Evidence map›Paper›PMID 42523406›Full record

ArticlemedRxiv : the preprint server for health sciences2026

MAGIC Composite Score Predicts Outcomes of Second-Line Therapy for Acute GVHD.

Tara Sebastian, Daniela Weber, Aaron M Etra, Ingrid Vasova, Francis Ayuk, Hannah K Choe, Zachariah DeFilipp, Francesco Quagliarella, Karni Bedirian, Márcio Augusto Diniz and 25 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

35 authors.

Tara SebastianDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Daniela WeberDepartment of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany.
Aaron M EtraDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Ingrid VasovaDepartment of Internal Medicine 5, Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany.
Francis AyukDepartment of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Hannah K ChoeDivision of Hematology, Blood and Marrow Transplantation Program, The Ohio State University Comprehensive Cancer Center, Columbus, OH.
Zachariah DeFilippHematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
Francesco QuagliarellaDepartment of Pediatric Hematology/Oncology and of Cell and Gene Therapy, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
Karni BedirianDepartment of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY.
Márcio Augusto DinizDepartment of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY.
Paibel Aguayo-HiraldoDivision of Bone Marrow Transplantation, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA.
Peter BaderDivision of Stem Cell Transplantation and Immunology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt, Germany.
Janna BaezDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Chantiya ChanswangphuwanaDivision of Hematology and Center of Excellence in Translational Hematology, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Gilbert EngDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Thomas FranckeDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Elizabeth O HexnerDepartment of Medicine and Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Nikolaos KatsivelosDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Carrie L KitkoPediatric Hematology/Oncology Division, Vanderbilt University Medical Center, Nashville, TN.
Sabrina KrausDepartment of Internal Medicine II, University Hospital of Würzburg, Würzburg, Germany.
Ioannis E LouloudisDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
George MoralesDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Ryotaro NakamuraDepartment of Hematology/Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Timothy S OlsonDivision of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.
Muna QayedDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Pavan ReddyBaylor College of Medicine, Dan Duncan Cancer Center, Houston, TX.
Ran ReshefDivision of Hematology/Oncology and Columbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY.
Tal SchechterDivision of Hematology/Oncology/Blood and Marrow Transplant, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Tingyu WangDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Matthias WölflDepartment of Pediatrics, Children's Hospital, University Hospital of Würzburg, Würzburg, Germany.
Rachel YoungDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Robert ZeiserDepartment of Medicine I, University of Freiburg Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
William J HoganDivision of Hematology, Mayo Clinic, Rochester, MN.
John E LevineDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.
James L M FerraraDivision of Hematology/Medical Oncology, The Tisch Cancer Center, Icahn School of Medicine at Mount Sinai, New York, NY.

Funding

TUMOR VACCINES AND BONE MARROW TRANSPLANTATIONP01CA039542 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JOHN LEVINE · 1985 to 2026
$47.9M
THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ramon E Parsons · 2015 to 2026
$35.4M
Mount Sinai StARR Program - NIAIDR38AI181012 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BENJAMIN K CHEN, Jaime C Chu · 2024 to 2026
$918k
Validation of a novel and more accurate endpoint for GVHD clinical trialsR21HL177578 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI JOHN LEVINE · 2025 to 2026
$254k
NCI NIH HHS P01 CA039542NCI NIH HHS P30 CA196521NHLBI NIH HHS R21 HL177578NIAID NIH HHS R38 AI181012
6 · The paper itself

Abstract

Approximately 30% of patients with acute graft-versus-host disease (GVHD) develop steroid-refractory disease and have very poor outcomes. Ruxolitinib has become the standard of care for steroid-refractory acute GVHD, but it is unclear which patients derive benefit. The MAGIC Composite Score (MCS), an algorithm that combines clinical symptoms and biomarkers, has been validated to predict outcomes at the start of primary GVHD treatment. Here, we evaluated its performance at the initiation of second-line treatment in 278 patients. MCS stratified patients into three risk groups (MCS1-3), with the majority (88%) classified as intermediate or high risk. Increasing MCS score was associated with progressively higher 1-year non-relapse mortality (NRM) rates (16%, 41%, and 73%; p<0.001), lower 1-year survival (77%, 56%, and 24%; p<0.001), and lower complete response (CR) rates at day 28 (47%, 38%, and 20%, respectively; p<0.01). The area under the receiver operating characteristic curve (AUROC) for 1-year NRM was significantly higher with MCS compared to clinical symptoms alone (0.70 vs. 0.63; p=0.023). Among patients treated with ruxolitinib, higher MCS similarly predicted higher NRM and lower survival and CR rates. Patients classified as MCS2/3 had poor outcomes despite ruxolitinib, underscoring the need for novel therapies in this patient population. In conclusion the MCS is an accurate predictor of outcomes for patients who require second-line treatment and may be of use as an eligibility criterion for future clinical trials in this high-risk population.

Identifiers

PMID42523406
PMCPMC13405384

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.