Early palliative care for patients with advanced cancer: a cluster-randomised controlled trial.

https://arctichealth.org/en/permalink/ahliterature104925
Source
Lancet. 2014 May 17;383(9930):1721-30
Publication Type
Article
Date
May-17-2014
Author
Camilla Zimmermann
Nadia Swami
Monika Krzyzanowska
Breffni Hannon
Natasha Leighl
Amit Oza
Malcolm Moore
Anne Rydall
Gary Rodin
Ian Tannock
Allan Donner
Christopher Lo
Author Affiliation
Division of Medical Oncology and Haematology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Department of Psychiatry, University of Toronto, Toronto, ON, Canada; Department of Psychosocial Oncology and Palliative Care, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Campbell Family Cancer Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada. Electronic address: camilla.zimmermann@uhn.ca.
Source
Lancet. 2014 May 17;383(9930):1721-30
Date
May-17-2014
Language
English
Publication Type
Article
Keywords
Aged
Early Medical Intervention - organization & administration
Female
Follow-Up Studies
Humans
Male
Middle Aged
Neoplasms - psychology - therapy
Ontario
Outpatient Clinics, Hospital - organization & administration
Palliative Care - organization & administration - psychology
Patient satisfaction
Psychometrics
Quality of Life
Single-Blind Method
Treatment Outcome
Abstract
Patients with advanced cancer have reduced quality of life, which tends to worsen towards the end of life. We assessed the effect of early palliative care in patients with advanced cancer on several aspects of quality of life.
The study took place at the Princess Margaret Cancer Centre (Toronto, ON, Canada), between Dec 1, 2006, and Feb 28, 2011. 24 medical oncology clinics were cluster randomised (in a 1:1 ratio, using a computer-generated sequence, stratified by clinic size and tumour site [four lung, eight gastrointestinal, four genitourinary, six breast, two gynaecological]), to consultation and follow-up (at least monthly) by a palliative care team or to standard cancer care. Complete masking of interventions was not possible; however, patients provided written informed consent to participate in their own study group, without being informed of the existence of another group. Eligible patients had advanced cancer, European Cooperative Oncology Group performance status of 0-2, and a clinical prognosis of 6-24 months. Quality of life (Functional Assessment of Chronic Illness Therapy--Spiritual Well-Being [FACIT-Sp] scale and Quality of Life at the End of Life [QUAL-E] scale), symptom severity (Edmonton Symptom Assessment System [ESAS]), satisfaction with care (FAMCARE-P16), and problems with medical interactions (Cancer Rehabilitation Evaluation System Medical Interaction Subscale [CARES-MIS]) were measured at baseline and monthly for 4 months. The primary outcome was change score for FACIT-Sp at 3 months. Secondary endpoints included change score for FACIT-Sp at 4 months and change scores for other scales at 3 and 4 months. This trial is registered with ClinicalTrials.gov, number NCT01248624.
461 patients completed baseline measures (228 intervention, 233 control); 393 completed at least one follow-up assessment. At 3-months, there was a non-significant difference in change score for FACIT-Sp between intervention and control groups (3·56 points [95% CI -0·27 to 7·40], p=0·07), a significant difference in QUAL-E (2·25 [0·01 to 4·49], p=0·05) and FAMCARE-P16 (3·79 [1·74 to 5·85], p=0·0003), and no difference in ESAS (-1·70 [-5·26 to 1·87], p=0·33) or CARES-MIS (-0·66 [-2·25 to 0·94], p=0·40). At 4 months, there were significant differences in change scores for all outcomes except CARES-MIS. All differences favoured the intervention group.
Although the difference in quality of life was non-significant at the primary endpoint, this trial shows promising findings that support early palliative care for patients with advanced cancer.
Canadian Cancer Society, Ontario Ministry of Health and Long Term Care.
Notes
Comment In: Lancet. 2014 May 17;383(9930):1699-70024559580
PubMed ID
24559581 View in PubMed
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