The University of Southampton
University of Southampton Institutional Repository

The clinical effectiveness of clarithromycin versus endoscopic sinus surgery for adults with chronic rhinosinusitis with and without nasal polyps (MACRO): a pragmatic, multicentre, three-arm, randomised, placebo-controlled phase 4 trial

The clinical effectiveness of clarithromycin versus endoscopic sinus surgery for adults with chronic rhinosinusitis with and without nasal polyps (MACRO): a pragmatic, multicentre, three-arm, randomised, placebo-controlled phase 4 trial
The clinical effectiveness of clarithromycin versus endoscopic sinus surgery for adults with chronic rhinosinusitis with and without nasal polyps (MACRO): a pragmatic, multicentre, three-arm, randomised, placebo-controlled phase 4 trial

Background: a paucity of evidence regarding use of endoscopic sinus surgery and antibiotics in managing chronic rhinosinusitis has contributed to a five-times variation in endoscopic sinus surgery rates, as well as variation in the use of antibiotics. The main aim of the present trial was to compare the clinical effectiveness of endoscopic sinus surgery or 3 months of clarithromycin treatment alongside intranasal medication in adults with chronic rhinosinusitis with or without nasal polyps.

Methods: in this pragmatic, three-arm, randomised, placebo-controlled phase 4 trial, participants were recruited from 20 secondary and tertiary care sites in the UK. Adults (aged ≥18 years) with chronic rhinosinusitis remaining symptomatic following appropriate medical therapy (intranasal corticosteroids, saline nasal irrigations, and a short course of antibiotics) were randomly assigned (1:1:1) to receive endoscopic sinus surgery (within 6 weeks of randomisation if waiting lists allowed) plus intranasal medication, clarithromycin (250 mg twice a day for 2 weeks then 250 mg once a day for 10 weeks) plus intranasal medication, or placebo plus intranasal medication. Intranasal medication comprised intranasal corticosteroids and saline irrigations. Participants were allocated with an automated, web-based secure randomisation system in permuted blocks of varying size (block sizes of three and six), stratified by the presence of polyps and trial site. Participants and site teams were masked to the clarithromycin and placebo allocations, including for outcome assessment. The primary outcome measure was the total score on the 22-item Sino-Nasal Outcome Test (SNOT-22) quality-of-life questionnaire at 6 months after randomisation, with analysis by intention to treat (ITT; available-case basis). Adverse reactions were assessed in the safety population (clarithromycin and placebo), and serious adverse events in the ITT population (all groups). The trial was registered on the ISRCTN registry, ISRCTN36962030, and EudraCT, 2018-001100-11, and is complete, with optional long-term follow-up ongoing. 

Findings: between Nov 1, 2018, and Oct 13, 2023, 514 participants (181 [35%] female and 333 [65%] male), with chronic rhinosinusitis with nasal polyps (n=410) or chronic rhinosinusitis without nasal polyps (n=104), were recruited and randomly assigned to receive endoscopic sinus surgery (n=171), clarithromycin (n=172), or placebo (n=171), all with intranasal medication. SNOT-22 scores at 6 months after randomisation were significantly lower (at the 98·33% confidence level after Bonferroni adjustment) in the endoscopic sinus surgery group than in the clarithromycin group (adjusted mean difference –18·13 [98·33% CI –24·26 to –11·99], p<0·0001) and placebo group (–20·44 [–26·42 to –14·46], p<0·0001). 6-month SNOT-22 scores did not differ significantly between participants randomly assigned to clarithromycin versus placebo (–3·11 [–8·56 to 2·33], p=0·17). Ten serious adverse events occurred in nine participants (two events in two [1%] of 172 participants allocated to clarithromycin, three events in three [2%] of 171 allocated to placebo, and five events in four [2%] of 171 allocated to endoscopic sinus surgery), none of which were fatal.

Interpretation: the MACRO trial shows that endoscopic sinus surgery has clinical effectiveness in patients with chronic rhinosinusitis, providing significantly improved disease-specific quality of life at 6 months. Conversely, the trial findings do not support routine long-term use of low-dose clarithromycin. Endoscopic sinus surgery should be recommended if intranasal medication alone is unable to achieve symptom control. 

Funding: National Institute for Health and Care Research Programme Grants for Applied Research.

