Evidence map›Paper›PMID 41236718›Full record

ArticleCancer research communications2025

Risk Factors beyond Chemotherapy Exposure for Secondary Myeloid Neoplasms after Hematologic Cancers: A SEER-Based Study.

Abhay Singh, Theresa Hahn, Rahul Mishra, Megan M Herr, Swapna Thota

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Abhay SinghDepartment of Hematology Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0001-6657-8647
Theresa HahnDepartment of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-3835-8855
Rahul MishraDepartment of Internal Medicine, Anne Arundel Medical Center, Annapolis, Maryland.ORCID 0000-0001-5631-1164
Megan M HerrDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0001-5768-9396
Swapna ThotaDivision of Hematology/Oncology, University of Tennessee Health Science Center, Memphis, Tennessee.ORCID 0000-0002-4216-1414

Funding

NCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS HHSN261201800032CNCI NIH HHS HHSN261201800032I
6 · The paper itself

Abstract

As survival rates for lymphoid malignancies continue to improve, understanding the late effects after treatment, such as secondary myeloid neoplasms (sMN), is increasingly critical for survivorship. This large-scale population-based (SEER-Medicare) study investigated the risk factors and cumulative incidence of sMNs in patients with diagnosis of diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), and multiple myeloma between 2000 and 2011, with follow-up through 2015. Patients with FL had a continuous increase in the cumulative incidence of sMNs with longer follow-up, whereas incidence of patients with multiple myeloma plateaued after 60 months. Notably, patients with DLBCL diagnosed in more recent years (2004-2007 and 2008-2011) had a higher cumulative sMN incidence compared with those diagnosed earlier (2000-2003). In the Medicare population, older age at diagnosis was associated with significant increase in sMN risk in patients with DLBCL and FL. Chemotherapy exposure or G-CSF exposure significantly increased sMN risk across all three malignancies. Chronic autoimmune conditions increased sMN risk in patients with DLBCL. These findings provide crucial insights into sMN risk factors. Chemotherapy exposure is a recognized risk factor, and comorbidities such as a history of autoimmunity and G-CSF exposures have been identified as additional mediators of sMN risk in our study. SIGNIFICANCE: Our study reveals population-level risk factors for sMNs, including novel links to autoimmune disease and G-CSF, in addition to known causes like chemotherapy/radiation. These findings underscore the complex pathogenesis of sMNs and the need for molecular data in prospective studies to guide prevention, detection, and survivorship care.

Indexed as

Bone Marrow NeoplasmsHematologic NeoplasmsNeoplasms, Second PrimaryAgedAged, 80 and overAntineoplastic AgentsAutoimmune DiseasesCancer SurvivorsComorbidityFemaleFollow-Up StudiesGranulocyte Colony-Stimulating FactorHumansIncidenceLymphoma, FollicularLymphoma, Large B-Cell, DiffuseAntineoplastic AgentsGranulocyte Colony-Stimulating Factor

Identifiers

PMID41236718
PMCPMC12696405

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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.