background information is available on the Cancer Australia website at www.canceraustralia.gov.au. Expressions of Interest are now closed and results will be published on the website.

  • Launch of EdCaN

    Launch of EdCaN

    The Cancer Nursing Education (EdCaN) Learning Resources were launched in June 2009 at the Cancer Nurses Society Australia Winter Congress, at Newcastle NSW.

    The Peter MacCallum Cancer Centre, funded by the Australian Government, through Cancer Australia have auspiced the EdCaN project in association with other Australian cancer care institutions, universities and professional colleges and associations.  The Cancer Nurses Society Australia (CNSA) has also been actively involved in the development of the EdCaN learning resources.  The EdCaN team led by Professor Sanchia Aranda (Melbourne University) and Professor Patsy Yates (Queensland University of Technology) has developed a suite of really significant resources for cancer nurses.

    Dr Ian Roos, Chair, Cancer Voices Victoria and Chair of the EdCaN Steering Committee along with Professor David Currow CEO, Cancer Australia, jointly launched the at the opening of the CNSA conference.

    The EdCaN Resources include:
    • A validated National framework for continuing cancer professional development, which will support both the education and continuing professional development of cancer nurses now and into the future;
    • Four cancer education modules centred around 11 case based learning studies which are structured to reflect the patient journey, from finding cancer early to care and support at the end of life;
    • Facilitator’s guides including four cancer specific nursing competency assessment tools; and
    • A portfolio to support each nurse’s continuing professional development.
     
    The EdCaN resources will provide highly flexible and accessible education materials to help: all nurses achieve the core capabilities required in cancer control; specialist cancer nurses benchmark against the specialist cancer nurse competency standards; and educators to facilitate learning for all nurses in cancer control.

    All this is available at: www.cancerlearning.gov.au

  • The National Centre for Gynaecological Cancers Updates

    The National Centre for Gynaecological Cancers Updates

    National Centre for Gynaecological Cancers
    The Centre continues to progress an extensive work program to improve outcomes for women with gynaecological cancers and their care givers. This could not be achieved without the generous support, advice and guidance of the National Centre for Gynaecological Cancers Advisory Group and project working groups. The projects aim to build awareness and improve information and support for women with gynaecological cancers, support the workforce to provide quality gynaecological cancer care and to help build the evidence for optimal treatment of gynaecological cancers.  Key highlights over the last quarter include:

    Working collaboratively with the National Breast and Ovarian Cancer Centre to improve outcomes for women with gynaecological cancers
    The National Centre for Gynaecological Cancers in partnership with the National Breast and Ovarian Cancer Centre (NBOCC) is working to improve the data and reporting of gynaecological cancers.  We have just secured the services of an organisation that will coordinate the pilot testing of the newly developed national specialist minimum data set for gynaecological cancers including ovarian, endometrial and gynaecological cancers.

    Building the evidence in gynaecological cancers
    Dr Mary Ryan has been awarded the first National Institute of Clinical Studies Cancer Australia National Centre for Gynaecological Cancers Clinical Fellowship. Dr Ryan is a clinical nurse consultant at the Royal Hospital for Women in Sydney. She will use her NICS-CA NCGC Fellowship to undertake a two-year implementation project that aims to improve the nutritional status and physical conditioning in women affected by a gynaecological cancer during and after treatment.

    Strengthening the gynaecological cancers workforce
    With the support of the National Centre for Gynaecological Cancers Advisory Group and state and territory health departments, we have commenced the gynaecological cancers workforce project. Comprising three major components, this project will: develop a national service delivery and resource framework for gynaecological cancers; collaborate with states and territories to undertake gynaecological cancer projects within and across state borders to improve outcomes for women with gynaecological cancers; and, procure the services of an organisation to provide national support and coordination of the state and territory projects and build national capacity in gynaecological cancers service delivery.

    Improving information and support for women with gynaecological cancers, their care givers, and families
    The Centre has commissioned GSB Consulting & Communications to adapt or develop and link a suite of information resources on gynecological cancers for consumers and health professionals. This project has been developed with the input and guidance of consumers, the NCGC Advisory Group, the project working group, and organisations which approved inclusion of their materials: Cancer Council NSW, Cancer Council Vic, National Breast and Ovarian Cancer Centre, Gynaecological Cancer Society, National Cancer Institute USA, Cancerbackup UK, and Oncolink USA. The resources will be available soon through the Centre’s website. 

