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Subcutaneous immunoglobulin in lymphoproliferative disorders and rituximab-related secondary hypogammaglobulinemia: a single-center experience in 61 patients.

Articolo
Data di Pubblicazione:
2014
Abstract:
Intravenous immunoglobulin replacement therapy represents the standard treatment for hypogammaglobulinemia secondary to B-cell lymphoproliferative disorders. Subcutaneous immunoglobulin infusion is an effective, safe and well-tolerated treatment approach in primary immunodeficiencies but no extensive data are available on their use in secondary hypogammaglobulinemia, a frequent phenomenon occurring after treatment with anti-CD20 monoclonal antibodies in lymphoproliferative disorders. In this retrospective study we evaluated efficacy (serum IgG trough levels, incidence of infections/year, need for antibiotics) and safety (number of adverse events) of intravenous (300 mg/kg/4 weeks) vs subcutaneous (75 mg/kg/week) immunoglobulin replacement therapy in 61 patients. In addition, the impact of the infusion methods on the quality of life was compared. All patients were treated with subcutaneous immunoglobulin, and 33 out of them were previously treated with intravenous immunoglobulin. Both treatments appeared to be effective in replacing Ig production deficiency and in reducing the incidence of infectious events and the need for antibiotics; subcutaneous immunoglobulin obtained a superior benefit when compared to intravenous immunoglobulin achieving higher IgG trough levels, lower incidence of overall infection and need for antibiotics; the incidence of serious bacterial infections was similar with both infusion ways. As expected, a lower number of adverse events was registered with subcutaneous immunoglobulin, compared to intravenous immunoglobulin, with no serious adverse events. Finally, we observed an improvement in health-related quality of life parameters after the switch to subcutaneous immunoglobulin. Our results suggest that subcutaneous immunoglobulin are safe and effective in patients with hypogammaglobulinemia associated to lymphoproliferative disorders.
Tipologia CRIS:
01.01 - Articolo in rivista
Elenco autori:
Compagno, Nicolo'; Cinetto, Francesco; Semenzato, GIANPIETRO CARLO; Agostini, Carlo
Autori di Ateneo:
AGOSTINI CARLO
CINETTO FRANCESCO
SEMENZATO GIANPIETRO CARLO
Link alla scheda completa:
https://www.research.unipd.it/handle/11577/2827600
Link al Full Text:
https://www.research.unipd.it//retrieve/handle/11577/2827600/20695/haematol.2013.101261.full.pdf
https://www.research.unipd.it//retrieve/handle/11577/2827600/582930/7052-Article%20Text-42732-1-10-20200723.pdf
Pubblicato in:
HAEMATOLOGICA
Journal
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