Evidence map›Paper›PMID 42287416›Full record

ArticleAnnals of hematology2026

Interleukin-6 levels decrease following rituximab treatment but increase following tocilizumab treatment.

Makoto Ide, Tetsuya Fukumoto, Hiroaki Ohnishi, Satoshi Okamura, Keitaro Kawano, Tomoko Yokoyama, Tomohiro Kameda

Abstract read
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Makoto IdeDepartment of Hematology, Takamatsu Red Cross Hospital, 4-1-3 Ban-cho, Takamatsu, 760-0017, Kagawa, Japan. makoto13@smile.ocn.ne.jp.ORCID http://orcid.org/0000-0002-5296-7518
Tetsuya FukumotoDepartment of Hematology, Takamatsu Red Cross Hospital, 4-1-3 Ban-cho, Takamatsu, 760-0017, Kagawa, Japan.
Hiroaki OhnishiDepartment of Hematology, Takamatsu Red Cross Hospital, 4-1-3 Ban-cho, Takamatsu, 760-0017, Kagawa, Japan.
Satoshi OkamuraDepartment of Hematology, Takamatsu Red Cross Hospital, 4-1-3 Ban-cho, Takamatsu, 760-0017, Kagawa, Japan.
Keitaro KawanoDepartment of Hematology, Takamatsu Red Cross Hospital, 4-1-3 Ban-cho, Takamatsu, 760-0017, Kagawa, Japan.
Tomoko YokoyamaDepartment of Nephrology, Takamatsu Red Cross Hospital, Takamatsu, Kagawa, Japan.
Tomohiro KamedaDepartment of Rheumatology, Takamatsu Red Cross Hospital, Takamatsu, Kagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic multicentric Castleman disease (iMCD) is a rare, gradually progressive lymphoproliferative disorder thought to arise from chronic hypercytokinemia, with IL-6 playing a central role in disease manifestations. C-reactive protein (CRP) levels are widely used as a surrogate marker of IL-6 activity in clinical practice. Although anti-IL-6 therapies, such as tocilizumab, are established treatments for iMCD, spurious elevation of circulating IL-6 levels after IL-6 pathway blockade has been reported, complicating biomarker interpretation. In contrast, changes in IL-6 and CRP levels following rituximab therapy remain poorly characterized, and direct comparisons between these therapeutic approaches are limited. Therefore, this retrospective study measured serum IL-6 and CRP levels in 17 patients (12 men and five women; mean age, 45 years) with iMCD before and after treatment with rituximab (n = 8) and tocilizumab (n = 9). Paired t test were used to assess in-group differences. After rituximab therapy, CRP values decreased from 67.7 ± 55.5 (range: 1.0-174.9) to 25.8 ± 29.0 (range: 1.0-71.2) mg/L, while IL-6 values decreased from 25.6 ± 29.7 (range: 1.3-86.8) to 12.0 ± 11.2 (range: 0.8-31.0) pg/mL (normal range < 8.0), although these reductions were not statistically significant. In contrast, tocilizumab therapy resulted in a significant decrease in CRP values decreased from 68.9 ± 40.8 (range: 24.0-147.9) to 7.9 ± 9.8 (range: 0.1-30.5) mg/L (p < 0.05), while IL-6 levels increased from 24.2 ± 7.3 (range: 14.0-37.0) to 749.2 ± 497.7 (range: 26.5-1720.0) pg/mL (normal range < 8.0) (p < 0.05). These findings indicate distinct biomarker dynamics, in which tocilizumab therapy led to elevated IL-6 levels, while rituximab improved iMCD symptoms by reducing IL-6 levels.

Indexed as

Antibodies, Monoclonal, HumanizedCastleman DiseaseInterleukin-6RituximabAdultAgedBiomarkersC-Reactive ProteinFemaleHumansMaleMiddle AgedRetrospective StudiesAntibodies, Monoclonal, HumanizedBiomarkersC-Reactive ProteinIL6 protein, humanInterleukin-6RituximabtocilizumabCastleman diseaseIL-6RituximabTAFRO syndromeTocilizumab

Identifiers

PMID42287416
PMCPMC13486046

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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.