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Living with and beyond cancer: the GPs role - clinical fact sheet and MCQ

14 October 2026 - Dr Rebecca Chan

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Overview

Improvements in the early detection and treatment of cancer have increased survival rates and the number of Australians living with the long-term consequences of cancer and its treatment.

Up to two-thirds of people who are living with or beyond cancer report ongoing, unmet health care needs across physical, psychological and practical domains, highlighting the importance of coordinated follow-up care.

Although cancer survivorship is generally defined as the period from diagnosis to end of life, in shared care models it most commonly refers to the post-treatment phase, a time during which recurrence is more likely, and individuals may experience long-term and late effects of cancer and its treatments.

Traditionally, follow-up care has been specialist-led and focused on recurrence surveillance. However, growing numbers of Australians affected by cancer and the recognition of broader survivorship needs have driven a shift towards risk-stratified shared-care models that integrate specialist and primary care services. General practice plays a central role in this model, providing accessible, continuous and holistic care.

The role of the GP in post-treatment cancer care

This role is complex and includes:

  • coordination of ongoing medical care and care transitions between specialist and primary care services

  • monitoring for recurrence and facilitation of timely referral back to specialist services as needed

  • management of comorbidities and late treatment effects alongside cancer-specific issues

  • preventive healthcare including immunisation, screening and healthy lifestyle support

  • education about the role of regular exercise as a means of managing treatment-related side effects, supporting long-term health and reducing risk of cancer recurrence

  • supporting psychological wellbeing, including fear of recurrence and cancer-related distress

  • addressing practical concerns like return to work, relationships and financial stress

  • coordinating the involvement of allied health professionals, including exercise physiologists, physiotherapists, psychologists, dietitians and occupational therapists where appropriate, and

  • supporting patient self-management and health literacy

Living well with and beyond cancer requires chronic disease management

People living with and beyond cancer may be at increased risk of:

  • cardiovascular disease, type 2 diabetes and metabolic syndrome due to treatment effects and shared metabolic and lifestyle risk factors

  • osteoporosis, particularly following endocrine therapies such as aromatase inhibitors or androgen deprivation therapy

  • second primary cancers, and

  • long-term residual symptoms related to cancer treatment, eg cancer-related fatigue

Many people will also continue to experience fatigue, pain, neuropathy, cognitive changes, sexual health concerns or reduced functional capacity long after treatment has ended.

Despite their frequent contact with health services, evidence suggests that these patients often experience poorer management of their comorbidities compared to people without a history of cancer. This highlights the importance of ongoing GP involvement to ensure that both cancer-related issues and broader health needs are addressed through comprehensive chronic disease management.

Components of a comprehensive post-treatment review

The mnemonic CAREMAP may help provide a practical framework for structuring consultations and ensuring key domains of care are not overlooked.

Click here to enlarge image

  • Comorbidities: ongoing management of comorbid conditions and chronic disease risk factors

  • Assessment: assessment of new symptoms, functional status, medication changes and adherence

  • Recurrence monitoring: monitoring in accordance with agreed surveillance plans

  • Effects of treatment: identification and management of treatment-related effects such as lymphoedema, menopausal symptoms, bone health, cardiotoxicity, neuropathy, cognitive change

  • Mental wellbeing: screening for psychological distress including fear of recurrence, body image or sexuality concerns

  • Activity, prevention and healthy ageing: review of preventative health measures, including physical activity, weight management, alcohol intake, vaccinations and routine screening

  • Practical issues: discussion of employment, financial wellbeing, relationships and other quality-of-life issues

Practical tips for shared care in post-cancer treatment

  • ensure you have an up-to-date treatment summary from the treating team outlining treatment received, likely late effects, recommended surveillance and red flags for re-referral

  • use My Health Record and other shared communication systems where available to support continuity of care and information sharing

  • clarify roles and responsibilities with both the patient and specialist including who is responsible for surveillance tests, follow-up appointments and ongoing management

  • establish clear pathways for rapid specialist review when recurrence is suspected or complex treatment-related issues arise

  • use longer or structured consultations including chronic care management plans or mental health care plans where appropriate to coordinate care and assist patients accessing allied health services

  • support patient self-management through education about late effects, healthy lifestyle behaviours, symptom monitoring and when to seek medical review

Red flags for referral

  • new or unexplained symptoms suggestive of recurrence or metastatic disease

  • significant, unresolved psychosocial distress

  • uncertainty about surveillance interpretation or next steps

  • complex or emerging late effects outside GP scope (e.g. progressive lymphoedema or suspected treatment-related cardiotoxicity)

Looking ahead

As the number of Australians living with and beyond cancer continues to grow, survivorship care is becoming an increasingly important component of healthcare delivery.

Contemporary Australian frameworks emphasise coordinated, person-centred and risk-stratified care delivered through effective partnerships between specialist and primary care services.  Within these models, GPs are uniquely placed to coordinate care and support people to live well with and beyond cancer.

References 

  1. RACGP. Cancer survivorship shared care. 2024. Available at: https://www.racgp.org.au/FSDEDEV/media/documents/Advocacy/RACGP-Position-statement-Cancer-survivorship-May-2024.pdf.

  2. Emery J. Cancer survivorship – the role of the GP. AFP. 2014; 43(8):521-525.

  3. Vardy JL, Chan RJ, Koczwara B, et al. Clinical Oncology Society of Australia position statement on cancer survivorship care. AJGP. 2019; 48(12):833-836.

  4. Clinical Oncology Society of Australia Model of Survivorship Care Working Group. Model of Survivorship Care: Critical Components of Cancer Survivorship Care in Australia Position Statement. Clinical Oncology Society of Australia. 2016. Available at: https://www.cosa.org.au/common/Uploaded%20files/Position%20Statements/cosa-model-of-survivorship-care-final-11072016.pdf.

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Dr Rebecca Chan
Dr Rebecca Chan

Rebecca is a Sydney-based GP with a special interest in women’s health across the ages, including contraception, antenatal care, and menopause. Over the past ten years, she has worked across various general practices and specialised reproductive and sexual health settings. Alongside her clinical work, she is a medical educator with both the RACGP and Medcast, and has been actively involved in registrar education and training for the past five years.

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