Population-based study reveals increased risk factors for secondary myeloid neoplasms in patients with hematologic cancers, indicating critical implications for survivorship.
As survival rates for lymphoid malignancies continue to improve, understanding the late effects post-treatment, such as secondary myeloid neoplasms (sMN), is increasingly critical for survivorship. This large-scale population-based (SEER-Medicare) study investigated risk factors and cumulative incidence of sMN in patients with diagnosis of diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), and multiple myeloma (MM) between 2000 and 2011, with follow-up through 2015. FL patients had a continuous increase in the cumulative incidence in sMN with longer follow-up, while MM patients incidence plateaued after 60 months. Notably, DLBCL patients diagnosed in more recent years (2004-2007 and 2008-2011) had a higher cumulative sMN incidence compared to those diagnosed earlier (2000-2003). In the Medicare population, older age at diagnosis was associated with significant increase in sMN risk in DLBCL and FL patients. Chemotherapy exposure, or granulocyte-colony stimulating factor (G-CSF) exposure significantly increased sMN risk across all three malignancies. Chronic autoimmune conditions increased sMN risk in DLBCL patients. These findings provide crucial insights into sMN risk factors. Chemotherapy exposure is a recognized risk factor, comorbidities such as a history of autoimmunity and G-CSF exposures have been identified as additional mediators of sMN risk in our study.
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Singh et al. (2025) studied this question.
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