Methadone versus other opioids for refractory malignant bone pain: a pilot randomised controlled study.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
09 Jul 2024
Historique:
received: 07 05 2024
accepted: 01 07 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: epublish

Résumé

Refractory cancer-induced bone pain (CIBP) affects a patient's functional capacity and quality of life, but there is limited evidence to guide opioid choice. We assessed the feasibility, tolerability and possible efficacy of methadone rotation (MR) compared to other opioid rotations (OOR) in this cohort. Adults with CIBP and worst pain intensity ≥ 4/10 and/or opioid toxicity graded ≥ 2 on the Common Terminology Criteria for Adverse Events were randomised 1:1 to methadone or another opioid rotation. Standardised assessment tools were used at pre-defined study time points up to 14 days. Of 51 eligible participants, 38 (74.5%) consented, and 29 (76.3%, MR: 14, OOR: 15) completed the fourteen days follow-up post-opioid rotation. Both groups displayed significant reduction in average (MR: d =  - 1.2, p = 0.003, OOR: d =  - 0.8, p = 0.015) and worst pain (MR: d =  - 0.9, p = 0.042, OOR: d =  - 0.6, p = 0.048) and total pain interference score (MR: d =  - 1.1, p = 0.042, OOR: d =  - 0.7, p = 0.007). Oral morphine equivalent daily dose was reduced significantly in MR compared to the OOR group (d =  - 0.8, p = 0.05). The incidence of opioid-related adverse events following MR was unchanged but lower in the OOR group (d = 0.9, 95% CI 0.1,1.7, p = 0.022). There were no within-group or between-group differences in satisfaction with analgesia at the end of the study. This pilot study demonstrated that MR and OOR in patients with refractory CIBP are feasible, safe and acceptable to patients. Appropriately powered multi-centre randomised controlled studies are needed to confirm the efficacy of MR and OOR in this cohort. ACTRN12621000141842 registered 11 February 2021.

Identifiants

pubmed: 38980427
doi: 10.1007/s00520-024-08706-w
pii: 10.1007/s00520-024-08706-w
doi:

Substances chimiques

Analgesics, Opioid 0
Methadone UC6VBE7V1Z

Types de publication

Journal Article Randomized Controlled Trial Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

495

Informations de copyright

© 2024. The Author(s).

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Auteurs

Merlina Sulistio (M)

Cabrini Health, Melbourne, VIC, 3144, Australia. msulistio@cabrini.com.au.
Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia. msulistio@cabrini.com.au.
School of Medicine, University of Notre Dame Australia, Fremantle, Australia. msulistio@cabrini.com.au.

Alexandra Gorelik (A)

Musculoskeletal Health and Wiser Healthcare Units, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia.

Hoong Jiun Tee (HJ)

Cabrini Health, Melbourne, VIC, 3144, Australia.
Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia.
School of Medicine, University of Notre Dame Australia, Fremantle, Australia.

Robert Wojnar (R)

Cabrini Health, Melbourne, VIC, 3144, Australia.

David Kissane (D)

Cabrini Health, Melbourne, VIC, 3144, Australia.
Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia.
School of Medicine, University of Notre Dame Australia, Fremantle, Australia.

Natasha Michael (N)

Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia.
School of Medicine, University of Notre Dame Australia, Fremantle, Australia.

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