Administration, Intranasal, Adult, Aged, Anti-Bacterial Agents/therapeutic use, Chronic Disease, Clarithromycin/therapeutic use, Endoscopy/methods, Female, Humans, Male, Middle Aged, Nasal Polyps/complications, Quality of Life, Rhinosinusitis/complications, Treatment Outcome
0140-6736
926-939
Philpott, Carl
c4cb2471-a719-4ff7-806e-2c9b9bd2da9f
Beard, David J.
54e2f3ec-569f-4897-a00e-bf8ce11ebf7c
Saeedi, Elnaz
3e70f7b1-3c84-4efb-96fc-2b96185afae1
Cook, Jonathan A.
adfa8785-5a00-4d3b-af1f-b07947a0abec
Jones, Stephen
Clarke, Caroline S.
5fef50f9-8644-4356-8d06-5f0cc5e31a57
Teoh, Lucinda
266e8d0b-fb3c-4a1b-bb59-8afad782edc2
Thomas, Mike
997c78e0-3849-4ce8-b1bc-86ebbdee3953
Little, Paul
1bf2d1f7-200c-47a5-ab16-fe5a8756a777
Vennik, Jane
6ee78166-5a7a-433b-87fc-018771f20b19
Lund, Valerie
b04f5441-1bf2-4a03-b0c6-e90c5520bc59
Schilder, Anne G.M.
4efe172e-cbc9-4d1b-b089-f293f5c626ef
Long, Fei
c8f6b2bc-8767-4bfe-9969-3c72c13d0eaa
Durham, Stephen
ad89a1fd-f621-4f1a-b802-de20273e14a7
Boardman, James
227eade9-53f0-419f-bcb4-82152bb7cfa2
Hopkins, Claire
8ed0a5e3-92a3-4988-9c2b-b0e51a8a044c
MACRO Collaborative
Philpott, Carl
c4cb2471-a719-4ff7-806e-2c9b9bd2da9f
Beard, David J.
54e2f3ec-569f-4897-a00e-bf8ce11ebf7c
Saeedi, Elnaz
3e70f7b1-3c84-4efb-96fc-2b96185afae1
Cook, Jonathan A.
adfa8785-5a00-4d3b-af1f-b07947a0abec
Jones, Stephen
Clarke, Caroline S.
5fef50f9-8644-4356-8d06-5f0cc5e31a57
Teoh, Lucinda
266e8d0b-fb3c-4a1b-bb59-8afad782edc2
Thomas, Mike
997c78e0-3849-4ce8-b1bc-86ebbdee3953
Little, Paul
1bf2d1f7-200c-47a5-ab16-fe5a8756a777
Vennik, Jane
6ee78166-5a7a-433b-87fc-018771f20b19
Lund, Valerie
b04f5441-1bf2-4a03-b0c6-e90c5520bc59
Schilder, Anne G.M.
4efe172e-cbc9-4d1b-b089-f293f5c626ef
Long, Fei
c8f6b2bc-8767-4bfe-9969-3c72c13d0eaa
Durham, Stephen
ad89a1fd-f621-4f1a-b802-de20273e14a7
Boardman, James
227eade9-53f0-419f-bcb4-82152bb7cfa2
Hopkins, Claire
8ed0a5e3-92a3-4988-9c2b-b0e51a8a044c

MACRO Collaborative (2025) The clinical effectiveness of clarithromycin versus endoscopic sinus surgery for adults with chronic rhinosinusitis with and without nasal polyps (MACRO): a pragmatic, multicentre, three-arm, randomised, placebo-controlled phase 4 trial. The Lancet, 406 (10506), 926-939. (doi:10.1016/S0140-6736(25)01248-6).

Record type: Article

Abstract

Background: a paucity of evidence regarding use of endoscopic sinus surgery and antibiotics in managing chronic rhinosinusitis has contributed to a five-times variation in endoscopic sinus surgery rates, as well as variation in the use of antibiotics. The main aim of the present trial was to compare the clinical effectiveness of endoscopic sinus surgery or 3 months of clarithromycin treatment alongside intranasal medication in adults with chronic rhinosinusitis with or without nasal polyps.

