Evidence map›Paper›PMID 28983798›Full record

ReviewAdvances in therapy2017

Rituximab in B-Cell Hematologic Malignancies: A Review of 20 Years of Clinical Experience.

Gilles Salles, Martin Barrett, Robin Foà, Joerg Maurer, Susan O'Brien, Nancy Valente, Michael Wenger, David G Maloney

Open access · hybridAbstract readHistorical ArticleReview
In one paragraph

Review in Advances in therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 352 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
352citing papers in PubMed, 5 pooled it
20.2field-weighted citation impact, top 1% 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

352 citing papers in PubMed, 5 syntheses or guidelines pooled it, 590 citations in OpenAlex.

  1. Pooled it
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  5. [Efficacy and safety of rituximab in children and adolescents with mature B-cell non-Hodgkin's lymphoma: a Meta analysis].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Pooled it
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  13. Engineering the subcutaneous delivery of antibody-drug conjugates.Journal of controlled release : official journal of the Controlled Release Society · 2026
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292 more citing papers are in PubMed but not listed here.

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 6 institutions in 5 countries.

Gilles SallesHématologie, Hospices Civils de Lyon and Université de Lyon, Pierre-Bénite, Lyon, France. gilles.salles@chu-lyon.fr.ORCID 0000-0002-9541-8666
Martin BarrettRoche Products Ltd., Welwyn Garden City, UK.
Robin FoàDepartment of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.
Joerg MaurerF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Susan O'BrienChao Family Comprehensive Cancer Center, University of California, Irvine, Orange, CA, USA.
Nancy ValenteGenentech Inc., South San Francisco, CA, USA.
Michael WengerF. Hoffmann-La Roche Ltd., Basel, Switzerland.
David G MaloneyFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Roche (Switzerland) · CHFred Hutch Cancer Center · USRoche (United Kingdom) · GBSapienza University of Rome · ITUniversité Claude Bernard Lyon 1 · FRUniversity of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rituximab is a human/murine, chimeric anti-CD20 monoclonal antibody with established efficacy, and a favorable and well-defined safety profile in patients with various CD20-expressing lymphoid malignancies, including indolent and aggressive forms of B-cell non-Hodgkin lymphoma. Since its first approval 20 years ago, intravenously administered rituximab has revolutionized the treatment of B-cell malignancies and has become a standard component of care for follicular lymphoma, diffuse large B-cell lymphoma, chronic lymphocytic leukemia, and mantle cell lymphoma. For all of these diseases, clinical trials have demonstrated that rituximab not only prolongs the time to disease progression but also extends overall survival. Efficacy benefits have also been shown in patients with marginal zone lymphoma and in more aggressive diseases such as Burkitt lymphoma. Although the proven clinical efficacy and success of rituximab has led to the development of other anti-CD20 monoclonal antibodies in recent years (e.g., obinutuzumab, ofatumumab, veltuzumab, and ocrelizumab), rituximab is likely to maintain a position within the therapeutic armamentarium because it is well established with a long history of successful clinical use. Furthermore, a subcutaneous formulation of the drug has been approved both in the EU and in the USA for the treatment of B-cell malignancies. Using the wealth of data published on rituximab during the last two decades, we review the preclinical development of rituximab and the clinical experience gained in the treatment of hematologic B-cell malignancies, with a focus on the well-established intravenous route of administration. This article is a companion paper to A. Davies, et al., which is also published in this issue.

fundingF. Hoffmann-La Roche Ltd., Basel, Switzerland.

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalB-LymphocytesHematologic NeoplasmsHistory, 20th CenturyHistory, 21st CenturyHumansLymphoma, B-CellRituximabAntineoplastic Agents, ImmunologicalRituximabB-cell lymphomaCD20Chronic lymphocytic leukemiaDiffuse large B-cell lymphomaFollicular lymphomaMonoclonal antibodyNon-Hodgkin lymphomaRituximabSafetyTreatment outcome

Identifiers

PMID28983798
PMCPMC5656728
OpenAlexW2760907988

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.