Randomized Trial of a Palliative Care Intervention to Improve End-of-Life Care Discussions in Patients With Metastatic Breast Cancer

Author:

Greer Joseph A.12,Moy Beverly12,El-Jawahri Areej12,Jackson Vicki A.12,Kamdar Mihir12,Jacobsen Juliet12,Lindvall Charlotta23,Shin Jennifer A.12,Rinaldi Simone12,Carlson Heather A.12,Sousa Angela12,Gallagher Emily R.1,Li Zhigang4,Moran Samantha5,Ruddy Magaret6,Anand Maya V.7,Carp Julia E.8,Temel Jennifer S.12

Affiliation:

1. 1Massachusetts General Hospital,

2. 2Harvard Medical School, and

3. 3Dana-Farber Cancer Institute, Boston, Massachusetts;

4. 4University of Florida, Gainesville, Florida;

5. 5Massachusetts General Hospital Institute of Health Professions, Boston, Massachusetts;

6. 6University of Massachusetts Medical School, Worcester, Massachusetts;

7. 7University of Rochester School of Medicine and Dentistry, Rochester, New York; and

8. 8Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.

Abstract

Background: Studies show that early, integrated palliative care (PC) improves quality of life (QoL) and end-of-life (EoL) care for patients with poor-prognosis cancers. However, the optimal strategy for delivering PC for those with advanced cancers who have longer disease trajectories, such as metastatic breast cancer (MBC), remains unknown. We tested the effect of a PC intervention on the documentation of EoL care discussions, patient-reported outcomes, and hospice utilization in this population. Patients and Methods: Patients with MBC and clinical indicators of poor prognosis (n=120) were randomly assigned to receive an outpatient PC intervention (n=61) or usual care (n=59) between May 2, 2016, and December 26, 2018, at an academic cancer center. The intervention entailed 5 structured PC visits focusing on symptom management, coping, prognostic awareness, decision-making, and EoL planning. The primary outcome was documentation of EoL care discussions in the electronic health record (EHR). Secondary outcomes included patient-report of discussions with clinicians about EoL care, QoL, and mood symptoms at 6, 12, 18, and 24 weeks after baseline and hospice utilization. Results: The rate of EoL care discussions documented in the EHR was higher among intervention patients versus those receiving usual care (67.2% vs 40.7%; P=.006), including a higher completion rate of a Medical Orders for Life-Sustaining Treatment form (39.3% vs 13.6%; P=.002). Intervention patients were also more likely to report discussing their EoL care wishes with their doctor (odds ratio [OR], 3.10; 95% CI, 1.21–7.94; P=.019) and to receive hospice services (OR, 4.03; 95% CI, 1.10–14.73; P=.035) compared with usual care patients. Study groups did not differ in patient-reported QoL or mood symptoms. Conclusions: This PC intervention significantly improved rates of discussion and documentation regarding EoL care and delivery of hospice services among patients with MBC, demonstrating that PC can be tailored to address the supportive care needs of patients with longer disease trajectories. ClinicalTrials.gov identifier: NCT02730858

Publisher

Harborside Press, LLC

Subject

Oncology

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