Real word evidence on rituximab utilization: Combining administrative and hospital-pharmacy data.
Administration, Intravenous
Administrative Claims, Healthcare
/ statistics & numerical data
Adolescent
Adult
Aged
Antineoplastic Agents, Immunological
/ administration & dosage
Databases, Factual
/ statistics & numerical data
Drug Utilization
/ statistics & numerical data
Female
Follow-Up Studies
Humans
Infections
/ chemically induced
Italy
/ epidemiology
Kaplan-Meier Estimate
Leukemia, Lymphocytic, Chronic, B-Cell
/ drug therapy
Longitudinal Studies
Lymphoma, Non-Hodgkin
/ drug therapy
Male
Middle Aged
Pharmacy Service, Hospital
/ statistics & numerical data
Retrospective Studies
Rituximab
/ administration & dosage
Time Factors
Treatment Outcome
Young Adult
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
28
10
2019
accepted:
17
02
2020
entrez:
13
3
2020
pubmed:
13
3
2020
medline:
18
6
2020
Statut:
epublish
Résumé
To describe patterns of utilization, survival and infectious events in patients treated with rituximab at the University Hospital of Siena (UHS) to explore the feasibility of combining routinely collected administrative and hospital-pharmacy data for examining the real-world use of intravenous antineoplastic drugs. A retrospective, longitudinal cohort study was conducted using data from the Hospital Pharmacy of Siena (HPS) and the Regional Administrative Database of Tuscany (RAD). Patients aged ≥18 years with ≥1 rituximab administration recorded between January 2012 and June 2016 were identified in the HPS database. Anonymized patient-level data were linked to RAD. Rituximab utilization during the first year of treatment was described using HPS. Hospital diagnoses of adverse infectious events that occurred during the first year of follow-up and four-year survival were observed using RAD. A total of 311 new users of rituximab were identified: 264 patients received rituximab for non-Hodgkin's lymphoma (NHL) and 47 were treated for chronic lymphocytic leukemia (CLL). Among new users with one complete year of follow-up (n = 203) over 95% received rituximab as the first-line treatment, and approximately 70% of them received 5-8 doses. No patient in the CLL group received >8 administrations. Four-year survival was approximately 70% in both CLL and NHL patients. Sepsis was the most frequent infectious event observed (5.1%). HPS and RAD provided complementary information on rituximab utilization, demonstrating their potential for future pharmacoepidemiological studies on antineoplastic medications administered in the Italian hospital setting. Overall, this general description of the real-world utilization of rituximab in patients treated for NHL and CLL at UHS was in line with treatment guidelines and current knowledge on the rituximab safety profile.
Identifiants
pubmed: 32163477
doi: 10.1371/journal.pone.0229973
pii: PONE-D-19-30012
pmc: PMC7067445
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Rituximab
4F4X42SYQ6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0229973Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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