Incidence and timing of common adverse events in lenvatinib-treated patients from the SELECT trial and their association with survival outcomes Journal Article


Authors: Haddad, R. I.; Schlumberger, M.; Wirth, L. J.; Sherman, E. J.; Shah, M. H.; Robinson, B.; Dutcus, C. E.; Teng, A.; Gianoukakis, A. G.; Sherman, S. I.
Article Title: Incidence and timing of common adverse events in lenvatinib-treated patients from the SELECT trial and their association with survival outcomes
Abstract: Purpose: In the study of (E7080) lenvatinib in differentiated cancer of the thyroid, most patients experienced an adverse event. In this report, we examine common lenvatinib-emergent adverse events in this phase three, randomized, double-blind study. Methods: Adverse events were graded per Common Terminology Criteria for Adverse Events v4.0. 392 patients were enrolled (lenvatinib: 261, placebo: 131) and received lenvatinib 24 mg/day or placebo. The main outcome measures were: associations with progression-free survival and overall survival in exploratory univariate and multivariate analyses along with additional variables. Results: The most common any-grade adverse events (any grade; grade 3) in lenvatinib-treated patients included proteinuria (32%; 10%), diarrhea (67%; 9%), fatigue/asthenia/malaise (67%; 10%), rash (23%; 0.4%), and palmar-plantar erythrodysesthesia syndrome (33%; 3%). There were no grade 4 events for these adverse events. They generally occurred early (median time to first onset [weeks]: proteinuria [6.1], diarrhea [12.1], fatigue/asthenia/malaise [3.0], rash [7.3], and palmar-plantar erythrodysesthesia syndrome [5.9]), and were resolved primarily with dose modifications (median time to resolution [weeks]: proteinuria [8.8], diarrhea [18.1], fatigue/asthenia/malaise [16.3], rash [5.9], and palmar-plantar erythrodysesthesia syndrome [20.0]). Discontinuation due to these adverse events occurred in 2 (1%) patients with proteinuria and 4 (2%) with fatigue. Progression-free survival was not associated with any of the adverse events. Eastern Cooperative Oncology Group performance status (P = 0.001), follicular histology (P = 0.002), and diarrhea (P = 0.023) were associated with overall survival in multivariate analyses (median overall survival for patients with diarrhea: not reached; without: 17.1 months). Conclusions: In the study of (E7080) lenvatinib in differentiated cancer of the thyroid, the most common adverse events typically occurred early and were primarily managed with dose modifications. Overall survival was significantly associated with diarrhea. © 2017, The Author(s).
Keywords: adverse event; dose reduction; lenvatinib; dose interruption
Journal Title: Endocrine
Volume: 56
Issue: 1
ISSN: 1355-008X
Publisher: Springer  
Date Published: 2017-01-01
Start Page: 121
End Page: 128
Language: English
DOI: 10.1007/s12020-017-1233-5
PROVIDER: scopus
PUBMED: 28155175
PMCID: PMC5368192
DOI/URL:
Notes: Article -- Export Date: 2 May 2017 -- Source: Scopus
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  1. Eric J Sherman
    344 Sherman