Late-Onset Immune Checkpoint Inhibitor-Associated Nephrotoxicity and Suspected Thrombotic Microangiopathy Following Durvalumab Administration with a Challenging Clinical Course: A Case Report

A man in his 60s was diagnosed with distal cholangiocarcinoma after presenting to a local clinic with back pain and weight loss. Gemcitabine plus cisplatin therapy was initiated, and durvalumab was added 10 months later. The patient received 10 cycles of induction therapy after which follow-up contrast-enhanced computed tomography revealed disease progression, prompting the substitution of gemcitabine monotherapy for the original treatment regimen. Following 17 cycles of gemcitabine, the patient developed bilateral lower extremity edema and worsening renal function, leading to hospitalization. Laboratory tests revealed elevated serum creatinine levels, increased tubular injury markers and microscopic hematuria. Based on these findings, the patient’s history of immune checkpoint inhibitor administration, and after excluding other differential diagnoses, our provisional diagnosis was late-onset durvalumab-associated renal injury. Ultrasonography revealed deep vein thrombosis, prompting the initiation of anticoagulant therapy with rivaroxaban. As renal biopsy was contraindicated, empirical steroid therapy was initiated. This initially resulted in decreased serum concentrations of creatinine, N-acetyl-β-D-glucosaminidase, and β2-microglobulin. However, serum creatinine and β2-microglobulin levels subsequently increased, accompanied by a sudden and marked decrease in platelet count, indicating gemcitabine-induced thrombotic microangiopathy. To the best of our knowledge, this is the first reported case of coexisting late-onset immune checkpoint inhibitor-related nephrotoxicity and gemcitabine-induced thrombotic microangiopathy, the latter being strongly suspected based on the prevention of rapid renal function deterioration by steroid therapy. Steroid monotherapy was insufficient to achieve full renal recovery from thrombotic microangiopathy, highlighting the need for early recognition and timely intervention when administering gemcitabine to patients with a history of immune checkpoint inhibitor therapy.

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Journal
Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences)
Published
2026-02-09
DOI
https://doi.org/10.5649/jjphcs.52.93
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
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article

Late-Onset Immune Checkpoint Inhibitor-Associated Nephrotoxicity and Suspected Thrombotic Microangiopathy Following Durvalumab Administration with a Challenging Clinical Course: A Case Report

Sho Hasegawa, Midori Taguchi, Daisuke Umezu, Katsuhito Teramatsu et al.
Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences)
Cancer Immunotherapy and Biomarkers
article

Late-Onset Immune Checkpoint Inhibitor-Associated Nephrotoxicity and Suspected Thrombotic Microangiopathy Following Durvalumab Administration with a Challenging Clinical Course: A Case Report

Sho Hasegawa, Midori Taguchi, Daisuke Umezu, Katsuhito Teramatsu, Kazuaki Usui, Mayu Kondo, Risa Hashimoto, Hideki Kimoto
article en

Abstract

A man in his 60s was diagnosed with distal cholangiocarcinoma after presenting to a local clinic with back pain and weight loss. Gemcitabine plus cisplatin therapy was initiated, and durvalumab was added 10 months later. The patient received 10 cycles of induction therapy after which follow-up contrast-enhanced computed tomography revealed disease progression, prompting the substitution of gemcitabine monotherapy for the original treatment regimen. Following 17 cycles of gemcitabine, the patient developed bilateral lower extremity edema and worsening renal function, leading to hospitalization. Laboratory tests revealed elevated serum creatinine levels, increased tubular injury markers and microscopic hematuria. Based on these findings, the patient’s history of immune checkpoint inhibitor administration, and after excluding other differential diagnoses, our provisional diagnosis was late-onset durvalumab-associated renal injury. Ultrasonography revealed deep vein thrombosis, prompting the initiation of anticoagulant therapy with rivaroxaban. As renal biopsy was contraindicated, empirical steroid therapy was initiated. This initially resulted in decreased serum concentrations of creatinine, N-acetyl-β-D-glucosaminidase, and β2-microglobulin. However, serum creatinine and β2-microglobulin levels subsequently increased, accompanied by a sudden and marked decrease in platelet count, indicating gemcitabine-induced thrombotic microangiopathy. To the best of our knowledge, this is the first reported case of coexisting late-onset immune checkpoint inhibitor-related nephrotoxicity and gemcitabine-induced thrombotic microangiopathy, the latter being strongly suspected based on the prevention of rapid renal function deterioration by steroid therapy. Steroid monotherapy was insufficient to achieve full renal recovery from thrombotic microangiopathy, highlighting the need for early recognition and timely intervention when administering gemcitabine to patients with a history of immune checkpoint inhibitor therapy.

Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences)Vol. 52(2)
Kyushu Rosai Hospital (JP), Japan Organization of Occupational Health and Safety (JP)
Good health and well-being
Openalex Percentile: Top 61%
Cancer Immunotherapy and Biomarkers
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