Red cell distribution width: a novel and accessible predictor for immune checkpoint inhibitor-associated myocarditis—a retrospective cohort study - Summary - MDSpire

Red cell distribution width: a novel and accessible predictor for immune checkpoint inhibitor-associated myocarditis—a retrospective cohort study

  • By

  • Shili Zhong

  • Hao Zhang

  • Meicong Zhao

  • Zhu Yuan

  • Zhen Wang

  • Zhengbin Wu

  • June 26, 2026

  • 0 min

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Objective:

To investigate the role of red blood cell distribution width (RDW) in immune checkpoint inhibitor (ICI)-associated myocarditis and its potential as a diagnostic indicator.

Approach:
  • Study Design: A single-center retrospective study was conducted from January 2020 to January 2024, including 51 patients with PD-1 inhibitor-associated myocarditis, 58 patients with viral myocarditis, and 50 anti-PD-1-treated patients without myocarditis.
  • Data Analysis: Clinical and laboratory data, including RDW and troponin T (TnT), were analyzed using statistical tests such as one-way ANOVA and ROC curve analysis.
Key Findings:
  • RDW was significantly elevated in the ICI-associated myocarditis group compared to both control groups (P < 0.05).
  • Multivariate logistic regression identified RDW (OR = 3.78) and ln(TnT) (OR = 12.12) as independent factors associated with ICI-associated myocarditis (P < 0.05).
  • ROC analysis showed RDW had an AUC of 0.8882 (cut-off = 14.65; sensitivity 85.6%, specificity 90.5%), comparable to TnT (AUC = 0.9102).
  • The mean onset time after PD-1 inhibition therapy was 153.5 ± 184.5 days, and the mean hospitalization period was 13.6 ± 17.5 days.
Interpretation:

Limitations:
  • The study is retrospective and conducted at a single center, which may limit generalizability.
  • The diagnostic criteria for ICI-associated myocarditis are not standardized, leading to potential subjectivity in diagnosis.
Conclusion:

RDW may serve as a practical, noninvasive, complementary auxiliary indicator for early screening and risk stratification of ICI-associated myocarditis.

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