ArticleESMO real world data and digital oncology2026
Subsequent systemic therapy initiation after first-line discontinuation in metastatic renal cell carcinoma: insights from a Japanese real-world cohort.
Article in ESMO real world data and digital oncology, 2026. 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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Abstract
Background: Sequential systemic therapy after first-line discontinuation in metastatic renal cell carcinoma remains incompletely characterized in routine practice. We aimed to evaluate subsequent systemic therapy initiation in a Japanese real-world cohort and identify clinical factors associated with failure to initiate subsequent therapy. Patients and methods: The primary analysis used real-world data from the Japanese AGEHA database ( Results: Among patients with PD- or AE-related discontinuation, subsequent systemic therapy was initiated in 66.7% of those receiving first-line tyrosine kinase inhibitor (TKI) monotherapy and 59.9% of those receiving immune-oncology (IO)-based regimens. Failure to initiate subsequent therapy was independently associated with poorer Eastern Cooperative Oncology Group performance status and receipt of IO-based first-line regimens, whereas discontinuation due to PD was associated with a higher likelihood of subsequent therapy initiation. Conclusions: Failure to initiate subsequent therapy after first-line discontinuation was not uncommon in real-world practice, but its interpretation depended on the denominator definition and treatment context. In the immune checkpoint inhibitor era, lower rates of subsequent therapy initiation may not have the same clinical implications as in the TKI monotherapy era and should be interpreted cautiously.
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