Methods: in this pragmatic, three-arm, randomised, placebo-controlled phase 4 trial, participants were recruited from 20 secondary and tertiary care sites in the UK. Adults (aged ≥18 years) with chronic rhinosinusitis remaining symptomatic following appropriate medical therapy (intranasal corticosteroids, saline nasal irrigations, and a short course of antibiotics) were randomly assigned (1:1:1) to receive endoscopic sinus surgery (within 6 weeks of randomisation if waiting lists allowed) plus intranasal medication, clarithromycin (250 mg twice a day for 2 weeks then 250 mg once a day for 10 weeks) plus intranasal medication, or placebo plus intranasal medication. Intranasal medication comprised intranasal corticosteroids and saline irrigations. Participants were allocated with an automated, web-based secure randomisation system in permuted blocks of varying size (block sizes of three and six), stratified by the presence of polyps and trial site. Participants and site teams were masked to the clarithromycin and placebo allocations, including for outcome assessment. The primary outcome measure was the total score on the 22-item Sino-Nasal Outcome Test (SNOT-22) quality-of-life questionnaire at 6 months after randomisation, with analysis by intention to treat (ITT; available-case basis). Adverse reactions were assessed in the safety population (clarithromycin and placebo), and serious adverse events in the ITT population (all groups). The trial was registered on the ISRCTN registry, ISRCTN36962030, and EudraCT, 2018-001100-11, and is complete, with optional long-term follow-up ongoing. 

Findings: between Nov 1, 2018, and Oct 13, 2023, 514 participants (181 [35%] female and 333 [65%] male), with chronic rhinosinusitis with nasal polyps (n=410) or chronic rhinosinusitis without nasal polyps (n=104), were recruited and randomly assigned to receive endoscopic sinus surgery (n=171), clarithromycin (n=172), or placebo (n=171), all with intranasal medication. SNOT-22 scores at 6 months after randomisation were significantly lower (at the 98·33% confidence level after Bonferroni adjustment) in the endoscopic sinus surgery group than in the clarithromycin group (adjusted mean difference –18·13 [98·33% CI –24·26 to –11·99], p<0·0001) and placebo group (–20·44 [–26·42 to –14·46], p<0·0001). 6-month SNOT-22 scores did not differ significantly between participants randomly assigned to clarithromycin versus placebo (–3·11 [–8·56 to 2·33], p=0·17). Ten serious adverse events occurred in nine participants (two events in two [1%] of 172 participants allocated to clarithromycin, three events in three [2%] of 171 allocated to placebo, and five events in four [2%] of 171 allocated to endoscopic sinus surgery), none of which were fatal.

Interpretation: the MACRO trial shows that endoscopic sinus surgery has clinical effectiveness in patients with chronic rhinosinusitis, providing significantly improved disease-specific quality of life at 6 months. Conversely, the trial findings do not support routine long-term use of low-dose clarithromycin. Endoscopic sinus surgery should be recommended if intranasal medication alone is unable to achieve symptom control. 

Funding: National Institute for Health and Care Research Programme Grants for Applied Research.

Text
1-s2.0-S0140673625012486-main - Version of Record
Available under License Creative Commons Attribution.
Download (507kB)

More information

e-pub ahead of print date: 28 August 2025
Published date: 28 August 2025
Keywords: Administration, Intranasal, Adult, Aged, Anti-Bacterial Agents/therapeutic use, Chronic Disease, Clarithromycin/therapeutic use, Endoscopy/methods, Female, Humans, Male, Middle Aged, Nasal Polyps/complications, Quality of Life, Rhinosinusitis/complications, Treatment Outcome

Identifiers

Local EPrints ID: 505905
URI: http://eprints.soton.ac.uk/id/eprint/505905
ISSN: 0140-6736
PURE UUID: fbb5e594-5531-4012-80fb-c7b480c83c26
ORCID for Paul Little: ORCID iD orcid.org/0000-0003-3664-1873
ORCID for Jane Vennik: ORCID iD orcid.org/0000-0003-4602-9805

Catalogue record

Date deposited: 22 Oct 2025 17:03
Last modified: 23 Oct 2025 01:53

Export record

Altmetrics

Contributors

Author: Carl Philpott
Author: David J. Beard
Author: Elnaz Saeedi
Author: Jonathan A. Cook
Author: Stephen Jones
Author: Caroline S. Clarke
Author: Lucinda Teoh
Author: Mike Thomas
Author: Paul Little ORCID iD
Author: Jane Vennik ORCID iD
Author: Valerie Lund
Author: Anne G.M. Schilder
Author: Fei Long
Author: Stephen Durham
Author: James Boardman
Author: Claire Hopkins
Corporate Author: MACRO Collaborative

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×