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March 27, 2026JNCI Journal of the National Cancer Institute2 citations

Cardiovascular disease risk after radiotherapy and anthracycline-based chemotherapy for diffuse large B-cell lymphoma

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YGY.M. GeurtsRadboud University NijmegenSNSuzanne I.M. NeppelenbroekOncode InstituteBABerthe M P AlemanThe Netherlands Cancer Institute

Key Result

Diffuse large B-cell lymphoma survivors face a 3.9-fold higher heart failure risk than the general population, with >300 mg/m2 doxorubicin increasing cardiomyopathy risk 2.8-fold.

Key Points

  • To examine long-term cardiovascular disease risks in diffuse large B-cell lymphoma survivors treated with potentially cardiotoxic therapies.
  • Analyzed a multicenter cohort of 2,356 DLBCL survivors over a median follow-up of 14.2 years.
  • Collected cardiovascular disease data from medical records and disease registries.
  • Calculated standardized incidence ratios and absolute excess risks for comparison with the general population.
  • Utilized multivariable Cox regression to assess treatment-specific cardiovascular risks.
  • 312 survivors diagnosed with cardiovascular disease after five years post-treatment.
  • Increased heart failure risk (SIR 3.9) and cerebrovascular accident risk (SIR 1.3) compared to the general population.
  • Decreased coronary artery disease risk (SIR 0.7) in DLBCL survivors.
  • Higher heart failure risk among females (SIR 5.3) and younger survivors (SIR 10.5) at treatment.
  • High exposure to doxorubicin showed a 2.8-fold increased risk of cardiomyopathy/heart failure.

Structured PICO

Does radiotherapy and anthracycline-based chemotherapy increase the risk of cardiovascular diseases in DLBCL survivors compared to the general population?

P
Population
≥ 5-year diffuse large B-cell lymphoma (DLBCL) survivors treated at ages 15 to 61 years in 1989 to 2012
I
Intervention
Radiotherapy and/or anthracycline-based chemotherapy with/without rituximab
C
Comparator
Expected CVD-incidence in the Dutch general population
O
Outcome
First cardiovascular disease (CVD) ≥5 years after treatmenthard clinical

DLBCL survivors treated with anthracyclines and radiotherapy face a significantly elevated long-term risk of heart failure, particularly females and those treated at younger ages, warranting individualized cardiac screening.

Abstract

Abstract Background Few studies examined treatment-specific long-term risks of cardiovascular diseases (CVD) in diffuse large B-cell lymphoma (DLBCL) survivors treated with potentially cardiotoxic radiotherapy and/or chemotherapy with/without rituximab after the 1990s. Methods Long-term CVD risk was examined in a multicenter cohort comprising 2,356 ≥ 5-year DLBCL survivors treated at ages 15 to 61 years in 1989 to 2012. CVD data were acquired from medical records, general practitioners and disease-registries. Observed CVD-numbers were compared with expected CVD-incidence in the Dutch population to estimate standardized incidence ratios (SIRs) and absolute excess risks (AERs/10,000 person-years). Treatment-specific CVD risks were assessed using multivariable Cox regression. Results During a median follow-up of 14.2 years (IQR 10.1 to 18.9), 312 survivors were diagnosed with a first CVD ≥5 years after treatment. Compared with the general population, DLBCL survivors had increased risks of heart failure (HF, SIR 3.9, 95%CI 3.4-4.6, AER 62.8) and cerebrovascular accident (SIR 1.3, 95%CI 1.0 to 1.7, AER 9.8), while risk of coronary artery disease was decreased (SIR 0.7, 95%CI 0.5-0.9, AER -30.9). HF risk was higher among females (SIR 5.3, 95%CI 4.2 to 6.5) than males (SIR 3.2, 95%CI 2.6-4.0, P heterogeneity0.001), and among survivors ≤40 years at DLBCL treatment (SIR 10.5, 95%CI 7.2 to 14.8, P trend0.001). Exposure to 300 mg/m2 doxorubicin was associated with a 2.8-fold (95%CI 1.7-4.5) increased risk of cardiomyopathy/HF, while radiotherapy involving the heart was associated with a 1.9-fold (95%CI 1.1 to 3.1) increased risk of valvular heart disease. Conclusion ≥5-year DLBCL survivors have increased risks of developing CVDs, especially HF. Physicians and patients should recognize this risk, and individualized cardiac screening should be considered.

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Cite This Study

Geurts et al. (2026) studied this question. Diffuse large B-cell lymphoma survivors face a 3.9-fold higher heart failure risk than the general population, with >300 mg/m2 doxorubicin increasing cardiomyopathy risk 2.8-fold.

synapsesocial.com/papers/69c6201515a0a509bde18773https://doi.org/10.1093/jnci/djag085
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