Evidence map›Paper›PMID 39409984›Full record

ArticleCancers2024

Gender-Specific Prognostic Impact of Treosulfan Levels in High-Dose Chemotherapy for Multiple Myeloma.

Alexander D Heini, Karin Kammermann, Ulrike Bacher, Barbara Jeker, Michael Hayoz, Yolanda Aebi, Carlo R Largiadèr, Henning Nilius, Thomas Pabst

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

9 authors.

Alexander D HeiniDepartment of Medical Oncology, University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.
Karin KammermannDepartment of Medical Oncology, University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.
Ulrike BacherDepartment of Hematology and Central Hematology Laboratory, University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.ORCID 0000-0001-8771-947X
Barbara JekerDepartment of Medical Oncology, University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.
Michael HayozCenter of Laboratory Medicine (ZLM), University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.
Yolanda AebiCenter of Laboratory Medicine (ZLM), University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.
Carlo R LargiadèrCenter of Laboratory Medicine (ZLM), University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.ORCID 0000-0002-0889-8922
Henning NiliusCenter of Laboratory Medicine (ZLM), University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.ORCID 0000-0002-1323-3116
Thomas PabstDepartment of Medical Oncology, University Hospital Inselspital and University of Bern, 3010 Bern, Switzerland.ORCID 0000-0002-6055-5257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe growing body of evidence around sexual and gender dimorphism in medicine, particularly in oncology, has highlighted differences in treatment response, outcomes, and side effects between males and females. Differences in drug metabolism, distribution, and elimination, influenced by factors like body composition and enzyme expression, contribute to these variations.

methodsWe retrospectively analyzed data of 112 multiple myeloma (MM) patients treated with first-line high-dose chemotherapy (HDCT) with treosulfan and melphalan (TreoMel) followed by autologous stem cell transplantation (ASCT) at a single academic center between January 2020 and August 2022. We assessed response rate, progression-free survival (PFS), overall survival (OS), and toxicities in relation to gender and treosulfan exposure.

resultsOur analysis revealed significant gender-specific differences in treosulfan exposure. Females had higher peak levels (343.8 vs. 309.0 mg/L,

conclusionOur study demonstrates that female patients undergoing TreoMel HDCT have higher treosulfan exposure than males and that females with higher levels are at increased risk for toxicity and adverse outcomes. These data suggest that higher treosulfan doses do not confer a benefit in terms of better outcomes for females. Therefore, exploring lower treosulfan doses for female MM patients undergoing TreoMel HDCT may be warranted to mitigate toxicity and improve outcomes.

Indexed as

autologous stem cell transplantation (ASCT)gender differencehigh-dose chemotherapy (HDCT)myelomapharmacokineticstreosulfan

Identifiers

PMID39409984
PMCPMC11475554

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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.