Evidence map›Paper›PMID 30427585›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2019

Evaluation of the Short-, Mid-, and Long-Term Effects of Tofacitinib on Lymphocytes in Patients With Rheumatoid Arthritis.

Ronald van Vollenhoven, Eun Bong Lee, Sander Strengholt, Christopher Mojcik, Hernan Valdez, Sriram Krishnaswami, Pinaki Biswas, Irina Lazariciu, Anasuya Hazra, James D Clark and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
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  5. JAK/STAT inhibition reprograms T cell activation and metabolism in inflammatory arthritis patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  6. Article
  7. Article
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  9. Article
  10. Review
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  12. Potential Role of Upadacitinib in Cytomegalovirus Colitis Recurrence.European journal of case reports in internal medicine · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
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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

13 authors at 5 institutions in 4 countries.

Ronald van VollenhovenAmsterdam Rheumatology and Immunology Center, Amsterdam, The Netherlands.
Eun Bong LeeSeoul National University, Seoul, Republic of Korea.
Sander StrengholtPfizer Inc, New York, New York.
Christopher MojcikPfizer Inc, New York, New York.
Hernan ValdezPfizer Inc, New York, New York.
Sriram KrishnaswamiPfizer Inc, Groton, Connecticut.
Pinaki BiswasPfizer Inc, New York, New York.
Irina LazariciuIQVIA Canada, Montreal, Quebec, Canada.
Anasuya HazraPfizer Inc, Groton, Connecticut.
James D ClarkPfizer Inc, Cambridge, Massachusetts.
Jennifer HodgePfizer Inc, New York, New York.
Lisy WangPfizer Inc, Groton, Connecticut.
Ernest ChoyCardiff University School of Medicine, Cardiff, UK.
Pfizer (United States) · USCardiff University · GBIQVIA (United Kingdom) · GBSeoul National University · KRUniversity of Amsterdam · NL

Funding

Pfizer Inc
6 · The paper itself

Abstract

objectiveTofacitinib is an oral JAK inhibitor for the treatment of rheumatoid arthritis (RA). Altered lymphocyte cell counts and a potential association with increased infection rates have been reported in RA patients treated with JAK inhibitors. This analysis was undertaken to evaluate the short-, mid-, and long-term effects of tofacitinib on lymphocytes and infection rates in patients with RA.

methodsIn this post hoc analysis, absolute lymphocyte counts (ALCs) were obtained from phase III studies (12-24 months; n = 717-958) and phase I/II/III/long-term extension studies of tofacitinib (≤117 months) (All RA population; n = 7,061); lymphocyte subset counts (LSCs) were from phase II studies (1.5-6 months' exposure; n = 236-486), an ORAL Sequel vaccine substudy (~22 months; n = 198), and an ORAL Sequel lymphocyte substudy (~50 months; n = 55-1,035) of tofacitinib. The reversibility of ALC/LSC changes was evaluated. The relationship of ALC and LSC to infections was analyzed in the All RA population. The value of monitoring ALC alone was assessed by examining correlations between ALCs and LSCs.

resultsTofacitinib treatment resulted in an initial increase in ALC versus pretreatment baseline, which gradually declined to steady state by ~48 months. CD4+ and CD8+ T cell counts decreased over long-term treatment, and ALC and LSC changes were reversible upon treatment cessation. Patients with ALCs of <500 cells/mm

conclusionOur findings indicate that monitoring of ALC alone appears to be adequate to assess infection risk in tofacitinib-treated patients with RA.

Indexed as

B-LymphocytesKiller Cells, NaturalLymphocyte CountT-LymphocytesArthritis, RheumatoidCD4 Lymphocyte CountCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesHumansIncidenceInfectionsJanus Kinase InhibitorsPiperidinesPyrimidinesPyrrolesTime FactorsJanus Kinase InhibitorsPiperidinesPyrimidinesPyrrolestofacitinib

Identifiers

PMID30427585
PMCPMC6593802
OpenAlexW2901433867

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.