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Journal article

Defining surrogate endpoints for clinical trials in severe Falciparum malaria.

Abstract:

Objective

To validate surrogate endpoints for mortality in intervention studies in patients with severe malaria

Design

Retrospective evaluation of large intervention studies in severe malaria

Setting, Patients

Three datasets were used: clinical studies in adult patients from Bangladesh, African children enrolled in the ‘AQUAMAT’ study comparing artesunate and quinine, and adult Vietnamese patients in the ‘AQ’ study comparing artemether with quinine.

Measurements

Sequential measurements of plasma lactate and coma score, assessed as absolute change, relative change, slope of the log coma score/lactate time curve and time to clearance/recovery. The prognostic significance of these dynamic measures for mortality were assessed as well as the proportion of treatment effect on mortality explained (PTE) by these surrogate measures.

Main results

Improvements in lactate levels or coma scores, as assessed by any of the explored methods over the first 24 hours of admission, were strongly prognostic for survival in all data sets. The lower adjusted mortality with artemether compared to quinine closely correlated with faster lactate clearance; in hyperlactataemic patient in the AQ study (n=173), the PTE of the relative change in plasma lactate at 8 and 12 hours was 0.81 and 0.75, respectively, indicating good performance. In paediatric patients enrolled in the ‘AQUAMAT’ study with cerebral malaria (n=829), treatment with artesunate as opposed to quinine improved survival, but was not associated with faster coma recovery, whatever measure of improvement was used.

Conclusion

The relative changes in plasma lactate assessed at 8 or 12 hours after admission are valid surrogate endpoints for severe malaria studies on antimalarial drugs or adjuvant treatments aiming at improving the microcirculation. Measures of coma recovery are not valid surrogate endpoints for mortality.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.pone.0169307

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Tropical Medicine
Role:
Author



Publisher:
Public Library of Science
Journal:
PLoS One More from this journal
Volume:
12
Issue:
1
Pages:
e0169307
Publication date:
2017-01-01
Acceptance date:
2016-12-14
DOI:
ISSN:
1932-6203


Language:
English
Keywords:
Pubs id:
pubs:670827
UUID:
uuid:2aa4d588-6d4a-407e-a6e0-22553e247fc7
Local pid:
pubs:670827
Source identifiers:
670827
Deposit date:
2017-01-27
ARK identifier:

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