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Severe infusion-related reactions are uncommon in rituximab-treated CLL patients in clinical practice: Results from a Swedish national observational study

Norin, Stefan (author)
Karolinska Institutet
Bjorkstrand, Bo (author)
Karolinska University Hospital, Sweden; Karolinska Institute, Sweden
Rommel, Franz (author)
Region Östergötland, Hematologiska kliniken US
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Timberg, Lars (author)
Kristianstad Central Hospital, Sweden
Andersson, Per-Ola (author)
Sahlgrens University Hospital, Sweden
Haggstrom, Johan (author)
Kalmar Hospital, Sweden
Aldrin, Anders (author)
Visby Hospital, Sweden
Hansson, Lotta (author)
Karolinska Institutet
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 (creator_code:org_t)
Elsevier, 2015
2015
English.
In: Leukemia Research. - : Elsevier. - 0145-2126 .- 1873-5835. ; 39:1, s. 33-37
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • There have been concerns about serious infusion-related adverse drug reactions (ADR) with rituximabin chronic lymphocytic leukemia (CLL). We therefore conducted an observational trial in which CLL patients planned for rituximab-containing therapy were eligible. Ninety-six patients from 19 centers were enrolled. The most common regimen was rituximab, fludarabine and cyclophosphamide. Fifty-six patients experienced ADR during rituximab infusion. Reactions greater than= grade 3 occurred in five patients and no cases of tumor lysis syndrome were recorded. Despite a high number of circulating tumor cells few severe ADR were noted. Thus, rituximab containing regimens can be considered safe for CLL patients in general practice.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Keyword

Adverse reaction; Chronic lymphocytic leukemia; Rituximab; Therapy

Publication and Content Type

ref (subject category)
art (subject category)

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