Evidence map›Paper›PMID 40275355›Full record

ArticleJournal of hematology & oncology2025

PFS24 as a prognostic milestone in patients with newly diagnosed primary CNS lymphoma.

Vanja Zeremski, Tobias R Haage, Hanno M Witte, Louisa Adolph, Sina A Beer, Gerhard Behre, Benedikt Jacobs, Christoph Kahl, Chrysavgi Lalayanni, Jens Panse and 8 more

Abstract readLetterMulticenter Study
In one paragraph

Article in Journal of hematology & oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

18 authors.

Vanja ZeremskiDepartment of Hematology, Oncology and Cell Therapy, Medical Faculty, Otto von Guericke University Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany. vanja.zeremski@med.ovgu.de.
Tobias R HaageDepartment of Hematology, Oncology and Cell Therapy, Medical Faculty, Otto von Guericke University Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany.
Hanno M WitteDepartment of Hematology and Oncology, Federal Armed Forces Hospital Ulm, Ulm, Germany.
Louisa AdolphDepartment of Internal Medicine III, Ludwig-Maximilians-University Hospital, Munich, Germany.
Sina A BeerDepartment of Hematology and Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Gerhard BehreDessau Medical Center, Clinic for Internal Medicine I- Gastroenterology, Hematology, Oncology, Hemostaseology, Palliative Medicine, Infectious Diseases, Pneumology, Nephrology, Dessau-Rosslau, Germany.
Benedikt JacobsDepartment of Internal Medicine 5, Hematology and Clinical Oncology, Friedrich-Alexander- Universität Erlangen-Nürnberg (FAU), University Hospital Erlangen, Erlangen, Germany.
Christoph KahlDepartment of Hematology, Oncology and Palliative Care, Klinikum Magdeburg, Magdeburg, Germany.
Chrysavgi LalayanniBone Marrow Transplantation Unit, Hematology Department, G. Papanicolaou Hospital, Thessaloniki, Greece.
Jens PanseDepartment of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Sotirios PapageorgiouSecond Department of Internal Medicine and Research Institute, Athens University Medical School, Attikon University General Hospital, Athens, Greece.
Marina P SiakantarisDepartment of Hematology and Bone Marrow Transplantation Unit, National and Kapodistrian University of Athens, Laiko General Hospital, Athens, Greece.
Jessica SchneiderDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Ulf SchnetzkeDepartment of Internal Medicine II, Hematology and Medical Oncology, University Hospital Jena, Jena, Germany.
Alexander SchulzDessau Medical Center, Clinic for Internal Medicine I- Gastroenterology, Hematology, Oncology, Hemostaseology, Palliative Medicine, Infectious Diseases, Pneumology, Nephrology, Dessau-Rosslau, Germany.
Theodoros P VassilakopoulosDepartment of Hematology and Bone Marrow Transplantation Unit, National and Kapodistrian University of Athens, Laiko General Hospital, Athens, Greece.
Jeanette WalterDepartment of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Dimitrios MougiakakosDepartment of Hematology, Oncology and Cell Therapy, Medical Faculty, Otto von Guericke University Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-dose chemotherapy followed by autologous hematopoietic stem cell transplantation has significantly improved overall survival (OS) in primary central nervous system lymphoma (PCNSL). However, early identification of long-term survivors remains a challenge. Progression-free survival at 24 months (PFS24) has emerged as a key prognostic marker in diffuse large B-cell lymphoma, but its relevance in PCNSL is still unclear. In this retrospective multicenter study, we analyzed data from 146 newly diagnosed, transplant-eligible PCNSL patients treated with MATRix-like regimens across 14 hospitals. With a median follow-up of 48 months, the 2-year PFS and OS rates were 50.4% and 65.6%, respectively. Of the 139 patients evaluable for PFS24-analysis, 51.1% reached PFS24, with a subsequent 5-year OS of 96.7%. Of note, the annual hazard rate for progression and death decreased to under 5% after 24 months, remaining stable thereafter. The patients who failed to reach PFS24 had a median OS of only 6.0 months. Key predictors of PFS failure included impaired Karnofsky performance status and treatment dose-reduction. In conclusion, PFS24 was identified as an important prognostic marker in PCNSL. Patients who achieve PFS24 have a favorable prognosis, whereas those who do not face poor outcomes and require innovative treatment approaches. This insight could aid in risk stratification and support the use of PFS24 as a surrogate endpoint in clinical trials.

Indexed as

Central Nervous System NeoplasmsLymphomaAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedPrognosisProgression-Free SurvivalRetrospective StudiesYoung AdultOverall survivalPFS24Primary CNS lymphoma

Identifiers

PMID40275355
PMCPMC12023625

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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 OpenQuestion graph.