Management of hepatitis B reactivation in lymphoma patients on rituximab with past hepatitis B exposure: An observational study.


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Jul 2019
Historique:
pubmed: 21 3 2018
medline: 10 7 2019
entrez: 21 3 2018
Statut: ppublish

Résumé

Currently, a standardized approach to prevent and manage hepatitis B reactivation in lymphoma patients with past hepatitis exposure receiving rituximab in Singapore is lacking. This study is designed to report the current management approach and outcomes associated with hepatitis B reactivation. The primary objective was to report 6-, 12-, 24-month cumulative hepatitis B reactivation-related outcomes. Secondary objectives were to report monitoring frequencies of hepatitis B DNA and liver function tests performed in lymphoma patients with resolved hepatitis B receiving rituximab, and anti-viral prophylaxis use. This was a single centre, retrospective observational study. Patients with resolved hepatitis B initiated on rituximab from January 2011 to December 2015 were identified and reviewed over a two-year period starting from the date of rituximab initiation. Relevant parameters were obtained from electronic medical records. Hepatitis B reactivation was defined by hepatitis B DNA levels 20 IU/ml (1.30 log/ml) and above. Data were analysed using descriptive statistics. Seventy-five patients were retrospectively reviewed over a two-year period. Hepatitis B reactivation was defined as hepatitis B DNA levels ≥20 IU/ml (1.30 log/ml). The 24-month cumulative hepatitis B reactivation rate was 4.0%. The median (interquartile range) number of hepatitis B DNA tests performed during treatment, initial six-month follow-up, and subsequent follow-up were 1.0 (0.0-2.6), 1.0 (0.0-2.0), and 1.0 (0.0-3.1), respectively. Large variations in hepatitis B reactivation monitoring and management strategies were observed. Further studies are required to develop and determine a standardised protocol that could contribute to safer and more cost-effective care for lymphoma patients with resolved hepatitis B on rituximab.

Sections du résumé

BACKGROUND BACKGROUND
Currently, a standardized approach to prevent and manage hepatitis B reactivation in lymphoma patients with past hepatitis exposure receiving rituximab in Singapore is lacking. This study is designed to report the current management approach and outcomes associated with hepatitis B reactivation.
OBJECTIVES OBJECTIVE
The primary objective was to report 6-, 12-, 24-month cumulative hepatitis B reactivation-related outcomes. Secondary objectives were to report monitoring frequencies of hepatitis B DNA and liver function tests performed in lymphoma patients with resolved hepatitis B receiving rituximab, and anti-viral prophylaxis use.
METHODOLOGY METHODS
This was a single centre, retrospective observational study. Patients with resolved hepatitis B initiated on rituximab from January 2011 to December 2015 were identified and reviewed over a two-year period starting from the date of rituximab initiation. Relevant parameters were obtained from electronic medical records. Hepatitis B reactivation was defined by hepatitis B DNA levels 20 IU/ml (1.30 log/ml) and above. Data were analysed using descriptive statistics.
RESULTS RESULTS
Seventy-five patients were retrospectively reviewed over a two-year period. Hepatitis B reactivation was defined as hepatitis B DNA levels ≥20 IU/ml (1.30 log/ml). The 24-month cumulative hepatitis B reactivation rate was 4.0%. The median (interquartile range) number of hepatitis B DNA tests performed during treatment, initial six-month follow-up, and subsequent follow-up were 1.0 (0.0-2.6), 1.0 (0.0-2.0), and 1.0 (0.0-3.1), respectively.
CONCLUSION CONCLUSIONS
Large variations in hepatitis B reactivation monitoring and management strategies were observed. Further studies are required to develop and determine a standardised protocol that could contribute to safer and more cost-effective care for lymphoma patients with resolved hepatitis B on rituximab.

Identifiants

pubmed: 29554828
doi: 10.1177/1078155218763039
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Rituximab 4F4X42SYQ6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1042-1052

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Denise Yeo (D)

1 Department of Pharmacy, National University of Singapore, Singapore.

Ihtimam Hossain (I)

2 Department of Pharmacy, Singapore General Hospital, Singapore.

Soon Thye Lim (ST)

3 Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Mohamad Farid (M)

3 Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Miriam Tao (M)

3 Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Richard Quek (R)

3 Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Tiffany Tang (T)

3 Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Alexandre Chan (A)

1 Department of Pharmacy, National University of Singapore, Singapore.
4 Department of Pharmacy, National Cancer Centre Singapore, Singapore.

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Classifications MeSH