Evidence map›Paper›PMID 40823316›Full record

ArticleHemaSphere2025

Autologous stem cell transplantation in NK/T-cell lymphoma: Prognostic impact of EBV-DNA in a multinational cohort-A study by the EBMT Lymphoma Working Party.

Philipp Berning, Maud Ngoya, Won Seog Kim, Evgenii Shumilov, Depei Wu, Haiwen Huang, Anne Cairoli, Alessandra Tucci, Guillaume Dachy, Romain Gounot and 18 more

Abstract read
In one paragraph

Article in HemaSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

28 authors.

Philipp BerningDepartment of Medicine A, Hematology, Oncology and Pneumology University Hospital Muenster Muenster Germany.ORCID https://orcid.org/0000-0003-0442-3521
Maud NgoyaEuropean Society for Blood and Marrow Transplantation Paris France.
Won Seog KimSungkyunkwan University School of Medicine, Samsung Medical Center Seoul South Korea.
Evgenii ShumilovDepartment of Medicine A, Hematology, Oncology and Pneumology University Hospital Muenster Muenster Germany.ORCID https://orcid.org/0000-0003-0178-1729
Depei WuNational Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology The First Affiliated Hospital of Soochow University Suzhou China.
Haiwen HuangNational Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology The First Affiliated Hospital of Soochow University Suzhou China.ORCID https://orcid.org/0000-0002-1824-5247
Anne CairoliDivision of Haematology, Department of Oncology University Hospital of Lausanne (CHUV) Lausanne Switzerland.
Alessandra TucciDepartment of Hematology ASST Spedali Civili Brescia Italy.
Guillaume DachyHematology Department Cliniques Universitaires Saint-Luc Brussels Belgium.
Romain GounotService Hématologie Hôpital Henri Mondor Creteil France.
Anne C WilkeUniversity Hospital Frankfurt, Goethe University Frankfurt Main Germany.
Christof ScheidDepartment I of Internal Medicine, Medical Faculty and University Hospital of Cologne University of Cologne Cologne Germany.
Peter DregerDepartment of Medicine V University of Heidelberg Heidelberg Germany.
Jose Luis Lopez LorenzoHematology Department Hospital Universitario Fundación Jiménez Díaz UAM Madrid Spain.
Adrian BloorChristie Hospital NHS Foundation Trust Manchester UK.
Joanna Romejko-JarosinskaDepartment of Lymphoid Malignancies Maria Sklodowska-Curie National Research Institute of Oncology Warsaw Poland.
Alain GadisseurDepartment of Hematology University Medical Center Antwerpen Edegem Belgium.
Roland SchroersMedizinische Klinik II, Knappschaft Kliniken Universitätsklinikum Bochum Bochum Germany.
Péter ReményiDél-pesti Centrumkórház-Országos Hematológiai és Infektológiai Intézet, Dept. Haematology and Stem Cell Transplant Budapest Hungary.
Ludovic GabellierHematology Department University Hospital of Montpellier Montpellier France.
Monica PoianiUCO Ematologia, Azienda Sanitaria Universitaria Giuliano Isontina Trieste Italy.
Khalid HalahlehKing Hussein Cancer Centre Adult BMT Program Amman Jordan.
Jacques-Emmanuel GalimardEuropean Society for Blood and Marrow Transplantation Paris France.
Georg LenzDepartment of Medicine A, Hematology, Oncology and Pneumology University Hospital Muenster Muenster Germany.
Anna SuredaHematology Department Institut Català d'Oncologia Hospitalet, IDIBELL, Universitat de Barcelona Barcelona Spain.
Ali BazarbachiDepartment of Internal Medicine American University of Beirut Medical Center, Hematology-Oncology Division Beirut Lebanon.ORCID https://orcid.org/0000-0002-7171-4997
Bertram GlassDepartment of Hematology and Stem Cell Transplantation Helios Clinic Berlin-Buch Germany.
Norbert SchmitzDepartment of Medicine A, Hematology, Oncology and Pneumology University Hospital Muenster Muenster Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK)/T-cell lymphomas (NKTCLs) are rare, aggressive lymphomas prevalent in East Asia and South America. Despite improvements, largely due to asparaginase-based therapies, outcomes for advanced disease remain poor, and the role of autologous stem cell transplantation (auto-HCT) remains controversial. This study evaluated real-world outcomes of auto-HCT in NKTCL patients across Asia and Europe. We included 130 adult NKTCL patients undergoing auto-HCT between 2011 and 2022 using data from the European Society for Blood and Marrow Transplantation (EBMT) registry and South Korean registry data. Median age was 51.3 years; 66.9% were male. Most patients (95.1%) had an Eastern Cooperative Oncology Group (ECOG) score 0-1; 65.3% had Stage III-IV disease. One prior therapy line was reported in 53.1%, and ≥2 lines in 46.9%. Asparaginase-based regimens were used in 79.5% pretransplant. Responses at auto-HCT included complete (59.7%), partial (27.9%) remission, and stable/progressive disease (12.4%). Epstein-Barr virus (EBV)-DNA in the peripheral blood was reported in 37.3%. With a median follow-up of 4.6 years, 3-year overall survival (OS) and progression-free survival (PFS) were 63.8% and 47.6%. Relapse and NRM rates at 3 years were 46.7% and 5.7%. Patients in complete remission had improved 3-year OS (75.2%) compared to PR (52.8%) and stable/progressive disease (32.0%) (P = 0.007). Detectable EBV-DNA in the blood at auto-HCT was associated with poor outcomes (3-year OS: 26.7% vs. 78.1% in patients with undetectable EBV-DNA; P < 0.0001). Patients achieving complete remission and undetectable EBV-DNA in the blood before auto-HCT had a favorable survival, suggesting auto-HCT may be a treatment option in selected high-risk patients. This is the largest multinational cohort evaluating prognostic factors for auto-HCT for NKTCL.

Identifiers

PMID40823316
PMCPMC12355192

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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.