Evidence map›Paper›PMID 36385738›Full record

ArticleClinical and translational science2023

Safety and tolerability of a 90-minute rapid infusion of Sandoz biosimilar rituximab in B-cell lymphoproliferative disorders in a real-world setting.

Ana Muntañola, José María Arguiñano-Pérez, Julio Dávila, Sonia González de Villambrosia, Cecilia Carpio, Ana Jiménez-Ubieto, Antonio Salar, GELTAMO (Grupo español de linfomas y trasplante de médula ósea)

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 7 institutions in 2 countries.

Ana MuntañolaDepartment of Hematology, Hospital Universitari Mutua Terrassa, Terrassa, Spain.
José María Arguiñano-PérezDepartment of Hematology, Hospital Universitario de Navarra, Pamplona, Spain.
Julio DávilaDepartment of Hematology, Complejo Asistencial de Ávila, Ávila, Spain.
Sonia González de VillambrosiaDepartment of Hematology, Hospital Universitario Marqués de Valdecilla/IDIVAL, Santander, Spain.
Cecilia CarpioDepartment of Hematology, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Barcelona, Spain.
Ana Jiménez-UbietoDepartment of Hematology, Hospital 12 de Octubre, Madrid, Spain.
Antonio SalarDepartment of Hematology, Hospital del Mar, Barcelona, Spain.ORCID 0000-0002-4652-4825
GELTAMO (Grupo español de linfomas y trasplante de médula ósea)
Catholic University of Ávila · ESComplejo Hospitalario de Navarra · ESHebron University · PSInstituto de Investigación Marqués de Valdecilla · ESMútua Terrassa · ESResearch Institute Hospital 12 de Octubre · ESUniversitat Pompeu Fabra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although rituximab is generally well-tolerated, infusion-related reactions (IRRs) are common with the initial dose when administered intravenously according to standard recommendations. To prevent IRRs, premedication and low-speed infusion rates have been recommended. Consequently, intravenous (i.v.) infusion of rituximab can become a labor-intensive process. Rapid i.v. rituximab infusion over 90 min has demonstrated a favorable safety profile for the second and subsequent infusions during the course of therapy. The aim of this study was to investigate the safety and tolerability of 90-min rapid infusion of Sandoz rituximab biosimilar (SDZ-RTX) for patients with CD20+ lymphoma or chronic lymphocytic leukemia (CLL). We retrospectively reviewed all patients with CD20+ lymphoma or CLL who received SDZ-RTX infusions in 90 min from July 2019 to July 2021 at seven Spanish hospitals. The primary end point was the incidence of IRRs. We identified 124 patients and 576 rapid administrations of SDZ-RTX, with an average of five rapid infusions per patient. Most rapid infusions of SDZ-RTX were in combination with CHOP/CHOP-like therapy (48.4%), followed by SDZ-RTX alone (15.1%), in combination with bendamustine (14.5%), or with other regimens (22%). The 90-min SDZ-RTX infusion schedule was well-tolerated with no grade 3/4 IRRs. The incidence of any grade IRR during the first rapid infusion was 1% (5 grade 1 IRRs and 1 grade 2 IRR). In conclusion, rapid 90-min i.v. administration of SDZ-RTX for the second and subsequent infusions during the course of therapy is well-tolerated in patients with CD20+ lymphoma or CLL.

Indexed as

Biosimilar PharmaceuticalsLeukemia, Lymphocytic, Chronic, B-CellAntibodies, Monoclonal, Murine-DerivedHumansRetrospective StudiesRituximabAntibodies, Monoclonal, Murine-DerivedBiosimilar PharmaceuticalsRituximab

Identifiers

PMID36385738
PMCPMC9926065
OpenAlexW4309246188

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.