Use of a Healthcare Claims Database for Post-Marketing Safety Assessments of Eribulin in Japan: A Comparative Assessment with a Prospective Post-Marketing Surveillance Study.


Journal

Drugs - real world outcomes
ISSN: 2199-1154
Titre abrégé: Drugs Real World Outcomes
Pays: Switzerland
ID NLM: 101658456

Informations de publication

Date de publication:
Mar 2019
Historique:
pubmed: 9 3 2019
medline: 9 3 2019
entrez: 9 3 2019
Statut: ppublish

Résumé

To understand the extent to which a large-scale healthcare claims database (DB) captures the safety profile of eribulin mesylate (Halaven We descriptively summarized patient characteristics and AEs of 551 and 951 patients retrieved from DB and PMS, respectively, during 2011‒2013. Using 2814 patient data from the DB during 2011‒2016, the drug use and AE incidence over time were assessed. In both datasets, 99.8% were females, and the mean age was 57.8 ± 10.7 years. The mean number of eribulin administration was 11.1 ± 10.9 and 10.1 ± 7.8 in DB and PMS, respectively. Although, overall, the difference in AE incidence between the two datasets was moderate, gaps were larger for nausea (DB: 73.32% vs. PMS: 15.77%), neutropenia (20.87% vs. 66.67%), stomatitis (37.39% vs. 10.94%), and alopecia (0.36% vs. 12.09%). During 2011‒2016, the observed incidence of anemia or pyrexia significantly decreased (trend test, p = 0.0009 for both). Generally, patient characteristics, drug use, and AE incidence between the DB and PMS were comparable; however, AEs such as neutropenia may require defining based on the laboratory data to achieve more comparable results in DBs. Besides the usefulness of healthcare claims DBs for long-term assessments, they may also serve as a good complementary to PMS in the pharmacovigilance of eribulin.

Sections du résumé

BACKGROUND BACKGROUND
To understand the extent to which a large-scale healthcare claims database (DB) captures the safety profile of eribulin mesylate (Halaven
METHODS METHODS
We descriptively summarized patient characteristics and AEs of 551 and 951 patients retrieved from DB and PMS, respectively, during 2011‒2013. Using 2814 patient data from the DB during 2011‒2016, the drug use and AE incidence over time were assessed.
RESULTS RESULTS
In both datasets, 99.8% were females, and the mean age was 57.8 ± 10.7 years. The mean number of eribulin administration was 11.1 ± 10.9 and 10.1 ± 7.8 in DB and PMS, respectively. Although, overall, the difference in AE incidence between the two datasets was moderate, gaps were larger for nausea (DB: 73.32% vs. PMS: 15.77%), neutropenia (20.87% vs. 66.67%), stomatitis (37.39% vs. 10.94%), and alopecia (0.36% vs. 12.09%). During 2011‒2016, the observed incidence of anemia or pyrexia significantly decreased (trend test, p = 0.0009 for both).
CONCLUSION CONCLUSIONS
Generally, patient characteristics, drug use, and AE incidence between the DB and PMS were comparable; however, AEs such as neutropenia may require defining based on the laboratory data to achieve more comparable results in DBs. Besides the usefulness of healthcare claims DBs for long-term assessments, they may also serve as a good complementary to PMS in the pharmacovigilance of eribulin.

Identifiants

pubmed: 30847841
doi: 10.1007/s40801-019-0150-8
pii: 10.1007/s40801-019-0150-8
pmc: PMC6423272
doi:

Types de publication

Journal Article

Langues

eng

Pagination

27-35

Références

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pubmed: 24420724
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pubmed: 28660549
Value Health Reg Issues. 2018 May;15:1-5
pubmed: 29474173
Breast Cancer. 2019 Mar;26(2):235-243
pubmed: 30324551

Auteurs

Yukinori Sakata (Y)

Clinical Planning and Development Department, Eisai Co., Ltd., 4-6-10, Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan. y2-sakata@hhc.eisai.co.jp.

Toshiyuki Matsuoka (T)

Clinical Planning and Development Department, Eisai Co., Ltd., 4-6-10, Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan.

Satoshi Ohashi (S)

Clinical Planning and Development Department, Eisai Co., Ltd., 4-6-10, Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan.

Tadashi Koga (T)

Clinical Study Support, Inc., Daiei Bldg, 2F, 1-11-20 Nishiki, Naka-ku, Nagoya, 460-0003, Japan.

Tetsumi Toyoda (T)

Clinical Study Support, Inc., Daiei Bldg, 2F, 1-11-20 Nishiki, Naka-ku, Nagoya, 460-0003, Japan.

Mika Ishii (M)

Clinical Planning and Development Department, Eisai Co., Ltd., 4-6-10, Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan.

Classifications MeSH