Evidence map›Paper›PMID 42397658›Full record

ArticleImmunologic research2026

Emapalumab plus conventional therapy with or without ruxolitinib for pediatric hemophagocytic lymphohistiocytosis: a single center retrospective study.

Meiling Liao, Li Xiao, Min Gu, Jie Yu

Abstract read
PubMed Publisher
In one paragraph

Article in Immunologic research, 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

4 authors.

Meiling LiaoDepartment of Hematology & Oncology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatric Metabolism and Inflammatory Diseases, Chongqing, China.
Li XiaoBig Data Center for Children's Medical Care Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Intelligent Application of Big Data in Pediatrics Engineering Research Center of Chongqing Education Commission of China, Chongqing, China.
Min GuDepartment of Hematology & Oncology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatric Metabolism and Inflammatory Diseases, Chongqing, China.
Jie YuDepartment of Hematology & Oncology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatric Metabolism and Inflammatory Diseases, Chongqing, China. yjetyy@163.com.ORCID http://orcid.org/0000-0003-3590-2701

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemophagocytic lymphohistiocytosis (HLH) is a rare, highly fatal hyperinflammatory syndrome characterized by an uncontrolled cytokine cascade. Traditional chemotherapy leaves 30% of patients unresponsive, and its side effects are significant. Precise targeted therapies are highly anticipated. Emapalumab is a monoclonal antibody targeting interferon-γ, while ruxolitinib is a JAK1/2 inhibitor, and their application in HLH treatment is gaining attention.

methodsWe retrospectively collected clinical data from pediatric HLH patients who received emapalumab added to conventional therapy, with or without ruxolitinib, at our hospital between June 1, 2022, and June 1, 2024. Treatment efficacy, safety, improvement in clinical parameters, and causes of death were analyzed.

resultsA total of 10 pediatric patients were included: 7 with refractory disease, 2 with relapsed disease, and 1 with newly diagnosed disease. EBV-associated HLH was observed in 6 of the 10 patients. All patients received emapalumab added to conventional therapy, and 7 patients additionally received ruxolitinib. The median follow-up duration was 164 days (range, 19-473 days). Among the 10 patients, 5 achieved remission. The response rates for fever, hypofibrinogenemia, neutropenia, hyperbilirubinemia, and elevated transaminases were 6/6, 5/5, 8/9, 4/7, and 6/10, respectively. Among patients with relapsed/refractory disease, the remission rate was 2/3 with emapalumab plus conventional therapy alone and 2/6 with the further addition of ruxolitinib. In patients with non-EBV-associated HLH, the corresponding remission rates were 1/2 and 2/2, respectively. In patients with EBV-associated HLH, the rates were 1/1 and 1/5, respectively.

conclusionsIn this small-sample retrospective study, emapalumab showed a more pronounced trend toward alleviating fever, hypofibrinogenemia, and neutropenia than toward improving liver function among pediatric HLH patients. Adding ruxolitinib to the combination of emapalumab and conventional therapy did not demonstrate a clear additional clinical benefit, particularly in the EBV-associated HLH and relapsed/refractory subgroups. These findings are constrained by the study design and sample size and necessitate validation in larger, prospective studies.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedLymphohistiocytosis, HemophagocyticNitrilesPyrazolesPyrimidinesAdolescentAntibodies, NeutralizingChildChild, PreschoolDrug Therapy, CombinationFemaleHumansInfantMaleRetrospective StudiesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingEmapalumabNitrilesPyrazolesPyrimidinesruxolitinibConventional therapyEBVEmapalumabPediatric hemophagocytic lymphohistiocytosisRuxolitinib

Identifiers

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.