Evidence map›Paper›PMID 40488928›Full record

ArticleDiscover oncology2025

Outcomes of secondary primary malignancies among patients with diffuse large B-cell lymphoma.

Peng Xu, Yan Lin, Weiying Gu, Zhenyu Li

Abstract read
In one paragraph

Article in Discover oncology, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Peng Xu *Key Laboratory of Bone Marrow Stem Cell, Blood Disease Institute, Xuzhou Medical University, Xuzhou, China.
Yan Lin *Department of Hematology, First People's Hospital of Changzhou, Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.
Weiying GuDepartment of Hematology, First People's Hospital of Changzhou, Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China. guweiying2001@163.com.
Zhenyu LiKey Laboratory of Bone Marrow Stem Cell, Blood Disease Institute, Xuzhou Medical University, Xuzhou, China. lizhenyumd@163.com.

Funding

This work was partially supported by the Key Projects of Jiangsu Provincial Health Commission . K2023028
6 · The paper itself

Abstract

backgroundAn increased risk of secondary primary malignancies (SPMs) has been shown in diffuse large B-cell lymphoma (DLBCL) patients after treatment. However, research on SPM outcomes in DLBCL patients is limited.

methodsUtilizing the population-based Surveillance, Epidemiology, and End Results Registry (SEER), the authors examined the characteristics, overall survival (OS), and treatments in DLBCL patients who developed secondary cancers of the breast, prostate, lung, colon/rectum, bladder cancers, melanoma, myeloma, and acute leukemia. Each patient was matched by age, sex, race, year of diagnosis, and stage to 50 controls from a general population diagnosed with a non-DLBCL primary the cancer.

resultsPatients with antecedent DLBCL who developed lung cancer (37.3% vs. 18.3%, P < 0.001) or colon/rectum cancer (45.5% vs. 39.6%, P = 0.032) were more commonly diagnosed at an early stage. Compared with patients in the control group, patients with antecedent DLBCL who developed prostate cancer, melanoma, myeloma, and acute leukemia had significantly worse OS. Conversely, patients who developed lung cancer after their antecedent DLBCL diagnosis showed markedly better OS. Amongst patients with antecedent DLBCL aged over 60, intensive therapy was associated with improved OS compared to supportive care in those being treated for a SPM diagnosis of breast, prostate, lung, colon/rectum, melanoma or bladder cancer, but not myeloma or acute leukemia. The rates of surgical resection were the same between patients with antecedent DLBCL and those in the control group, except for lower prostatectomy rates and higher lobectomy rates among patients with antecedent DLBCL.

conclusionsOur findings can assist clinicians in better understanding the survival outcomes of SPMs among patients with antecedent DLBCL while suggesting that long-term follow-up might be useful to detect DLBCL survivors who developed SPMs.

Indexed as

Diffuse large B-cell lymphomaEnd results registryEpidemiologySecondary primary malignanciesSurveillanceSurvival outcomes

Identifiers

PMID40488928
PMCPMC12149349

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