Evidence map›Paper›PMID 42856879›Full record

ArticleFrontiers in oncology2026

Allogeneic hematopoietic cell transplantation for therapy-related hematological malignancies in patients with multiple myeloma.

Markus Maulhardt, Alexander Casimir Angleitner, Judith Büntzel, Gina Westhofen, Margarete Elisabeth Laage, Justin Hasenkamp, Detlef Thomas Haase, Hannes Treiber, Enver Aydilek, Anna Lena Illert and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 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

12 authors.

Markus MaulhardtDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Alexander Casimir AngleitnerDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Judith BüntzelDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Gina WesthofenDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Margarete Elisabeth LaageDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Justin HasenkampDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Detlef Thomas HaaseDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Hannes TreiberDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Enver AydilekDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Anna Lena IllertDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Wolfram JungDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.
Gerald Georg WulfDepartment of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Improved survival in multiple myeloma (MM) patients after high-dose chemotherapy, autologous hematopoietic cell transplantation (auto-HCT), and novel agents has led to an increasing incidence of therapy-related hematological malignancies (t-HM), although optimal management remains unclear, particularly the role of allogeneic HCT (allo-HCT). We conducted a retrospective single-center study of adult MM patients who underwent first auto-HCT between 2010 and 2025 and subsequently developed t-HM, analyzing clinical, molecular, cytogenetic features, treatment strategies, and outcomes, with a focus on allo-HCT. Among 519 patients, 23 (4.4%) developed t-HM, including therapy-related acute myeloid leukemia (43%), myelodysplastic syndrome (35%), and B-cell acute lymphoblastic leukemia (17%), with a median latency of 58.7 months after auto-HCT. High-risk genetics were common, including

Indexed as

acute leukemiaallo-HCTauto-HCTmultiple myelomasecondary malignanciestherapy-related hematological malignancies

Identifiers

PMID42856879
PMCPMC13649491

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