Evidence map›Paper›PMID 42226886›Full record

ArticleJournal of blood medicine2026

Malignancy-Associated Hemophagocytic Lymphohistiocytosis: An Experience of 15 Years in Polish Pediatric Hematology Centers.

Magdalena Wolowiec, Katarzyna Drabko, Lucyna Maciejka-Kemblowska, Ninela Irga-Jaworska, Katarzyna Smalisz, Szymon Skoczen, Renata Tomaszewska, Tomasz Szczepanski, Katarzyna Babol-Pokora, Wojciech Mlynarski and 4 more

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

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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

14 authors.

Magdalena WolowiecDepartment of Oncology, Pediatric Hematology, Clinical Transplantology, Pediatrics and Rare Diseases, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-0770-1630
Katarzyna DrabkoDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, Lublin, Poland.ORCID 0000-0002-7094-9129
Lucyna Maciejka-KemblowskaDepartment of Pediatrics, Pediatric Hematology and Oncology, Medical University of Gdansk, Gdansk, Poland.ORCID 0000-0002-8458-4722
Ninela Irga-JaworskaDepartment of Pediatrics, Pediatric Hematology and Oncology, Medical University of Gdansk, Gdansk, Poland.ORCID 0000-0002-7637-4397
Katarzyna SmaliszDepartment of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.ORCID 0009-0009-2201-8766
Szymon SkoczenDepartment of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.ORCID 0000-0001-6867-2717
Renata TomaszewskaDepartment of Pediatrics, Pediatric Hematology and Oncology, Silesian Medical University, Zabrze, Poland.ORCID 0000-0003-2801-9216
Tomasz SzczepanskiDepartment of Pediatrics, Pediatric Hematology and Oncology, Silesian Medical University, Zabrze, Poland.ORCID 0000-0001-5336-261X
Katarzyna Babol-PokoraDepartment of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.ORCID 0000-0002-9836-9118
Wojciech MlynarskiDepartment of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.ORCID 0000-0003-2714-5851
Katarzyna PopkoDepartment of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-1281-4357
Urszula DemkowDepartment of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0003-0674-9824
Konrad FurmanczykDepartment of Applied Mathematics, Warsaw University of Life Sciences, Warsaw, Poland.ORCID 0000-0002-7683-4787
Iwona MalinowskaDepartment of Oncology, Pediatric Hematology, Clinical Transplantology, Pediatrics and Rare Diseases, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0003-0671-7849

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: M-HLH is a type of HLH that most often occurs in children in the course of hematological malignancies. The diagnosis is based on meeting the criteria of the HLH-2004 Protocol. The disease has a rapid course, and the lack of proper diagnosis and treatment threatens the patient's life. Methods: The paper presents the thorough clinical characteristics, course of treatment, and treatment results in 23 patients treated in pediatric hemato-oncology centers in Poland and reported to Polish HLH registry. HLH diagnostic criteria, CNS involvement, coexisting viral infections, genetic test results, treatment modalities, therapeutic responses, relapse incidence, and final outcomes were analyzed. Clinical and laboratory factors were subjected to statistical analysis. Overall survival was estimated using the Kaplan-Meier method for the entire cohort and separately for subgroups defined by type of malignancy and treatment strategy. Separate univariable Cox proportional hazards models were used to explore the association between selected clinical factors and survival. Results: The median age at diagnosis was 11.7 years, in 8 patients HLH symptoms preceded the cancer diagnosis. Acute leukemia was the factor causing M-HLH in 12 patients, in the remaining patients it was lymphoma. The treatment included tumor-directed therapy with or without HLH-directed therapy. The probability of survival in the study group was 0.539 (95% CI 0.364-0.798). Remission of HLH was statistically significant (p-value = 0.0007) and reduced the risk of death by 90% (HR=0.10). Conclusion: Quick and precise diagnosis and implementation of appropriate treatment bringing the patient into HLH remission is extremely important for survival.

Indexed as

hemophagocytic lymphohistiocytosisHLHHLH-directed therapyleukemialymphomamalignancy

Identifiers

PMID42226886
PMCPMC13222552

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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.