Evidence map›Paper›PMID 27075017›Full record

ReviewInvestigational new drugs2016

CD20-targeting in B-cell malignancies: novel prospects for antibodies and combination therapies.

Yaghoub Safdari, Vahideh Ahmadzadeh, Safar Farajnia

Abstract readReview
PubMed Publisher
In one paragraph

Review in Investigational new drugs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. CD20-positive extranodal NK/T cell lymphoma: clinicopathologic and prognostic features.Virchows Archiv : an international journal of pathology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. 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

3 authors at 3 institutions in 1 country.

Yaghoub SafdariCellular and Molecular Research Center, Taleghani Children Hospital, Gorgan University of Medical Sciences, Gorgan, Iran.
Vahideh AhmadzadehBiotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. vahideh_ahmadzadeh@yahoo.com.
Safar FarajniaBiotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Biotechnology Research Center · IRGolestan University · IRTabriz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression of CD20 antigen by the most of transformed B cells is believed to be the driving force for targeting this molecule by using anti-CD20 monoclonal antibodies. While it is true that most lymphoma/leukemia patients can be cured, these regimens are limited by the emergence of treatment resistance. Based on these observations, development of anti-CD20 monoclonal antibodies and combination therapies have been recently proposed, in particular with the aim to optimize the cytotoxic activity. Here we outline a range of new experimental agents concerning the CD20 positive B-cell tumors which provide high benefit from conventional therapy.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD20Antineoplastic Combined Chemotherapy ProtocolsB-LymphocytesHumansLymphoma, Non-HodgkinAntibodies, MonoclonalAntigens, CD20Antibody-based therapeuticsB-cell malignanciesCD20 antigenCombination therapy

Identifiers

PMID27075017
OpenAlexW2336749327

What OpenQuestion holds

Textmetadata
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.