Authors
Maree Azzopardi
Rajesh Thomas
Sanjeevan Muruganandan
David C.L Lam
Luke Garske
Benjamin Kwan
Muhammad Redzwan S Rashid Ali
Phan Nguyen
Elaine Yap
Fiona Horwood
Alexander Ritchie
Michael Bint
Claire Tobin
Ranjan Shrestha
Francesco Piccolo
Christian De Chaneet
Jenette Creaney
Robert Newton, Edith Cowan UniversityFollow
Delia Hendrie
Kevin Murray
Catherine Read
David Feller-Kopman
Nick Maskell
Y C Gary Lee
Document Type
Journal Article
Publisher
BMJ Publishing Group
School
Exercise Medicine Research Institute
RAS ID
22313
Funders
Cancer Council of Western Australia
Sir Charles Gairdner Research Advisory Group
Western Australia Cancer and Palliative Care Network (WACPCN).
NHMRC
New South Wales Dust Disease Board
Institute for Respiratory Health and Cancer Council of Western Australia.
Abstract
Introduction
Malignant pleural effusions (MPEs) can complicate most cancers, causing dyspnoea and impairing quality of life (QoL). Indwelling pleural catheters (IPCs) are a novel management approach allowing ambulatory fluid drainage and are increasingly used as an alternative to pleurodesis. IPC drainage approaches vary greatly between centres. Some advocate aggressive (usually daily) removal of fluid to provide best symptom control and chance of spontaneous pleurodesis. Daily drainages however demand considerably more resources and may increase risks of complications. Others believe that MPE care is palliative and drainage should be performed only when patients become symptomatic (often weekly to monthly). Identifying the best drainage approach will optimise patient care and healthcare resource utilisation.
Methods and analysis
A multicentre, open-label randomised trial. Patients with MPE will be randomised 1:1 to daily or symptom-guided drainage regimes after IPC insertion. Patient allocation to groups will be stratified for the cancer type (mesothelioma vs others), performance status (Eastern Cooperative Oncology Group status 0-1 vs ≥ 2), presence of trapped lung (vs not) and prior pleurodesis (vs not). The primary outcome is the mean daily dyspnoea score, measured by a 100 mm visual analogue scale (VAS) over the first 60 days. Secondary outcomes include benefits on physical activity levels, rate of spontaneous pleurodesis, complications, hospital admission days, healthcare costs and QoL measures. Enrolment of 86 participants will detect a mean difference of VAS score of 14 mm between the treatment arms (5% significance, 90% power) assuming a common between-group SD of 18.9 mm and a 10% lost to follow-up rate.
Ethics and dissemination
The Sir Charles Gairdner Group Human Research Ethics Committee has approved the study (number 2015-043). Results will be published in peer-reviewed journals and presented at scientific meetings.
Trial registration number
ACTRN12615000963527; Pre-results.
DOI
10.1136/bmjopen-2016-011480
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
Comments
Azzopardi, M., Thomas, R., Muruganandan, S., Lam, D. C., Garske, L. A., Kwan, B. C., ... & Lee, Y. G. (2016). Protocol of the Australasian Malignant Pleural Effusion-2 (AMPLE-2) trial: a multicentre randomised study of aggressive versus symptom-guided drainage via indwelling pleural catheters. BMJ open, 6(7), e011480.
https://doi.org/10.1136/bmjopen-2016-011480