Early Intervention vs. Standard Palliative Care in Improving End-of-Life Care in Advanced Cancer Patients
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About
RATIONALE: Palliative care may help patients with advanced cancer live more comfortably.
PURPOSE: This randomized clinical trial is studying an early intervention palliative care program to see how well it works compared to a standard care program in improving end-of-life care in patients with advanced lung , gastrointestinal, genitourinary, or breast cancer.
Full description
OBJECTIVES:
- Determine the efficacy of an early intervention palliative care program comprising a phone-based nurse educator and shared medical appointments in improving end-of-life care of patients with advanced lung, gastrointestinal, genitourinary, or breast cancer.
- Compare symptom management, quality of life, and the match between preference of care and the care received in patients treated with an early intervention palliative care program vs a standard care program.
- Compare health care utilization by patients treated with these interventions.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to cancer diagnosis (lung vs breast vs gastrointestinal vs genitourinary) and participating center. Patients are randomized to 1 of 2 intervention arms.
- Arm I (early-intervention palliative care program): Patients complete the Medical Care Questionnaire and receive a computer-generated prescription letter that outlines the problems they have identified; the patient's physician also receives a copy of the letter. Patients receive a series of phone calls weekly for 4 weeks and then at least monthly from a nurse educator. The phone calls address 3 major areas: coordination of palliative care options in the cancer center and the patient's community, including referrals for psychological or spiritual counseling, social work consultation, financial guidance, home health, palliative care or hospice services, and bereavement counseling for the family; problem-solving therapy, focusing on the identification of problems, definition of achievable goals, a plan for reaching those goals, and evaluation of success; and tailored psycho-educational modules from "Charting Your Course", covering end-of-life topics such as symptom management, advanced care planning, communication with the health care team and family members, spirituality, and nutrition. Patients also receive information regarding the purpose and time/location of symptom management, shared medical appointments (SMAs), which they can attend in person or call in to participate via speaker phone. SMAs are 1.5-hour monthly sessions conducted by a physician and a nurse practitioner that can accommodate 10-12 patients and their caregivers. The sessions include a welcome/social period, a question and answer/peer discussion, an interactive educational session, and an opportunity for one-on-one nurse practitioner appointments with a focus on a brief review of the patients' medical treatment plans.
- Arm II (standard palliative care program): Patients receive standard palliative care from their physician/nurse practitioner team and have access to the palliative care nurse at the discretion of the treating physician.
Patients complete Functional Assessment of Chronic Illness Therapy-Palliative Care at baseline and every 3 months thereafter. Patients and caregivers complete surveys measuring their perception of the quality of the patient's cancer care at baseline and at 1 month.
A caregiver or family member completes the After-Death Bereaved Family Member Interview to evaluate the adequacy of patient care at 3 months post-patient death.
PROJECTED ACCRUAL: A total of 450 patients will be accrued for this study.
Enrollment
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Inclusion and exclusion criteria
DISEASE CHARACTERISTICS:
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Diagnosis of 1 of the following advanced cancers:
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Stage IIIB or IV non-small cell lung cancer
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Extensive stage small cell lung cancer
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Stage IV breast cancer
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Poor prognostic indicators (conferring likelihood of ≤ 2 years survival), including, but not limited to, any of the following:
- Visceral crisis
- Lung or liver metastasis
- Estrogen receptor-negative disease
- HER2/neu-positive disease
- Progressive or recurrent disease during or within 2 years of first treatment
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Unresectable stage III or stage IV gastrointestinal cancers
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Stage IV genitourinary cancers
- Prostate cancer must be hormone refractory
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Hormone receptor status:
- Not specified
PATIENT CHARACTERISTICS:
Sex
- Not specified
Menopausal status
- Not specified
Performance status
- Not specified
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
Other
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No dementia or significant confusion (i.e., Mini Mental Exam score < 25)
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No Axis I psychiatric disorders (DSM-IV), including any of the following:
- Schizophrenia
- Bipolar disorder
- Active substance use disorder
PRIOR CONCURRENT THERAPY:
Endocrine therapy
- See Disease Characteristics
Trial design
Primary purpose
Allocation
Interventional model
Masking
329 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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