Immune checkpoint inhibitor-related myocarditis during DUO-E regimen for endometrial cancer: The first case report in gynecologic oncology.
[BACKGROUND] Immune checkpoint inhibitors (ICIs) are increasingly used in gynecologic oncology, with the DUO-E regimen-carboplatin, paclitaxel, and durvalumab-recently approved in Japan for advanced o
APA
Yamabe E, Yamamoto H, et al. (2025). Immune checkpoint inhibitor-related myocarditis during DUO-E regimen for endometrial cancer: The first case report in gynecologic oncology.. Gynecologic oncology reports, 61, 101924. https://doi.org/10.1016/j.gore.2025.101924
MLA
Yamabe E, et al.. "Immune checkpoint inhibitor-related myocarditis during DUO-E regimen for endometrial cancer: The first case report in gynecologic oncology.." Gynecologic oncology reports, vol. 61, 2025, pp. 101924.
PMID
41169954
Abstract
[BACKGROUND] Immune checkpoint inhibitors (ICIs) are increasingly used in gynecologic oncology, with the DUO-E regimen-carboplatin, paclitaxel, and durvalumab-recently approved in Japan for advanced or recurrent endometrial cancer. However, ICI-related myocarditis (ICI-M) is a rare but potentially fatal adverse event requiring prompt recognition and treatment.
[CASE PRESENTATION] A 74-year-old woman with advanced endometrial cancer developed ICI-M following four cycles of DUO-E therapy. Sixteen days post-treatment, she presented with fever and fatigue. Markedly elevated troponin I (39.8 ng/mL), new-onset complete right bundle branch block, and a reduced left ventricular ejection fraction (40 %) raised suspicion for ICI-M. Endomyocardial biopsy revealed diffuse CD8 + T-cell infiltration and myocyte necrosis, consistent with active myocarditis. High-dose methylprednisolone (1 g/day) was promptly initiated, resulting in rapid cardiac recovery and clinical stabilization. Chemotherapy was successfully resumed after steroid tapering.
[CONCLUSION] This is the first reported case of ICI-M during DUO-E therapy for endometrial cancer. It underscores the importance of early clinical suspicion, rapid multidisciplinary collaboration, and timely intervention in managing ICI-M, particularly in high-risk patients. Continuous vigilance is warranted throughout the course of ICI therapy.
[CASE PRESENTATION] A 74-year-old woman with advanced endometrial cancer developed ICI-M following four cycles of DUO-E therapy. Sixteen days post-treatment, she presented with fever and fatigue. Markedly elevated troponin I (39.8 ng/mL), new-onset complete right bundle branch block, and a reduced left ventricular ejection fraction (40 %) raised suspicion for ICI-M. Endomyocardial biopsy revealed diffuse CD8 + T-cell infiltration and myocyte necrosis, consistent with active myocarditis. High-dose methylprednisolone (1 g/day) was promptly initiated, resulting in rapid cardiac recovery and clinical stabilization. Chemotherapy was successfully resumed after steroid tapering.
[CONCLUSION] This is the first reported case of ICI-M during DUO-E therapy for endometrial cancer. It underscores the importance of early clinical suspicion, rapid multidisciplinary collaboration, and timely intervention in managing ICI-M, particularly in high-risk patients. Continuous vigilance is warranted throughout the course of ICI therapy.