Evidence map›Paper›PMID 42560429›Full record

ArticleAnnals of hematology2026

Long-term follow-up of ruxolitinib pre-approval use in acute and chronic graft-versus-host disease.

Raphael Loisl, Anna Bauhofer, Alexander Nikoloudis, Robert Milanov, Sigrid Machherndl-Spandl, Veronika Buxhofer-Ausch, Michaela Binder, Petra Hasengruber, Emine Kaynak, Dagmar Wipplinger and 7 more

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

17 authors.

Raphael LoislDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria. raphael.loisl@ukr.de.
Anna BauhoferDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria. anna.bauhofer@ordensklinikum.at.ORCID http://orcid.org/0000-0003-2943-4614
Alexander NikoloudisDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Robert MilanovDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Sigrid Machherndl-SpandlDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Veronika Buxhofer-AuschDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Michaela BinderDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Petra HasengruberDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Emine KaynakDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Dagmar WipplingerDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Irene StrasslDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Olga SainiMedical Faculty, Johannes Kepler University, Linz, Austria.
Christoph AichingerDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Andreas PetzerDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.
Hildegard GreinixDepartment of Internal Medicine, Division of Hematology, Medical University of Graz, Graz, Austria.
Daniel WolffDepartment of Internal Medicine III, Hematology and Medical Oncology, University Hospital Regensburg, Franz-Josef-Strauß-Allee 11, Regensburg, 93053, Germany.
Johannes ClausenDepartment of Internal Medicine I: Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz - Elisabethinen, Fadingerstraße 1, Linz, 4020, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Steroid-refractory (SR) acute and chronic graft-versus-host disease (aGVHD/cGVHD) are frequent and serious complications after allogeneic hematopoietic stem cell transplantation. Ruxolitinib (RUX) is approved for the treatment of both conditions. Real world evidence may provide valuable complementary information beyond prospective trials because of significant divergences in study populations, endpoints, treatment strategies, and observation time. We report long-term outcomes of 118 patients with acute (n = 61), classic chronic (n = 43) and overlap chronic GVHD (n = 14) who received RUX within a named-patient-program in the pre-approval era as second-line treatment or beyond. In 22 patients, GVHD occurred after donor lymphocyte infusion (DLI). The cohort included heavily pretreated patients, with 26.2% of aGVHD in 3rd -line or beyond, and 29.8% of cGVHD in 4th -line or beyond. Only 22 patients (18.6%) met all in-/exclusion criteria of the respective pivotal phase III studies. The most frequent incompatibilities were unmet SR criteria, excessive pretreatment, previous DLI, overlap chronic GVHD, and medical/hematological criteria. Overall response rate to RUX was 68.9% in aGVHD, and 66.7% in cGVHD. In all three GVHD types, > 50% of patients were able to discontinue systemic steroids. With a survivors' median follow up of 60.3 months (range, 25.5-99.3) from RUX initiation, 4-year survival probability was 57.4% in aGVHD, 81.1% in classic cGVHD, and 78.6% in overlap cGVHD. Our findings reveal favorable survival probabilities associated with a long-term steroid-sparing/replacing potential of RUX in treatment-refractory aGVHD and cGVHD, including overlap syndrome and DLI-associated GVHD.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationPyrazolesAcute DiseaseAdolescentAdultAgedChronic DiseaseFemaleFollow-Up StudiesHumansMaleMiddle AgedNitrilesPyrimidinesTransplantation, HomologousNitrilesPyrazolesPyrimidinesruxolitinibDonor lymphocyte infusion (DLI)Hematopoietic stem cell transplantationOverlap GVHDRefractory graft versus host diseaseRuxolitinib

Identifiers

PMID42560429
PMCPMC13447468

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.