Evidence map›Paper›PMID 39217601›Full record

Trial reportEuropean heart journal2024

Strain surveillance during chemotherapy to improve cardiovascular outcomes: the SUCCOUR-MRI trial.

Thomas H Marwick, Elizabeth Dewar, Mark Nolan, Mitra Shirazi, Peter Dias, Leah Wright, Ben Fitzgerald, Leighton Kearney, Piyush Srivastava, John Atherton and 7 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in European heart journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Risk-guided cardioprotection in cardio-oncology.Nature cardiovascular research · 2026
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  12. The Current Cardio-Oncology Landscape Across Australia.Current treatment options in oncology · 2026
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  16. Caught in the crossfire: cardiac complications of cancer therapy.The Journal of clinical investigation · 2026
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  17. Integrated Cardio-oncology Service.Cardiac failure review · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Thomas H MarwickImaging Research, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.ORCID 0000-0001-9065-0899
Elizabeth DewarImaging Research, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Mark NolanImaging Research, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Mitra ShiraziDepartment of Cardiology, Royal Adelaide Hospital, Adelaide, SA, Australia.
Peter DiasAdvara Heart Care, Murdoch, WA, Australia.
Leah WrightImaging Research, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Ben FitzgeraldAdvara Heart Care, Brisbane, QLD, Australia.
Leighton KearneyAdvara Heart Care, Melbourne, VIC, Australia.
Piyush SrivastavaAdvara Heart Care, Melbourne, VIC, Australia.
John AthertonUniversity of Queensland Faculty of Medicine, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Kazuaki NegishiCardiology Department, Nepean Hospital, Kingswood, NSW, Australia.
Aaron L SverdlovNewcastle Centre of Excellence in Cardio-Oncology, The University of Newcastle, Hunter Medical Research Institute, Calvary Mater Newcastle, Hunter New England Health, Newcastle, NSW, Australia.
Sudhir WahiPrincess Alexandra Hospital, Brisbane, Australia.
James OttonLiverpool Hospital, Liverpool, NSW, Australia.
Joseph SelvanayagamFlinders University, Adelaide, SA, Australia.
Liza ThomasWestmead Clinical School, University of Sydney and University of New South Wales, Sydney, NSW, Australia.
Paaladinesh ThavendiranathanPeter Munk Cardiac Centre, Toronto General Hospital, Toronto, Ontario, Canada.

Funding

Canada Research Chair in Cardiooncology CRC-2019-00097Canadian Cancer SocietyCanadian Institutes of Health Research's W. David Hargraftinvestigator 2008129National Health and Medical Research Council 1119955National Heart Foundation of Australia Future Leader Fellowship 106025
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe detection of cancer therapy-related cardiac dysfunction (CTRCD) by reduction of left ventricular ejection fraction (LVEF) during chemotherapy usually triggers the initiation of cardioprotective therapy. This study addressed whether the same approach should be applied to patients with worsening of global longitudinal strain (GLS) without attaining thresholds of LVEF.

methodsStrain surveillance during chemotherapy for improving cardiovascular outcomes (SUCCOUR-MRI) was a prospective multicentre randomized controlled trial involving 14 sites. Of 355 patients receiving anthracyclines with normal baseline LVEF, 333 patients (age 59 ± 13 years, 79% women) with at least one other CTRCD risk factor, able to undergo magnetic resonance imaging (MRI), GLS, and three-dimensional echocardiography were tracked over 12 months. A total of 105 patients (age 59 ± 13 years, 75% women, 69% breast cancer) developing GLS-CTRCD (>12% relative reduction of GLS without a change in LVEF) were randomized to cardioprotection with neurohormonal antagonists vs. usual care. The primary endpoint was 12-month change in MRI-LVEF; the secondary endpoint was MRI-LVEF-defined CTRCD.

resultsDuring follow-up, two patients died, and two developed heart failure. Most patients were randomized at 3 months (62%). Median doses of angiotensin inhibition/blockade and beta-blockade were 75% and 50% of respective targets; 21 (43%) had side-effects attributed to cardioprotection. Due to a smaller LVEF change from baseline with cardioprotection than usual care (-2.5 ± 5.4% vs. -5.6 ± 5.9%, P = .009), follow-up LVEF was higher after cardioprotection (59 ± 5% vs. 55 ± 6%, P < .0001). After adjustment for baseline LVEF, the mean (95% confidence interval) difference in the change in LVEF between the two groups was -3.6% (-1.8% to -5.5%, P < .001). After cardioprotection, 1/49 patients developed 12-month LVEF-CTRCD, compared to 6/56 in usual care (P = .075). Global longitudinal strain improved at 3 months post-randomization in the cardioprotection group, with little change with usual care.

conclusionsIn patients with isolated GLS reduction after anthracyclines, cardioprotection is associated with better preservation of 12-month MRI-LVEF compared with usual care.

Indexed as

Stroke VolumeAgedAnthracyclinesAntineoplastic AgentsFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasmsProspective StudiesVentricular Dysfunction, LeftAnthracyclinesAntineoplastic AgentsCancer therapy-related cardiac dysfunctionGlobal longitudinal strainLeft ventricular ejection fraction

Identifiers

PMID39217601
PMCPMC11542702

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.