Elsevier

European Journal of Cancer

Volume 163, March 2022, Pages 79-87
European Journal of Cancer

Original Research
Improved pyrexia-related outcomes associated with an adapted pyrexia adverse event management algorithm in patients treated with adjuvant dabrafenib plus trametinib: Primary results of COMBI-APlus

https://doi.org/10.1016/j.ejca.2021.12.015Get rights and content
Under a Creative Commons license
open access

Highlights

  • COMBI-APlus met its primary endpoint of reduction in the composite rate of pyrexia.

  • Pyrexia composite rate = grade 3/4 incidence, hospitalisation, and discontinuation.

  • The adapted pyrexia management algorithm interrupted both drugs for pyrexia.

  • Overall safety and early efficacy in COMBI-APlus were consistent with COMBI-AD.

Abstract

Background

COMBI-AD demonstrated long-term benefit of adjuvant dabrafenib plus trametinib in patients with resected stage III BRAF V600E/K–mutant melanoma; however, 9% of patients permanently discontinued therapy due to pyrexia. COMBI-APlus evaluated whether an adapted pyrexia management algorithm reduces high-grade pyrexia and pyrexia-related adverse outcomes.

Methods

COMBI-APlus is an open-label, phase IIIb trial evaluating an adapted pyrexia management algorithm in patients with high-risk resected stage III BRAF V600E/K–mutant melanoma treated with up to 12 months of adjuvant dabrafenib plus trametinib. Both drugs were interrupted for pyrexia (temperature ≥38°C) or the occurrence of pyrexia syndrome for suspected recurrent pyrexia. Treatment was restarted at the same dose once patients were symptom free for ≥24 h. The primary endpoint was the composite rate of grade 3/4 pyrexia, hospitalisation due to pyrexia, or permanent discontinuation due to pyrexia versus historical COMBI-AD control (20.0%; 95% confidence interval [CI], 16.3%–24.1%).

Results

At data cutoff (5 October 2020), COMBI-APlus met its primary endpoint of significant improvement in the composite rate of pyrexia (8.0% [95% CI, 5.9%–10.6%]), with rates of 3.8% for grade 3/4 pyrexia, 4.3% for hospitalisation due to pyrexia, and 2.4% for discontinuation due to pyrexia. Estimated 12-month relapse-free survival was 91.8% (95% CI, 89.0%–93.9%). The most common adverse events were consistent with those in COMBI-AD, and 14.7% of patients permanently discontinued treatment due to adverse events.

Conclusions

The adapted pyrexia management algorithm appears to reduce the incidence of severe pyrexia outcomes, enables patients to manage pyrexia at home, and helps patients remain on treatment.

Clinical trial registration

NCT03551626.

Keywords

BRAF V600–mutant melanoma
Adjuvant
Pyrexia
BRAF inhibitor
Dabrafenib
MEK inhibitor
Trametinib
Targeted therapy

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