  • Successful 4th CanNET Workshop

    Successful 4th CanNET Workshop

    Cancer Australia has developed the Cancer Service Networks National Demonstration Program, (CanNET) to better link regional and metropolitan cancer services. CanNET involves the Australian, states and Northern Territory governments working collaboratively with consumers of cancer services and health professionals to improve outcomes through better coordination of existing services.

    This project began in 2007 and the implementation phase was funded until June 2009 with the sustainability phase extending to June 2010 in most sites.  The 4th CanNET workshop was held in Melbourne on 11-12 June and provided an opportunity for each of the CanNET to present their achievements, lessons learned and how they have planned to sustain this work into the future.

    The evaluation report is being completed but some of the general outcomes that emerged from the workshop include:

    • CanNET added value and made a substantial contribution across most of the CanNET elements
    • The projects built capacity in regional and rural areas where they operated
    • The Networks identified key enablers and barriers for future network development.

    Effective local governance was a key success factor bringing people together around a common agreed model.  In doing so, the networks supported professionals and services to work better as a team and to take service reform forward.

    The Networks developed high levels of consumer engagement and involvement in service delivery and planning, supporting the jurisdictions to develop substantial knowledge, information and resources on consumer engagement in service delivery and planning.  It became evident that this involvement by consumers increased network members’ recognition of the importance and value of consumer engagement in service delivery and planning in most networks.

    Most Networks developed and disseminated new resources to improve consumer awareness of, and access to, cancer services, including a Directory of Services that at a minimum, provides consumers and general practitioners with up-to-date information about their closest multidisciplinary cancer assessment team (by tumour and postcode).

    An important element of CanNET has been the establishment of new multidisciplinary teams and enhanced support for existing multidisciplinary teams. The impact has been the emergence of 19 new multidisciplinary teams as a result of CanNET.  The multidisciplinary teams include a range of different models; regional and state wide multidisciplinary teams; tumour specific or general multidisciplinary teams and those linking regional/rural clinicians with metropolitan multidisciplinary teams.

    Agreed referral pathways were developed to promote multidisciplinary care and improve consistency in practice.  At least 7 state/territory wide pathways; and 12 network wide pathways have been developed.  Given the considerable time it takes to map pathways and gain agreement, this has been quite an achievement.

    There is still work to do and Cancer Australia has received funding in the 2009-10 Federal Budget, to build on this work to:

    • Develop Networks specifically to address Aboriginal and Torres Strait Islander peoples’ needs;
    • To explore role redesign by testing new and expanded roles;
    • Define and manage minimum case loads; and
    • Further support health professionals through continuing professional development.

    Planning has begun on this work and information about progress will become progressively available on Cancer Australia’s website www.canceraustralia.gov.au as will final outcomes of the CanNET project.

  • Grants awarded in the 2008 round of the Priority-driven Collaborative Cancer Research Scheme (PdCCRS)

    Grants awarded in the 2008 round of the Priority-driven Collaborative Cancer Research Scheme (PdCCRS)

    The Priority-driven Collaborative Cancer Research Scheme (PdCCRS) was established in 2007, to provide funding for cancer research in priority areas and is conducted as an annual, national, cancer research grants scheme. Cancer Australia partners with other funders to provide a nationally coordinated approach to funding of cancer research. In the 2008 PdCCRS round, Cancer Australia partnered with beyondblue: the national depression initiative, Cancer Council Australia, Cure Cancer Australia Foundation, and the National Breast Cancer Foundation. Each funding partner funds research in identified priority areas.

    From a total of 198 applications received from all around Australia in the 2008 PdCCRS, 42 grants were supported, totalling $14.7 million in funding. Cancer Australia is funding or co-funding 41 of these grants. A list of recipients has been posted on Cancer Australia’s website at: http://www.canceraustralia.gov.au/media/28628/successful_2008_pdccrs_grants.pdf.

