Evidence map›Paper›PMID 42351369›Full record

ArticleBritish journal of haematology2026

Response-adapted consolidation and salvage strategies in secondary central nervous system lymphoma: Insights from a multicentre cohort.

Farina Eigendorff, Fabian Görke, Vanja Zeremski, Sophia Wollnitza, Evgenii Shumilov, Georg Lenz, Ellen Obstfelder, Inken Hilgendorf, Vladan Vučinić, Andreas Hochhaus and 1 more

Abstract readMulticenter Study
In one paragraph

Article in British journal of haematology, 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

11 authors.

Farina EigendorffKlinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Comprehensive Cancer Center Central Germany-Campus Jena, Universitätsklinikum Jena, Jena, Germany.ORCID https://orcid.org/0009-0008-2727-8850
Fabian GörkeKlinik und Poliklinik für Hämatologie, Zelltherapie, Hämostaseologie und Infektiologie, Comprehensive Cancer Center Central Germany-Campus Leipzig, Universitätsklinikum Leipzig, Leipzig, Germany.
Vanja ZeremskiKlinik für Hämatologie, Onkologie und Zelltherapie, Universitätsklinikum Magdeburg, Magdeburg, Germany.ORCID https://orcid.org/0000-0002-5254-9885
Sophia WollnitzaMedizinische Klinik A, Hämatologie, Hämostaseologie, Onkologie und Pneumologie, Universitätsklinikum Münster, Münster, Germany.
Evgenii ShumilovMedizinische Klinik A, Hämatologie, Hämostaseologie, Onkologie und Pneumologie, Universitätsklinikum Münster, Münster, Germany.ORCID https://orcid.org/0000-0003-0178-1729
Georg LenzMedizinische Klinik A, Hämatologie, Hämostaseologie, Onkologie und Pneumologie, Universitätsklinikum Münster, Münster, Germany.
Ellen ObstfelderKlinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Comprehensive Cancer Center Central Germany-Campus Jena, Universitätsklinikum Jena, Jena, Germany.
Inken HilgendorfKlinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Comprehensive Cancer Center Central Germany-Campus Jena, Universitätsklinikum Jena, Jena, Germany.
Vladan VučinićKlinik und Poliklinik für Hämatologie, Zelltherapie, Hämostaseologie und Infektiologie, Comprehensive Cancer Center Central Germany-Campus Leipzig, Universitätsklinikum Leipzig, Leipzig, Germany.
Andreas HochhausKlinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Comprehensive Cancer Center Central Germany-Campus Jena, Universitätsklinikum Jena, Jena, Germany.
Ulf SchnetzkeKlinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Comprehensive Cancer Center Central Germany-Campus Jena, Universitätsklinikum Jena, Jena, Germany.ORCID https://orcid.org/0000-0001-7455-8988

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Secondary central nervous system lymphoma (SCNSL) remains a rare but challenging manifestation of aggressive lymphomas, with limited prospective data to guide treatment decisions in the modern therapeutic era. We conducted a multicentre retrospective cohort study of 105 consecutively treated adult patients diagnosed with SCNSL between 2016 and 2024 across four German academic centres, capturing detailed treatment sequencing, response dynamics and outcome data. Median progression-free survival (PFS) was 7.62 months (95% CI 5.34-9.90), and median overall survival (OS) was 16.62 months (95% CI 5.91-27.33). Consolidation with high-dose chemotherapy and autologous haematopoietic stem cell transplantation (HDT-AHSCT) was associated with significantly improved OS and PFS in univariate and multivariate analyses. Achieving complete remission prior to HDT-AHSCT conferred with superior outcomes. In a small subset of patients with relapsed/refractory (rr) SCNSL, CD19-directed chimeric antigen receptor T-cell (CAR T) therapy showed favourable outcomes compared with non-transplant salvage therapy in exploratory univariate analysis (OS HR 0.28, 95% CI 0.08-0.94, p = 0.039; PFS HR 0.37, 95% CI 0.16-0.88, p = 0.025). In this contemporary multicentre real-world cohort, early response and consolidative HDT-AHSCT emerged as key determinants of durable disease control, while CAR T therapy may represent a salvage strategy for selected patients. These findings provide clinically relevant benchmarks to inform risk-adapted treatment sequencing in SCNSL.

Indexed as

Central Nervous System NeoplasmsConsolidation ChemotherapySalvage TherapyAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedRetrospective StudiesCAR T therapyhigh‐dose chemotherapyprognostic factorssecondary CNS lymphoma

Identifiers

PMID42351369
PMCPMC13461960

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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.