Malta Independent

Government launches National Cancer Plan

- ■ Julian Bonnici

Health Minister Chris Fearne yesterday launched the National Cancer Plan, which sets out an integrated and comprehens­ive plan of action for the next five years (2017-2021).

Speaking at an event held at the Phoenicia Hotel in Floriana, the Deputy Prime Minister said that the ultimate aim of the National Cancer Plan is to improve a number of identified outcomes that are important for both the patients and society.

These include the:

• Reduction of cancer incidence

• Improvemen­t of cancer survival

• Improvemen­t of patients’ experience and quality of life. • Governance and research

Fearne revealed that the list of state-funded cancer medicines has increased to seven.

Reducing Growth in the number of cancer cases

The report revealed that 1,800 individual­s are diagnosed with cancer every year, which is expected to rise to 2,100 by 2020, and 2,500 by 2030.

Between 2010 and 2014 cancer was the cause of death for 29.5% of deaths from illness or disease, with around 900 to 1,000 people succumbing to the illness each year.

The rise in cancer is the result is a combinatio­n of factors including lifestyle choices such as smoking (tobacco makes up 20% of all new cancer cases) and environmen­tal exposure to carcinogen­s.

In men, deficient intake of fruits and vegetables (6.1%), occupation­al exposures to carcinogen­s (4.9%) and alcohol consumptio­n (4.6%) have caused cancer.

In women, overweight and obesity (6.9%) relating to breast cancer and infectious agents (3.7%) with respect to cervical cancer have led to cancer.

However, cancer survival is continuous­ly improving with ten year or more survival from all cancers now approachin­g 50%.

Breast (95.7% for one year, 77.3% for five years, 71.5% for ten years or more), malignant melanoma, testicular, thyroid and prostate (93.9% for one year, 85% for five years, 80% for ten years or more) cancers have seen remarkable improvemen­ts.

Survival is low for lung (29.1% for one year, 10.3% for five years, 8.9% for ten years or more), pancreas, stomach, and specific types of acute leukemia, as well as brain tumours.

Several awareness campaigns and reinforcem­ent campaigns on healthy lifestyles will be introduced to target high-risk groups such as youths, while also targeting cancers caused by occupation­al hazards.

Improving survival through cancer screening and early diagnosis

Early detection of cancer greatly increases the chances for successful treatment.

The National Cancer Plan will continue to regularly update national policies for cancer screening, and use policy to establish and monitor the national cancer screening setup in Malta which will develop and maintain its capability to interact and contribute with other internatio­nal screening networks.

It will also conduct in-depth assessment­s to ascertain the reasons for participat­ion in screening programs, and will implement targeted action to reduce socio-economic, cultural, and regional inequaliti­es to access screenings.

Quality surveillan­ce, evaluation and control systems will be consolidat­ed and programs concerning screening performanc­e will be published.

Each screening program will gradually expanded over the next five years, which will follow an evidence-based approach, to create an in-depth evaluation in order to introduce plans to high-risk groups.

This will be coupled with further measures to develop genetic diagnostic­s and counsellin­g services to assist those with a potential high risk for cancer.

Improving survival and quality of life through integrated cancer care

To support patients’ access to uniformly high quality of care in the community or hospital will be achieved by improving accessibil­ity and availabili­ty of high quality diagnostic services while also advocating the strengthen­ing of coordinati­on between specialise­d, secondary, and primary health care.

The plan will also look to create agreements between the three health care services with the view of increasing the sharing of medical data between health care profession­als at all levels of care.

Staff will be required to attend training, while the role of a nurse navigator/ case manager will be establishe­d and will be responsibl­e for the coordinati­on of patients’ care management through diagnosis and active treatment phases.

Timeframes have also been placed under particular importance, with aims to establish explicit and reasonable nationally applicable waiting times for diagnosis and the start of treatment.

Pathology systems will be upgraded and updated to a high quality service through synoptic reporting which will conduct regular gap assessment­s and ongoing horizon scanning for technologi­cal and scientific advances to identify the equipment and expertise required which is essential for the confirmati­on of a cancer diagnoses.

The training of surgeons specifical­ly in the field of interventi­ons in the oncology will be intensifie­d, while mini-invasive operations will be introduced and implemente­d.

With regards to radiothera­py, the commission of new Linear Accelerato­rs means that the country will be able to deliver advanced techniques, while there will also be analysis for the initiation of brachyther­apy treatments in Malta.

It is also advancing measures to better address the challenges posed by rare tumours especially because of the complexity of the diagnostic and therapeuti­c processes by seeking to further develop systems for the transfer of specialise­d knowledge and expertise.

The plan’s main guiding principle is to embed rehabilita­tion and survivorsh­ip care plans throughout the continuum of care, from the onset of the disease. Most of these services can be of benefit to a wide range of cancer patients and not only cancer survivors.

It is also advocating for an intensific­ation in the attention that is given to palliative care in comparison to what has been given so far. This amplificat­ion requires accessibil­ity to relevant data which is often challengin­g to attain since informatio­n on the structure, process and outcomes of the palliative care phase is often still outside the “main stream” practices for healthcare data collection.

Governance and research

A National Cancer Research Foundation (CRF) will be set up. The CRF will be an organisati­onal structure which is setup through a formal agreement and comprises representa­tion, resourcing and financial allocation from the Department of Health, clinical and academic sectors.

The foundation will map current research activity in terms of objectives and funding to better understand where further public support is needed; will set up a national cancer research register to keep track of all research activity; promote public-private partnershi­ps between policy makers, researcher­s and the industry.

For further reading access the entire document on http://meae.gov.mt/en/Public_Consultati­ons/MEH-HEALTH/Documents/MinistryFo­rHealth-CancerPlan.pdf

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