Study: Supportive care can improve quality of life for people with metastatic breast cancer
Metastatic breast cancer patients have unique needs for treatment and care. Connecting patients to appropriate support services and palliative care is an area of need in health care. A recent study reported improvement in metastatic breast cancer patient quality of life and wellness with an intervention program called the Supportive, Education and Advocacy (MBC-SEA) program. (8/21/19)
Contents
At a glance | Questions for your doctor |
Findings | In-depth |
Clinical trials | Limitations |
Guidelines | Resources |
STUDY AT A GLANCE
This study is about:
whether a program that provides supportive care to breast cancer patients improves their quality of life and health care experience.
Why is this study important?
Metastatic breast cancer patients are known to have unique care, treatment, symptom management, and emotional support needs. is an area of medicine focused on improving or preserving quality of life for people facing life-threatening illnesses such as cancer. Palliative care specialists address a broad range of issues that can affect quality of life and wellbeing. These include pain and symptom management, emotional distress, and advanced care planning, to name a few. This is the first study to evaluate a supportive care program for metastatic breast cancer patients.
Study findings:
The Metastatic Breast Cancer - Support Education and Advocacy (MBC-SEA) program was developed to connect metastatic breast cancer patients with existing supportive and educational services.
Data on 118 women with metastatic breast cancer were measured before and after the MBC-SEA program was started:
- Patients reported improvements in the following outcomes:
- Fewer or lessened symptoms.
- Decreased anxiety and distress
- Greater overall sense of well-being
- More referrals for social work and palliative care (indicating patients were connected with needed services)
- Clinical trial referrals did not increase.
These results were statistically significant. The researchers concluded that support programs like the MBC-SEA can improve care and quality of life for metastatic breast cancer patients.
What does this mean for me?
There is growing effort to meet the supportive care needs of metastatic cancer patients. If you are experiencing symptoms, side effects, emotional distress or other quality of life issues, ask your doctor for a referral to palliative care specialists.
Posted 8/21/19
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References
Reiser V, Rosenzweig M, Welsh A, et al., "The Support, Education and Advocacy (SEA) program of care for women with metastatic breast cancer: a nurse-led palliative care demonstration program." American Journal of Hospice and Palliative Care Medicine. April 11, 2019. doi: 10.1177/1049909119839696.
Disclosure
FORCE receives funding from industry sponsors, including companies that manufacture cancer drugs, tests and devices. All XRAYS articles are written independently of any sponsor and are reviewed by members of our Scientific Advisory Board prior to publication to assure scientific integrity.
The National Comprehensive Cancer Network (NCCN) Practice Guidelines on Standards of Palliative Care include:
- All cancer patients should be screened for palliative care needs at their initial visit, at appropriate intervals and as clinically indicated.
- Patients/families/caregivers should be informed that palliative care is an integral part of their comprehensive cancer care.
- Palliative care specialists should be readily available to provide consultation or direct care to patients/families/caregivers and/or healthcare professionals who request or require their expertise.
Patients, families or caregivers with any of the following conditions or situations should be referred for palliative care:
- uncontrolled symptoms or pain
- moderate-to-severe distress related to diagnosis or treatment
- additional serious physical, psychiatric or psychosocial conditions
- unresolved concerns or lack of understanding about the course of their disease
- advanced cancers
- evidence of worsening prognosis
- communication barriers
- financial limitations
- family discord
Updated: 06/26/2024
- How do I find a palliative care specialist?
- I’m experiencing the following (e.g. pain, loss of appetite, anxiety, etc.), can a palliative care specialist help me? Does your practice have supportive services available?
- My family member or caregiver is having a difficult time coping with my diagnosis. Can a palliative care expert help them?
- What supportive services would you recommend for me?
The following studies are looking at palliative care for people diagnosed with cancer:
- Coaching for Family Caregivers of People with Advanced Cancer from Rural and Minority Communities. This study provides coaching to urban African Americans and white or African American families with cancer who live in the rural Southeast. Navigators working with a palliative care team provide six health coaching sessions either in person or over the phone to help with managing stress and coping, getting and asking for help, improving caregiving skills and decision-making/advance care planning.
- NCT04733469: EMPOWER 3: Improving Palliative Care Health Literacy and Utilization (EMPOWER 3). This study is designed to test an educational intervention to help patients understand palliative care, use it and feel better emotionally and physically.
- NCT04773639: of a Multi-Modal Palliative Care Intervention. This study evaluates a new approach to palliative care to address advanced care planning and psychosocial needs of patients with metastatic cancer.
- NCT06307535: Study of Meaning-Centered Psychotherapy for Caregivers to People With Cancer. Participants will complete questionnaires and will be assigned to receive psychotherapy for 7 sessions.
- NCT05477784: Cancer Parenting Program for the Enhancement of the Quality of Life of Patients With Advanced Cancer and Their Children (EC-PC). This trial examines the usefulness of two educational programs for parents with cancer who have a 5- to 17-year-old child.
Updated: 06/26/2024