    Research being funded by these grants is directed towards many of the cancers of highest burden on the Australian population, including: cancers of the lung, breast, prostate, colon, pancreas, and skin. As illustrated in the graphic below, when grouped by main area of research being undertaken, the majority of projects funded by the PdCCRS focus on research that is patient-centred (see below), and seek to complement the traditional pattern of cancer research funding, as shown in the results from Cancer Australia’s National Audit of Cancer Research Projects and Research Programs.

  • 2009 round of the Priority-driven Collaborative Cancer Research Scheme (PdCCRS)

    2009 round of the Priority-driven Collaborative Cancer Research Scheme (PdCCRS)

    Cancer Australia is partnering in the 2009 PdCCRS with beyondblue: the national depression initiative, CanTeen, Cancer Council Australia, the Cure Cancer Australia Foundation, Leukaemia Foundation, Meat and Livestock Australia, the National Breast Cancer Foundation, National Centre for Gynaecological Cancers, Prostate Cancer Foundation of Australia, Radiation Oncology Section Department of Health and Ageing, Starlight Children’s Foundation Australia. Research priorities of Cancer Australia and the funding partners are posted on Cancer Australia’s website at:
    http://www.canceraustralia.gov.au/media/27558/revised_2009_pdccrs_research_priorities.pdf
    The call for applications opened in December 2008 and closed on March 17 2009. Applications are currently under review, and results will be announced towards the end of the year.

  • The National Consumer Advisory Group

    The National Consumer Advisory Group

    The National Consumer Advisory Group, comprising people affected by cancer from across Australia and health professionals, continues to provide support and guidance to Cancer Australia’s work program. Members have been involved in a variety of activities undertaken by Cancer Australia including the development of a consumer value consensus statement that reflects the aspirational needs of consumers affected by cancer; participating in the identification of research priorities for Cancer Australia’s Priority-driven Collaborative Cancer Research Scheme; providing input into the development of Cancer Australia’s website including a consumer portal for cancer clinical trials; and the development of consumer resources.
  • Building Cancer Support Networks Program Rounds Two and Three

    Building Cancer Support Networks Program Rounds Two and Three

    A total of 44 projects have been funded through Building Cancer Support Networks grants program, including 12 projects in Round 2 and 17 projects in Round 3. Round 2 projects are being finalised in June 2009 and project reports are currently being reviewed. There have been some very worthwhile projects and these project reports will be made available on Cancer Australia’s website. Types of projects funded include support groups for women with gynaecological cancer; rural support information resources; technological (IT) support groups for adolescent and young adults with cancer; a national telephone support group for haematological cancers; support for survivors of cancer; information resources for Aboriginal peoples and Torres Strait Islanders; support and resources for people with lung cancer; support for carers of people with cancer and support for people with pancreatic cancer.
  • Improving consumer information about cancer support

    Improving consumer information about cancer support

    Cancer Australia has produced four consumer resources.  The publications have been produced for different target audiences and are available on our website:
    Cancer support groups: A guide to setting up peer facilitated supports and, Cancer support groups: A guide for peer facilitators have been designed to help organisations establish and maintain quality support groups for people living with cancer.
    The Consumer participation guide and the Consumer training and mentoring guide have been developed to support consumers to contribute meaningfully to national cancer policy and programs.
  • Improving cancer care and support through consumer involvement under the Building Cancer Support Networks Program

    Improving cancer care and support through consumer involvement under the Building Cancer Support Networks Program

    Cancer Australia has received $2.6 million in new funding over four years (2009-2013) to further build upon the collaborative work undertaken with state and territory Cancer Councils, the National Aboriginal Community Controlled Organisation and the National Centre for Gynaecological Cancers in Round 3 of the Building Cancer Support Program.  This funding will improve the range and reach of cancer support to people affected by cancer. The new measure will improve and enhance access to community support options for people with cancer and their carers; target new support networks to support and better inform people with identified poorer cancer outcomes, particularly Aboriginal and Torres Strait Islanders and people with cancers that have high early death rates. Cancer Australia will continue to work in collaboration with Cancer Councils, Aboriginal Community Controlled Health Organisations, cancer organisations and key national stakeholders (DoHA) for improved access and sustainability.
© 2007 Cancer Australia ABN 21 075 951 918 All Rights Reserved. Web Design by Next Digital