Evidence map›Paper›PMID 33966293›Full record

ArticleEuropean journal of haematology2021

Cumulative exposure to melphalan chemotherapy and subsequent risk of developing acute myeloid leukemia and myelodysplastic syndromes in patients with multiple myeloma.

Gudbjorg Jonsdottir, Magnus Björkholm, Ingemar Turesson, Malin Hultcrantz, Benjamin Diamond, Anna Porwit, Ola Landgren, Sigurdur Y Kristinsson

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in European journal of haematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 6 institutions in 3 countries.

Gudbjorg JonsdottirFaculty of Medicine, University of Iceland, Reykjavik, Iceland.ORCID https://orcid.org/0000-0002-8958-6022
Magnus BjörkholmDepartment of Medicine, Division of Hematology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Ingemar TuressonDepartment of Hematology, Skåne University Hospital, Malmö, Sweden.ORCID https://orcid.org/0000-0002-4115-8010
Malin HultcrantzDepartment of Medicine, Division of Hematology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Benjamin DiamondMyeloma Service, Memorial Sloan-Kettering Center, New York, NY, USA.
Anna PorwitDivision of Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Ola LandgrenMyeloma Program, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA.
Sigurdur Y KristinssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.ORCID https://orcid.org/0000-0002-4964-7476
Karolinska University Hospital · SEMemorial Sloan Kettering Cancer Center · USLund University · SESkåne University Hospital · SEUniversity of Iceland · ISUniversity of Miami · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI George S. Grills · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

objectivesThe aim of this study was to determine risk factors for development of acute myeloid leukemia/myelodysplastic syndromes (AML/MDS) in patients with multiple myeloma (MM).

methodsWe identified all patients diagnosed with MM in Sweden from January 1st, 1958 to December 31, 2011. A total of 26 627 patients were diagnosed with MM with during the study period. Of these, 124 patients (0.5%) developed subsequent AML/MDS. For each patient with MM and a subsequent AML/MDS diagnosis, we randomly selected a matched (age, sex, and date of MM diagnosis) MM patient without a subsequent second malignancy diagnosis.

resultsThe cumulative melphalan exposure was significantly higher (OR = 2.8, 95% CI 1.7-5.2; P < .001) among cases (median 988 mg; IQR 644-1640) compared with controls (median 578 mg; IQR 360-967). Median time to AML/MDS development was 3.8 years (IQR 2.8-5.8). Risk of AML/MDS was not statistically altered by M protein isotype, anemia, renal failure, hypercalcemia, lytic bone lesions, or radiation therapy.

conclusionIn this nationwide population-based study, we show that increased cumulative doses of alkylating therapy with melphalan increases the subsequent risk of developing AML/MDS in patients with MM. Given improved survival in MM patients over the last decade future studies will be important to better define long-term risks.

Indexed as

Antineoplastic Agents, AlkylatingDisease SusceptibilityHumansLeukemia, Myeloid, AcuteMelphalanMultiple MyelomaMyelodysplastic SyndromesNeoplasms, Second PrimaryPublic Health SurveillanceRisk AssessmentRisk FactorsSwedenAntineoplastic Agents, AlkylatingMelphalanacute myeloid leukemia/myelodysplastic syndromesalkylating therapymelphalanmultiple myelomasecond malignancies

Identifiers

PMID33966293
PMCPMC11036135
OpenAlexW3160658638

What OpenQuestion holds

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Registered trials

None linked

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.