Evidence map›Paper›PMID 40334055›Full record

SynthesisCancer2025

Allogeneic versus autologous stem cell transplantation after relapsing following first line autologous transplantation for multiple myeloma: A systematic review.

Heinz Ludwig, Sarah Bernhard, Takashi Ikeda, Cesar O Freytes, Martin Schreder, Koji Kawamura, Yoshiko Atsuta, Hiroyuki Takamatsu, David H Vesole, Parameswaran Hari and 2 more

Abstract readSystematic ReviewComparative StudyMeta-Analysis
In one paragraph

Synthesis in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Heinz LudwigWilhelminen Cancer Research Institute, Vienna, Austria.ORCID https://orcid.org/0000-0002-3302-8726
Sarah BernhardWilhelminen Cancer Research Institute, Vienna, Austria.
Takashi IkedaDivision of Hematology and Stem Cell Transplantation, Shizuoka Cancer Center, Shizuoka, Japan.
Cesar O FreytesUniversity of Texas Health Science Center San Antonio, San Antonio, Texas, USA.
Martin SchrederDepartment of Medicine I, Center for Oncology and Hematology, Clinic Ottakring, Vienna, Austria.
Koji KawamuraHematology, Tottori University Hospital, Yonago, Japan.
Yoshiko AtsutaJapanese Data Center For Hematopoietic Cell Transplantation, Nagakute, Japan.
Hiroyuki TakamatsuKanazawa University, Kanazawa, Ishikawa, Japan.ORCID https://orcid.org/0000-0001-9515-0017
David H VesoleMyeloma Division, John Theurer Cancer Center, Hackensack Meridian School of Medicine, Hackensack, New Jersey, USA.
Parameswaran HariDepartment of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Julie KrainerWilhelminen Cancer Research Institute, Vienna, Austria.
Axel HinkeCancer Clinical Research Consulting, Düsseldorf, Germany.

Funding

Austrian Forum Against Cancer
6 · The paper itself

Abstract

backgroundAllogeneic stem cell transplantation (allo-SCT) has curative potential and was previously considered by several experts superior to autologous stem cell transplantation (auto-SCT) for patients with multiple myeloma relapsing after first-line auto-SCT.

methodsThe authors conducted a comprehensive literature review of English-language studies published from 1995 to October 2024. Five studies comparing allo-SCT with second auto-SCT following first line auto-SCT in multiple myeloma were included. Two additional studies comparing patients with or without a suitable allo-SCT donor after relapse were analyzed separately. Individual data from 815 patients were obtained from two large databases: the Japan Society for Hematopoietic Stem Cell Transplantation and the Center for International Blood & Marrow Transplant Research (CIBMTR). Data from five smaller studies (three comparing allo-vs. auto-SCT and two comparing donor vs. no-donor groups) presented via Kaplan-Meier curves were digitized using the Shiny app. Meta-analyses were performed using R 4.3.3. Kaplan-Meier and log-rank tests for overall survival (OS) and progression-free survival (PFS) were conducted in SPSS.

resultsIndividual patient data analysis showed significantly longer OS in the auto-SCT group. This benefit was consistent in the three smaller studies. PFS was also superior for auto-SCT in the CIBMTR data set and the pooled smaller studies. In the two-donor vs. no-donor studies, the donor group showed better PFS, with OS also improved when data were combined.

conclusionsAllo-SCT after relapse from first line auto-SCT resulted in inferior OS and PFS compared to a second auto-SCT. These findings indicate that allo-SCT should no longer be recommended in patients with multiple myeloma relapsing after first line auto-SCT.

Indexed as

Hematopoietic Stem Cell TransplantationMultiple MyelomaNeoplasm Recurrence, LocalHumansRecurrenceTransplantation, AutologousTransplantation, Homologousallogeneic stem cell transplantationautologous stem cell transplantationmultiple myelomarelapsed/refractory myelomasecond‐line therapy

Identifiers

PMID40334055
PMCPMC12057802

What OpenQuestion holds

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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.